Search results for the GEO ID: GSE3419 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM77091 | GPL96 |
|
Human Hair Follicle Bulge#1
|
Human scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
per Affymetrix protocol
|
Sample_geo_accession | GSM77091
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MAS v5
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77091/suppl/GSM77091.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77091 | GPL96 |
|
Human Hair Follicle Bulge#1
|
Human scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
per Affymetrix protocol
|
Sample_geo_accession | GSM77091
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MAS v5
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77091/suppl/GSM77091.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77092 | GPL96 |
|
Human Hair Follicle Sub-Bulge#1
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77092
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77092/suppl/GSM77092.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77092 | GPL96 |
|
Human Hair Follicle Sub-Bulge#1
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77092
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77092/suppl/GSM77092.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77093 | GPL96 |
|
Human Hair Follicle Bulge#2
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77093
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77093/suppl/GSM77093.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77093 | GPL96 |
|
Human Hair Follicle Bulge#2
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77093
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77093/suppl/GSM77093.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77094 | GPL96 |
|
Human Hair Follicle Sub-bulge#2
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77094
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77094/suppl/GSM77094.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77094 | GPL96 |
|
Human Hair Follicle Sub-bulge#2
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77094
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77094/suppl/GSM77094.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77095 | GPL96 |
|
Human Hair Follicle Bulge#3
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77095
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77095/suppl/GSM77095.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77095 | GPL96 |
|
Human Hair Follicle Bulge#3
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77095
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77095/suppl/GSM77095.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77096 | GPL96 |
|
Human Hair Follicle Sub-bulge#3
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77096
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77096/suppl/GSM77096.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77096 | GPL96 |
|
Human Hair Follicle Sub-bulge#3
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77096
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77096/suppl/GSM77096.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77097 | GPL96 |
|
Human Hair Follicle Bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77097
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77097/suppl/GSM77097.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77097 | GPL96 |
|
Human Hair Follicle Bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77097
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77097/suppl/GSM77097.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77098 | GPL96 |
|
Human Hair Follicle Sub-bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77098
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77098/suppl/GSM77098.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77098 | GPL96 |
|
Human Hair Follicle Sub-bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77098
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77098/suppl/GSM77098.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77099 | GPL96 |
|
Human Hair Follicle Upper-Bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77099
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77099/suppl/GSM77099.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77099 | GPL96 |
|
Human Hair Follicle Upper-Bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77099
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77099/suppl/GSM77099.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77100 | GPL96 |
|
Human Hair Follicle Inner-Bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77100
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77100/suppl/GSM77100.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77100 | GPL96 |
|
Human Hair Follicle Inner-Bulge#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77100
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77100/suppl/GSM77100.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77101 | GPL96 |
|
Human Hair Follicle Suprabulbar#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77101
| Sample_status | Public on Dec 08 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77101/suppl/GSM77101.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77101 | GPL96 |
|
Human Hair Follicle Suprabulbar#4
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77101
| Sample_status | Public on Dec 08 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77101/suppl/GSM77101.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77102 | GPL96 |
|
Human Hair Follicle Bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77102
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77102/suppl/GSM77102.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77102 | GPL96 |
|
Human Hair Follicle Bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77102
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77102/suppl/GSM77102.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77103 | GPL96 |
|
Human Hair Follicle Sub-bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77103
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77103/suppl/GSM77103.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77103 | GPL96 |
|
Human Hair Follicle Sub-bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77103
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77103/suppl/GSM77103.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77104 | GPL96 |
|
Human Hair Follicle Upper-Bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77104
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77104/suppl/GSM77104.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77104 | GPL96 |
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Human Hair Follicle Upper-Bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77104
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77104/suppl/GSM77104.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77105 | GPL96 |
|
Human Hair Follicle Inner-Bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77105
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77105/suppl/GSM77105.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77105 | GPL96 |
|
Human Hair Follicle Inner-Bulge#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77105
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77105/suppl/GSM77105.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77106 | GPL96 |
|
Human Hair Follicle Suprabulbar#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77106
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77106/suppl/GSM77106.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
|
GSM77106 | GPL96 |
|
Human Hair Follicle Suprabulbar#5
|
Human Scalp
|
Transverse frozen sections of human scalp were made. After precisely defining the different anatomical locations of individual hair follicles, laser capture microdissection was used to isolate the desired hair follicle cells.
|
Affymetrix protocol
|
Sample_geo_accession | GSM77106
| Sample_status | Public on Dec 06 2005
| Sample_submission_date | Oct 06 2005
| Sample_last_update_date | Oct 06 2005
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Picopure RNA isolation kit (Arcturas) and DNAse digestion (Qiagen)
| Sample_extract_protocol_ch1 |
| Sample_extract_protocol_ch1 | Quality assessed by Agilent 2100 bioanalyzer and a RNA 6000 Pico LabChip kit (Agilent)
| Sample_label_ch1 | Biotin
| Sample_label_protocol_ch1 | T7-primer based two round linear RNA amplification protocol: "Genechip Eukaryotic Small Sample Target Labeling Assay Version II" (equivalent to the GeneChip Two-Cycle cDNA Synthesis kit, Affymetrix)
| Sample_data_processing | MASv5.0
| Sample_platform_id | GPL96
| Sample_contact_name | Jonathan,,Vogel
| Sample_contact_email | jonvogel@mail.nih.gov
| Sample_contact_phone | 301 496-9002
| Sample_contact_department | Dermatology
| Sample_contact_institute | National Cancer Institute; NIH
| Sample_contact_address | Bldg. 10 / Room 12N260
| Sample_contact_city | Bethesda
| Sample_contact_state | MD
| Sample_contact_zip/postal_code | 20892-1908
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM77nnn/GSM77106/suppl/GSM77106.CEL.gz
| Sample_series_id | GSE3419
| Sample_data_row_count | 22283
| |
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Make groups for comparisons |
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Select GSMs and click on "Add groups" |
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