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Sample GSM14592 Query DataSets for GSM14592
Status Public on Mar 27, 2004
Title Medial #2
Sample type RNA
 
Source name E16.5 mouse cortex
Organism Mus musculus
Extracted molecule total RNA
 
Description Dissection of E16.5 cortex for RNA extraction. Cortex Hemispheres of E16.5 mice were divided into the medial (R1), dorsal (R2), ventral (R3), lateral (R4), and occipital regions (R5). Preparation of RNA and Synthesis of cDNA. Poly A+ RNA was obtained through twice column procedures with oligo dT cellulose column (New England Biolabs, Beverly, MA) and was used for synthesis of cDNA. 1ug of polyA+ RNA was converted into double-stranded cDNA by reverse transcription using ReverTra Ace (ToYoBo, Japan) with oligo dT(24) primers containing the T7 RNA polymerase promotor sequence (Amersham Pharmacia Biotech, Japan). The integrity of RNA was confirmed by agarose electrophoresis and RNA contents were analyzed by measuring the optical density at 260 nm. Target preparation and array processing. The following procedures including preparation of cRNA targets, hybridization, washing, staining, and scanning were performed as described in the Expression Analysis Technical Manual (Affymetrix, CA). Briefly, biotin-labeled antisense cRNA targets were synthesized in in vitro transcription reaction system (IVT) using cDNA as template (ENZO BioArrayTM HighYieldTM RNA Transcription Labeling kit with T7 RNA polymerase, Enzo, NY). The cRNA targets were size-fragmented to 35-200 bp in a buffer containing potassium and magnesium acetate at 94 °C for 35 minutes and were used for hybridization as cRNA targets. The hybridization cocktail [containing 10 ug of target cRNA, control oligo BS (Affymetrix), and Eukaryotic Hybridization controls (Affymetrix)] was hybridized with a mouse U74A array at 42 °C for 16 hours in GeneChip Hybridization Oven 640. Washing and staining were performed after hybridization under the fluidics station protocol, EuGE-WS2, on GeneChip Fluidics Station 400. Then, we scanned the array twice on HP GeneArrayTM scanner. Experiments were repeated twice with independent dissection. Data analysis. To quantify the expression level of a transcript, the average difference value (Adv) was calculated from the intensities against the probe cells using the global methods of normalization by Microarray Suite ver. 4.0 (Affymetrix).
Keywords = mouse
Keywords = cortex
Keywords = development
Keywords = regional
Keywords = gene expression
Keywords = medial
Keywords = dorsal
Keywords = lateral
Keywords = rostral
Keywords = occipital
 
Submission date Dec 25, 2003
Last update date Oct 28, 2005
Contact name Nobuo Funatsu
E-mail(s) [email protected]
Phone 81-042-346-1722
Fax 81-042-346-1752
Organization name National Institute of Neuroscience, NCNP
Department Cellular Biology
Street address 4-1-1 Ogawahigashi
City Kodaira
State/province Tokyo
ZIP/Postal code 187-8502
Country Japan
 
Platform ID GPL81
Series (1)
GSE929 Gene expression analysis of the developing cortex

Data table header descriptions
ID_REF
VALUE Affymetrix MAS 4.0 A quantitative measure of the abundance of a transcript
ABS_CALL Affymetrix MAS 4.0 A quantitative measurement indicating if the transcript is present (P), absent (A), or marginal (M)

Data table
ID_REF VALUE ABS_CALL
AFFX-MurIL2_at -368.7 A
AFFX-MurIL10_at 93.7 A
AFFX-MurIL4_at 116.1 A
AFFX-MurFAS_at 211.4 A
AFFX-BioB-5_at 1953.7 P
AFFX-BioB-M_at 2559.4 P
AFFX-BioB-3_at 1812.6 P
AFFX-BioC-5_at 6042.7 P
AFFX-BioC-3_at 7484.9 P
AFFX-BioDn-5_at 7225.4 P
AFFX-BioDn-3_at 25251.6 P
AFFX-CreX-5_at 55857 P
AFFX-CreX-3_at 66891.1 P
AFFX-BioB-5_st 1365.3 A
AFFX-BioB-M_st -518 A
AFFX-BioB-3_st -1619.9 A
AFFX-BioC-5_st -1037.9 A
AFFX-BioC-3_st 5.8 A
AFFX-BioDn-5_st 1639.6 A
AFFX-BioDn-3_st 341.6 A

Total number of rows: 12488

Table truncated, full table size 224 Kbytes.




Supplementary data files not provided

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