NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM241227 Query DataSets for GSM241227
Status Public on Nov 10, 2007
Title cumulus cells-early cleavage-rep5
Sample type RNA
 
Source name cumulus cells from oocyte resulting in an early cleavage embryo (i.e. cleaved between 23-26h post-injection or 25-28h post-insemination) from patient 5
Organism Homo sapiens
Characteristics The oocyte enclosed by these cumulus cells was fertilized normally (2PN) and developed into a 4-cell embryo with good morphology on day 2 and no multinucleated blastomeres present.
Treatment protocol Cumulus cells were immediately lysed in 100 ml Trizol reagent (Invitrogen, Carlsbad, USA) supplemented with 1% (v/v) 2-mercapto-ethanol (Merck, Darmstadt, Germany), snap-frozen in liquid nitrogen and stored at -80°C (cumulus cells from one oocyte per vial).
Growth protocol In consenting IVF patients, immediately following ultrasound-guided cumulus-oocyte-complex (COC) retrieval, a proportion of the cumulus cells surrounding a single oocyte were removed using a sharp needle.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol reagent (Invitrogen, Carlsbad, USA) according to the manufacturers’ instructions with some adaptations for the small quantity of RNA. RNA was precipitated with isopropyl alcohol for 2h and the RNA pellet was washed three times with 75% ethanol. To be able to track the small RNA pellet, 5 mg glycogen (Ambion, Woodward, USA) was added to the sample before RNA precipitation.
Label biotin
Label protocol Fifty ng total RNA was amplified using the two-cycle cDNA synthesis kit (Affymetrix, Santa Clara, USA) in combination with the MEGAscript T7 in vitro transcription system (Ambion) and biotin labeled with GeneChip IVT labeling kit (Affymetrix).
 
Hybridization protocol Following fragmentation, 11 ug of cRNA were hybridized for 16 hr at 45C on Human Genome U133 Plus 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip scanner 3000 / 7G.
Description Comparison of cumulus cells from eight oocytes resulting in an early cleavage embryo (EC-CC; n=8) and from eight oocytes resulting in a non-EC embryo (NEC-CC; n=8).
Data processing Affymetrix GCOS, TGT value: 500, Norm Factor: 1
 
Submission date Nov 06, 2007
Last update date Aug 28, 2018
Contact name Aafke van Montfoort
E-mail(s) [email protected]
Organization name Academic hospital Maastricht
Department Obstetrics & Gynaecology
Lab IVF laboratory
Street address P.O.Box 5800
City maastricht
ZIP/Postal code 6202 AZ
Country Netherlands
 
Platform ID GPL570
Series (1)
GSE9526 Expression data from cumulus cells that surround oocytes resulting in early or late cleaving embryos
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE GCOS
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 2846 P 0.000754
AFFX-BioB-M_at 4131.1 P 0.000147
AFFX-BioB-3_at 3024.6 P 0.000044
AFFX-BioC-5_at 6382.9 P 0.00006
AFFX-BioC-3_at 7458 P 0.000044
AFFX-BioDn-5_at 16698.2 P 0.000044
AFFX-BioDn-3_at 29296.9 P 0.00006
AFFX-CreX-5_at 65124.1 P 0.000052
AFFX-CreX-3_at 73307 P 0.000044
AFFX-DapX-5_at 191.2 P 0.002556
AFFX-DapX-M_at 1938 P 0.000754
AFFX-DapX-3_at 5002.8 P 0.000044
AFFX-LysX-5_at 58.4 A 0.131361
AFFX-LysX-M_at 337.5 P 0.026111
AFFX-LysX-3_at 896.5 P 0.000044
AFFX-PheX-5_at 106.3 M 0.058444
AFFX-PheX-M_at 336.3 P 0.006187
AFFX-PheX-3_at 637.3 P 0.001248
AFFX-ThrX-5_at 74.2 A 0.354453
AFFX-ThrX-M_at 306.6 P 0.000754

Total number of rows: 54675

Table truncated, full table size 1442 Kbytes.




Supplementary file Size Download File type/resource
GSM241227.CEL.gz 4.9 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap