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Sample GSM630812 Query DataSets for GSM630812
Status Public on Nov 30, 2010
Title Anterior distal region of an E5.5 mouse embryo MOE430A rep1
Sample type RNA
 
Source name Anterior distal region of an E5.5 mouse embryo
Organism Mus musculus
Characteristics age: E5.5
tissue: Anterior distal region of embryo
genetic background: B6SJLF1×CerlP-GFP
Treatment protocol Embyos suffered no treatment prior to the extraction procedures
Growth protocol Embryos with fluorescently labeled AVE were collected from B6SJLF1×CerlP-GFP matings at 5.5 dpc.
Extracted molecule total RNA
Extraction protocol Ad and Pp regions were isolated from embryos in which the AVE occupied a lateraldistal position. For the isolation of Ad regions, fragments comprising the fluorescently labeled AVE and the underlying epiblast, were microdissected. Pp regions were isolated by dissecting triangular-shaped fragments of proximal visceral endoderm and epiblast from a position diametrically opposed to the fluorescently-labeled domain. The upper limit of the Pp fragments coincided with the embryonic-extraembryonic boundary and extended in depth to roughly one third of the diameter of the egg cylinder, while its lateral limit corresponded to about one third of the height of the embryonic region. The freshly dissected fragments were immediately homogenized with TRIzol® and frozen in liquid nitrogen. The samples were then stored at -80ºC until processing.
Label biotin
Label protocol A modified linear amplification protocol was applied to generate the required amount of probe, according to Van Gelder et al., 1990
 
Hybridization protocol 15 µg of biotinylated cRNA was used in a 300-µl hybridization containing added hybridization controls. 200 µl of mixture was hybridized on Affymetrix (Santa Clara, CA, USA) GeneChip Mouse Expression Set 430 arrays for 16 h at 45°C. Standard post hybridization wash and double-stain protocols were used on an Affymetrix GeneChip Fluidics Station 400.
Scan protocol Arrays were scanned on an Affymetrix GeneChip scanner 2500.
Description Gene expression data from Ad region of an E5.5 mouse embryo
Data processing Scanned arrays were analyzed first with Affymetrix MAS 5.0 software to obtain Absent/Present calls and for subsequent analysis with dChip 2010. Each set of 5 arrays (430A and 430B type) was analyzed separately from here on. Each set was normalized applying an Invariant Set Normalization Method. Then the normalized probe cell intensities of the 5 arrays were used to obtain model-based gene expression indices based on a PM-only model.
 
Submission date Nov 29, 2010
Last update date Nov 29, 2010
Contact name Lisa Goncalves
E-mail(s) [email protected]
Organization name CBME UALG
Street address Campus de Gambelas, Ed8, Lab 1.17
City Faro
ZIP/Postal code 8005
Country Portugal
 
Platform ID GPL339
Series (1)
GSE25675 Identification and functional analysis of novel genes expressed in the Anterior Visceral Endoderm

Data table header descriptions
ID_REF
VALUE dChip MBEI signal intensity.
ABS_CALL
A1_A SE

Data table
ID_REF VALUE ABS_CALL A1_A SE
AFFX-BioB-5_at 528.75 P 6.93
AFFX-BioB-M_at 484.33 P 4.98
AFFX-BioB-3_at 466.56 P 8.04
AFFX-BioC-5_at 1285.58 P 9.87
AFFX-BioC-3_at 998.71 P 8.50
AFFX-BioDn-5_at 834.43 P 6.64
AFFX-BioDn-3_at 3767.59 P 38.69
AFFX-CreX-5_at 7016.50 P 68.09
AFFX-CreX-3_at 11043.19 P 83.06
AFFX-DapX-5_at 101.28 A 1.46
AFFX-DapX-M_at 61.41 A 2.31
AFFX-DapX-3_at 137.35 A 5.45
AFFX-LysX-5_at 32.36 A 1.92
AFFX-LysX-M_at 125.80 A 3.84
AFFX-LysX-3_at 281.74 A 4.91
AFFX-PheX-5_at 137.05 A 5.39
AFFX-PheX-M_at 87.55 A 2.48
AFFX-PheX-3_at 254.76 A 4.03
AFFX-ThrX-5_at 234.24 A 3.56
AFFX-ThrX-M_at 108.19 A 2.59

Total number of rows: 22690

Table truncated, full table size 589 Kbytes.




Supplementary file Size Download File type/resource
GSM630812_Mm_embryo_A1_MOE430A_IGC5_JDB.CEL.gz 2.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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