Search results for the GEO ID: GSE17995 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM450397 | GPL339 |
|
syngen transplanted C57BL/6 mice
|
syngen transplanted C57BL/6 mice
|
strain: C57BL/6
age: 9-12 weeks old
gender: female
cell type: splenocytes
|
syngen transplanted C57BL/6 mice
|
Sample_geo_accession | GSM450397
| Sample_status | Public on Sep 14 2009
| Sample_submission_date | Sep 07 2009
| Sample_last_update_date | Sep 09 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | B6 recipients were irradiated with 10.0 Gray, administered from a 137 Cs source. Splenocytes from B6 mice were prepared as single cell suspensions in PBS and depleted of red blood cells. 2 – 3 × 10^7 splenocytes in a volume of 200 μl were transplanted into B6 recipients via tail vein injection 4 – 6 h after irradiation. Mouse splenocytes were collected on day 4 after transplantation.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared with acid phenol/chloroform extraction (TRIzol, Invitrogen; Karlsruhe, Germany) followed by purification with RNeasy Mini Kit (Qiagen; Hilden, Germany) according to the manufacturer’s instructions and was quantified spectro-photometrically. The quality of the purified RNA was assessed by agarose gel analysis.
| Sample_label_ch1 | biotin, streptavidin-phycoerytrin
| Sample_label_protocol_ch1 | A total of 10 µg RNA from each sample was used to prepare biotinylated target cRNA as previously described (Staege MS, Hutter C, Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res 2004;64:8213-21). A detailed protocol is available at www.affymetrix.com.
| Sample_hyb_protocol | standard Affymetrix protocol
| Sample_scan_protocol | standard Affymetrix protocol
| Sample_data_processing | Microarray Suite 5.0 was used with the data and for normalization by scaling all probe sets to 500.
| Sample_platform_id | GPL339
| Sample_contact_name | Guenther,HS,Richter
| Sample_contact_email | guenther.richter@lrz.tum.de
| Sample_contact_fax | +49-89-3068 3791
| Sample_contact_laboratory | Laboratory f. Functional Genomics & Transplantation Biology
| Sample_contact_department | Pediatrics & Children's Cancer Research Center
| Sample_contact_institute | Klinikum rechts der Isar, TU-Muenchen
| Sample_contact_address | Parzivalstr. 16
| Sample_contact_city | Munich
| Sample_contact_zip/postal_code | D-80804
| Sample_contact_country | Germany
| Sample_contact_web_link | http://www.kind.med.tu-muenchen.de/cms/front_content.php
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450397/suppl/GSM450397.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450397/suppl/GSM450397.CHP.gz
| Sample_series_id | GSE17995
| Sample_data_row_count | 22690
| |
|
GSM450398 | GPL339 |
|
allogeneic transplanted, isotype treated mice, sample 1
|
allogeneic transplanted C57BL/6 mice, isotype treated
|
strain recipient: C57BL/6
strain donor: C3H/HeN
age: 9-12 weeks old
gender: female
cell type: splenocytes
|
allogeneic transplanted C57BL/6 mice, isotype treated
|
Sample_geo_accession | GSM450398
| Sample_status | Public on Sep 14 2009
| Sample_submission_date | Sep 07 2009
| Sample_last_update_date | Sep 09 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | B6 recipients were irradiated with 10.0 Gray, administered from a 137 Cs source. Splenocytes from C3H mice were prepared as single cell suspensions in PBS and depleted of red blood cells. 2 – 3 × 10^7 splenocytes in a volume of 200 μl were transplanted into B6 recipients via tail vein injection 4 – 6 h after irradiation. Mice were treated with isotype control (control rat IgG). Mouse splenocytes were collected on day 4 after transplantation.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared with acid phenol/chloroform extraction (TRIzol, Invitrogen; Karlsruhe, Germany) followed by purification with RNeasy Mini Kit (Qiagen; Hilden, Germany) according to the manufacturer’s instructions and was quantified spectro-photometrically. The quality of the purified RNA was assessed by agarose gel analysis.
| Sample_label_ch1 | biotin, streptavidin-phycoerytrin
| Sample_label_protocol_ch1 | A total of 10 µg RNA from each sample was used to prepare biotinylated target cRNA as previously described (Staege MS, Hutter C, Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res 2004;64:8213-21). A detailed protocol is available at www.affymetrix.com.
| Sample_hyb_protocol | standard Affymetrix protocol
| Sample_scan_protocol | standard Affymetrix protocol
| Sample_data_processing | Microarray Suite 5.0 was used with the data and for normalization by scaling all probe sets to 500.
| Sample_platform_id | GPL339
| Sample_contact_name | Guenther,HS,Richter
| Sample_contact_email | guenther.richter@lrz.tum.de
| Sample_contact_fax | +49-89-3068 3791
| Sample_contact_laboratory | Laboratory f. Functional Genomics & Transplantation Biology
| Sample_contact_department | Pediatrics & Children's Cancer Research Center
| Sample_contact_institute | Klinikum rechts der Isar, TU-Muenchen
| Sample_contact_address | Parzivalstr. 16
| Sample_contact_city | Munich
| Sample_contact_zip/postal_code | D-80804
| Sample_contact_country | Germany
| Sample_contact_web_link | http://www.kind.med.tu-muenchen.de/cms/front_content.php
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450398/suppl/GSM450398.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450398/suppl/GSM450398.CHP.gz
| Sample_series_id | GSE17995
| Sample_data_row_count | 22690
| |
|
GSM450399 | GPL339 |
|
allogeneic transplanted, isotype treated mice, sample 2
|
allogeneic transplanted C57BL/6 mice, isotype treated
|
strain recipient: C57BL/6
strain donor: C3H/HeN
age: 9-12 weeks old
gender: female
cell type: splenocytes
|
allogeneic transplanted C57BL/6 mice, isotype treated
|
Sample_geo_accession | GSM450399
| Sample_status | Public on Sep 14 2009
| Sample_submission_date | Sep 07 2009
| Sample_last_update_date | Sep 09 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | B6 recipients were irradiated with 10.0 Gray, administered from a 137 Cs source. Splenocytes from C3H mice were prepared as single cell suspensions in PBS and depleted of red blood cells. 2 – 3 × 10^7 splenocytes in a volume of 200 μl were transplanted into B6 recipients via tail vein injection 4 – 6 h after irradiation. Mice were treated with isotype control (control rat IgG). Mouse splenocytes were collected on day 4 after transplantation.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared with acid phenol/chloroform extraction (TRIzol, Invitrogen; Karlsruhe, Germany) followed by purification with RNeasy Mini Kit (Qiagen; Hilden, Germany) according to the manufacturer’s instructions and was quantified spectro-photometrically. The quality of the purified RNA was assessed by agarose gel analysis.
| Sample_label_ch1 | biotin, streptavidin-phycoerytrin
| Sample_label_protocol_ch1 | A total of 10 µg RNA from each sample was used to prepare biotinylated target cRNA as previously described (Staege MS, Hutter C, Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res 2004;64:8213-21). A detailed protocol is available at www.affymetrix.com.
| Sample_hyb_protocol | standard Affymetrix protocol
| Sample_scan_protocol | standard Affymetrix protocol
| Sample_data_processing | Microarray Suite 5.0 was used with the data and for normalization by scaling all probe sets to 500.
| Sample_platform_id | GPL339
| Sample_contact_name | Guenther,HS,Richter
| Sample_contact_email | guenther.richter@lrz.tum.de
| Sample_contact_fax | +49-89-3068 3791
| Sample_contact_laboratory | Laboratory f. Functional Genomics & Transplantation Biology
| Sample_contact_department | Pediatrics & Children's Cancer Research Center
| Sample_contact_institute | Klinikum rechts der Isar, TU-Muenchen
| Sample_contact_address | Parzivalstr. 16
| Sample_contact_city | Munich
| Sample_contact_zip/postal_code | D-80804
| Sample_contact_country | Germany
| Sample_contact_web_link | http://www.kind.med.tu-muenchen.de/cms/front_content.php
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450399/suppl/GSM450399.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450399/suppl/GSM450399.CHP.gz
| Sample_series_id | GSE17995
| Sample_data_row_count | 22690
| |
|
GSM450400 | GPL339 |
|
allogeneic transplanted, anti-ICOSL mAb day 0 treated mice, sample 1
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 0 treated
|
strain recipient: C57BL/6
strain donor: C3H/HeN
age: 9-12 weeks old
gender: female
cell type: splenocytes
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 0 treated
|
Sample_geo_accession | GSM450400
| Sample_status | Public on Sep 14 2009
| Sample_submission_date | Sep 07 2009
| Sample_last_update_date | Sep 09 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | B6 recipients were irradiated with 10.0 Gray, administered from a 137 Cs source. Splenocytes from C3H mice were prepared as single cell suspensions in PBS and depleted of red blood cells. 2 – 3 × 10^7 splenocytes in a volume of 200 μl were transplanted into B6 recipients via tail vein injection 4 – 6 h after irradiation. Mice received 500 μg anti-ICOSL mAb i. p starting at day 0, followed by subsequent injections of 200 μg of mAb every other day. Mouse splenocytes were collected on day 4 after transplantation.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared with acid phenol/chloroform extraction (TRIzol, Invitrogen; Karlsruhe, Germany) followed by purification with RNeasy Mini Kit (Qiagen; Hilden, Germany) according to the manufacturer’s instructions and was quantified spectro-photometrically. The quality of the purified RNA was assessed by agarose gel analysis.
| Sample_label_ch1 | biotin, streptavidin-phycoerytrin
| Sample_label_protocol_ch1 | A total of 10 µg RNA from each sample was used to prepare biotinylated target cRNA as previously described (Staege MS, Hutter C, Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res 2004;64:8213-21). A detailed protocol is available at www.affymetrix.com.
| Sample_hyb_protocol | standard Affymetrix protocol
| Sample_scan_protocol | standard Affymetrix protocol
| Sample_data_processing | Microarray Suite 5.0 was used with the data and for normalization by scaling all probe sets to 500.
| Sample_platform_id | GPL339
| Sample_contact_name | Guenther,HS,Richter
| Sample_contact_email | guenther.richter@lrz.tum.de
| Sample_contact_fax | +49-89-3068 3791
| Sample_contact_laboratory | Laboratory f. Functional Genomics & Transplantation Biology
| Sample_contact_department | Pediatrics & Children's Cancer Research Center
| Sample_contact_institute | Klinikum rechts der Isar, TU-Muenchen
| Sample_contact_address | Parzivalstr. 16
| Sample_contact_city | Munich
| Sample_contact_zip/postal_code | D-80804
| Sample_contact_country | Germany
| Sample_contact_web_link | http://www.kind.med.tu-muenchen.de/cms/front_content.php
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450400/suppl/GSM450400.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450400/suppl/GSM450400.CHP.gz
| Sample_series_id | GSE17995
| Sample_data_row_count | 22690
| |
|
GSM450401 | GPL339 |
|
allogeneic transplanted, anti-ICOSL mAb day 0 treated mice, sample 2
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 0 treated
|
strain recipient: C57BL/6
strain donor: C3H/HeN
age: 9-12 weeks old
gender: female
cell type: splenocytes
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 0 treated
|
Sample_geo_accession | GSM450401
| Sample_status | Public on Sep 14 2009
| Sample_submission_date | Sep 07 2009
| Sample_last_update_date | Sep 09 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | B6 recipients were irradiated with 10.0 Gray, administered from a 137 Cs source. Splenocytes from C3H mice were prepared as single cell suspensions in PBS and depleted of red blood cells. 2 – 3 × 10^7 splenocytes in a volume of 200 μl were transplanted into B6 recipients via tail vein injection 4 – 6 h after irradiation. Mice received 500 μg anti-ICOSL mAb i. p starting at day 0, followed by subsequent injections of 200 μg of mAb every other day. Mouse splenocytes were collected on day 4 after transplantation.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared with acid phenol/chloroform extraction (TRIzol, Invitrogen; Karlsruhe, Germany) followed by purification with RNeasy Mini Kit (Qiagen; Hilden, Germany) according to the manufacturer’s instructions and was quantified spectro-photometrically. The quality of the purified RNA was assessed by agarose gel analysis.
| Sample_label_ch1 | biotin, streptavidin-phycoerytrin
| Sample_label_protocol_ch1 | A total of 10 µg RNA from each sample was used to prepare biotinylated target cRNA as previously described (Staege MS, Hutter C, Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res 2004;64:8213-21). A detailed protocol is available at www.affymetrix.com.
| Sample_hyb_protocol | standard Affymetrix protocol
| Sample_scan_protocol | standard Affymetrix protocol
| Sample_data_processing | Microarray Suite 5.0 was used with the data and for normalization by scaling all probe sets to 500.
| Sample_platform_id | GPL339
| Sample_contact_name | Guenther,HS,Richter
| Sample_contact_email | guenther.richter@lrz.tum.de
| Sample_contact_fax | +49-89-3068 3791
| Sample_contact_laboratory | Laboratory f. Functional Genomics & Transplantation Biology
| Sample_contact_department | Pediatrics & Children's Cancer Research Center
| Sample_contact_institute | Klinikum rechts der Isar, TU-Muenchen
| Sample_contact_address | Parzivalstr. 16
| Sample_contact_city | Munich
| Sample_contact_zip/postal_code | D-80804
| Sample_contact_country | Germany
| Sample_contact_web_link | http://www.kind.med.tu-muenchen.de/cms/front_content.php
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450401/suppl/GSM450401.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450401/suppl/GSM450401.CHP.gz
| Sample_series_id | GSE17995
| Sample_data_row_count | 22690
| |
|
GSM450402 | GPL339 |
|
allogeneic transplanted, anti-ICOSL mAb day 3 treated mice, sample 1
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 3 treated
|
strain recipient: C57BL/6
strain donor: C3H/HeN
age: 9-12 weeks old
gender: female
cell type: splenocytes
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 3 treated
|
Sample_geo_accession | GSM450402
| Sample_status | Public on Sep 14 2009
| Sample_submission_date | Sep 07 2009
| Sample_last_update_date | Sep 09 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | B6 recipients were irradiated with 10.0 Gray, administered from a 137 Cs source. Splenocytes from C3H mice were prepared as single cell suspensions in PBS and depleted of red blood cells. 2 – 3 × 10^7 splenocytes in a volume of 200 μl were transplanted into B6 recipients via tail vein injection 4 – 6 h after irradiation. Mice received 500 μg anti-ICOSL mAb i. p starting at day 3, followed by subsequent injections of 200 μg of mAb every other day. Mouse splenocytes were collected on day 4 after transplantation.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared with acid phenol/chloroform extraction (TRIzol, Invitrogen; Karlsruhe, Germany) followed by purification with RNeasy Mini Kit (Qiagen; Hilden, Germany) according to the manufacturer’s instructions and was quantified spectro-photometrically. The quality of the purified RNA was assessed by agarose gel analysis.
| Sample_label_ch1 | biotin, streptavidin-phycoerytrin
| Sample_label_protocol_ch1 | A total of 10 µg RNA from each sample was used to prepare biotinylated target cRNA as previously described (Staege MS, Hutter C, Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res 2004;64:8213-21). A detailed protocol is available at www.affymetrix.com.
| Sample_hyb_protocol | standard Affymetrix protocol
| Sample_scan_protocol | standard Affymetrix protocol
| Sample_data_processing | Microarray Suite 5.0 was used with the data and for normalization by scaling all probe sets to 500.
| Sample_platform_id | GPL339
| Sample_contact_name | Guenther,HS,Richter
| Sample_contact_email | guenther.richter@lrz.tum.de
| Sample_contact_fax | +49-89-3068 3791
| Sample_contact_laboratory | Laboratory f. Functional Genomics & Transplantation Biology
| Sample_contact_department | Pediatrics & Children's Cancer Research Center
| Sample_contact_institute | Klinikum rechts der Isar, TU-Muenchen
| Sample_contact_address | Parzivalstr. 16
| Sample_contact_city | Munich
| Sample_contact_zip/postal_code | D-80804
| Sample_contact_country | Germany
| Sample_contact_web_link | http://www.kind.med.tu-muenchen.de/cms/front_content.php
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450402/suppl/GSM450402.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450402/suppl/GSM450402.CHP.gz
| Sample_series_id | GSE17995
| Sample_data_row_count | 22690
| |
|
GSM450403 | GPL339 |
|
allogeneic transplanted, anti-ICOSL mAb day 3 treated mice, sample 2
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 3 treated
|
strain recipient: C57BL/6
strain donor: C3H/HeN
age: 9-12 weeks old
gender: female
cell type: splenocytes
|
allogeneic transplanted C57BL/6 mice, anti-ICOSL mAb day 3 treated
|
Sample_geo_accession | GSM450403
| Sample_status | Public on Sep 14 2009
| Sample_submission_date | Sep 07 2009
| Sample_last_update_date | Sep 09 2009
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_treatment_protocol_ch1 | B6 recipients were irradiated with 10.0 Gray, administered from a 137 Cs source. Splenocytes from C3H mice were prepared as single cell suspensions in PBS and depleted of red blood cells. 2 – 3 × 10^7 splenocytes in a volume of 200 μl were transplanted into B6 recipients via tail vein injection 4 – 6 h after irradiation. Mice received 500 μg anti-ICOSL mAb i. p starting at day 3, followed by subsequent injections of 200 μg of mAb every other day. Mouse splenocytes were collected on day 4 after transplantation.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA was prepared with acid phenol/chloroform extraction (TRIzol, Invitrogen; Karlsruhe, Germany) followed by purification with RNeasy Mini Kit (Qiagen; Hilden, Germany) according to the manufacturer’s instructions and was quantified spectro-photometrically. The quality of the purified RNA was assessed by agarose gel analysis.
| Sample_label_ch1 | biotin, streptavidin-phycoerytrin
| Sample_label_protocol_ch1 | A total of 10 µg RNA from each sample was used to prepare biotinylated target cRNA as previously described (Staege MS, Hutter C, Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res 2004;64:8213-21). A detailed protocol is available at www.affymetrix.com.
| Sample_hyb_protocol | standard Affymetrix protocol
| Sample_scan_protocol | standard Affymetrix protocol
| Sample_data_processing | Microarray Suite 5.0 was used with the data and for normalization by scaling all probe sets to 500.
| Sample_platform_id | GPL339
| Sample_contact_name | Guenther,HS,Richter
| Sample_contact_email | guenther.richter@lrz.tum.de
| Sample_contact_fax | +49-89-3068 3791
| Sample_contact_laboratory | Laboratory f. Functional Genomics & Transplantation Biology
| Sample_contact_department | Pediatrics & Children's Cancer Research Center
| Sample_contact_institute | Klinikum rechts der Isar, TU-Muenchen
| Sample_contact_address | Parzivalstr. 16
| Sample_contact_city | Munich
| Sample_contact_zip/postal_code | D-80804
| Sample_contact_country | Germany
| Sample_contact_web_link | http://www.kind.med.tu-muenchen.de/cms/front_content.php
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450403/suppl/GSM450403.CEL.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM450nnn/GSM450403/suppl/GSM450403.CHP.gz
| Sample_series_id | GSE17995
| Sample_data_row_count | 22690
| |
|
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