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Search results for the GEO ID: GSE7441
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GPL ID
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Title
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GSM178539
GPL1355
Primary rat spinal cord astrocytes NonTG-A Spinal cord astrocytes NonTG Primary spinal cord astrocytes from non-transgenic 1 day old rat littermates obtained from the breeding of a hSOD1G93A positive male with a negative female. Astrocytes were prepared as described in Cassina P, et al.J Neurosci Res. 2002;67(1):21-9. Transgenic hSOD1G93A rats were provided by D. S. Howland (Howland et al. 2002; PNAS, 99(3): 1604-1609) Labeling was done with the Affymetrix kits according to their one-cycle target labeling assay. Kits used were the one-cycle cDNA synthesis kit(900431), sample cleanup modules(900371), eukaryotic Poly-A RNA control kit (900433), IVT labeling kit(900449), Eukayotic hybridization control kit(900454) 5 ug of total RNA were used for the amplification. Hybridization, washing and scanning was done according to the Affymetrix protocol in GeneChip Expression Analysis Technical Manual 701021 Rev. 5.
GSM180126
GPL1355
Primary rat spinal cord astrocytes NonTG-B Spinal cord astrocytes NonTG Primary spinal cord astrocytes from non-transgenic 1 day old rat littermates obtained from the breeding of a hSOD1G93A positive male with a negative female. Astrocytes were prepared as described in Cassina P, et al.J Neurosci Res. 2002;67(1):21-9. Transgenic hSOD1G93A rats were provided by D. S. Howland (Howland et al. 2002; PNAS, 99(3): 1604-1609) Labeling was done with the Affymetrix kits according to their one-cycle target labeling assay. Kits used were the one-cycle cDNA synthesis kit(900431), sample cleanup modules(900371), eukaryotic Poly-A RNA control kit (900433), IVT labeling kit(900449), Eukayotic hybridization control kit(900454) 5 ug of total RNA were used for the amplification. Hybridization, washing and scanning was done according to the Affymetrix protocol in GeneChip Expression Analysis Technical Manual 701021 Rev. 5.
GSM180128
GPL1355
Primary rat spinal cord astrocytes NonTG-C Spinal cord astrocytes NonTG Primary spinal cord astrocytes from non-transgenic 1 day old rat littermates obtained from the breeding of a hSOD1G93A positive male with a negative female. Astrocytes were prepared as described in Cassina P, et al.J Neurosci Res. 2002;67(1):21-9. Transgenic hSOD1G93A rats were provided by D. S. Howland (Howland et al. 2002; PNAS, 99(3): 1604-1609) Labeling was done with the Affymetrix kits according to their one-cycle target labeling assay. Kits used were the one-cycle cDNA synthesis kit(900431), sample cleanup modules(900371), eukaryotic Poly-A RNA control kit (900433), IVT labeling kit(900449), Eukayotic hybridization control kit(900454) 5 ug of total RNA were used for the amplification. Hybridization, washing and scanning was done according to the Affymetrix protocol in GeneChip Expression Analysis Technical Manual 701021 Rev. 5.
GSM180130
GPL1355
Primary rat spinal cord astrocytes hSOD1G93A-A Spinal cord astrocytes from transgenic hSOD1G93A Primary spinal cord astrocytes from hSOD1G93A-transgenic 1 day old rat littermates obtained from the breeding of a hSOD1G93A positive male with a negative female. Astrocytes were prepared as described in Cassina P, et al.J Neurosci Res. 2002;67(1):21-9. Transgenic hSOD1G93A rats were provided by D. S. Howland (Howland et al. 2002; PNAS, 99(3): 1604-1609) Labeling was done with the Affymetrix kits according to their one-cycle target labeling assay. Kits used were the one-cycle cDNA synthesis kit(900431), sample cleanup modules(900371), eukaryotic Poly-A RNA control kit (900433), IVT labeling kit(900449), Eukayotic hybridization control kit(900454) 5 ug of total RNA were used for the amplification. Hybridization, washing and scanning was done according to the Affymetrix protocol in GeneChip Expression Analysis Technical Manual 701021 Rev. 5.
GSM180131
GPL1355
Primary rat spinal cord astrocytes hSOD1G93A-B Spinal cord astrocytes from transgenic hSOD1G93A Primary spinal cord astrocytes from hSOD1G93A-transgenic 1 day old rat littermates obtained from the breeding of a hSOD1G93A positive male with a negative female. Astrocytes were prepared as described in Cassina P, et al.J Neurosci Res. 2002;67(1):21-9. Transgenic hSOD1G93A rats were provided by D. S. Howland (Howland et al. 2002; PNAS, 99(3): 1604-1609) Labeling was done with the Affymetrix kits according to their one-cycle target labeling assay. Kits used were the one-cycle cDNA synthesis kit(900431), sample cleanup modules(900371), eukaryotic Poly-A RNA control kit (900433), IVT labeling kit(900449), Eukayotic hybridization control kit(900454) 5 ug of total RNA were used for the amplification. Hybridization, washing and scanning was done according to the Affymetrix protocol in GeneChip Expression Analysis Technical Manual 701021 Rev. 5.
GSM180175
GPL1355
Primary rat spinal cord astrocytes hSOD1G93A-C Spinal cord astrocytes from transgenic hSOD1G93A Primary spinal cord astrocytes from hSOD1G93A-transgenic 1 day old rat littermates obtained from the breeding of a hSOD1G93A positive male with a negative female. Astrocytes were prepared as described in Cassina P, et al.J Neurosci Res. 2002;67(1):21-9. Transgenic hSOD1G93A rats were provided by D. S. Howland (Howland et al. 2002; PNAS, 99(3): 1604-1609) Labeling was done with the Affymetrix kits according to their one-cycle target labeling assay. Kits used were the one-cycle cDNA synthesis kit(900431), sample cleanup modules(900371), eukaryotic Poly-A RNA control kit (900433), IVT labeling kit(900449), Eukayotic hybridization control kit(900454) 5 ug of total RNA were used for the amplification. Hybridization, washing and scanning was done according to the Affymetrix protocol in GeneChip Expression Analysis Technical Manual 701021 Rev. 5.
 
 
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