NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM823828 Query DataSets for GSM823828
Status Public on Feb 29, 2012
Title Array 15_IVP rep2
Sample type RNA
 
Channel 1
Source name in vivo control blastocyst
Organism Bos taurus
Characteristics sample type: in_vivo
breed (cattle): Simmental
reproductive status (cattle): Heifer
Extracted molecule total RNA
Extraction protocol Total RNA extraction was performed using the PicoPure RNA Isolation Kit (ARCTURS, Munich, Germany) according to the manufacturer's instruction.
Label Cy5
Label protocol Amplification of RNA has been done using the RiboAmpb HSPlus RNA Amplification kit (Molecular devices). This procedure may be required for microarray experiments with extremely limited amounts of starting material. The RiboAmpb HSPlus RNA Amplification Kit enables the production of microgram quantities of antisense RNA (aRNA) from picogram quantities of total cellular RNA. The RiboAmpb HSPlus Kit achieves high yields of aRNA with a proprietary linear amplification process using double-stranded cDNA as template in a two round T7 RNA polymerase catalyzed amplification.
Labelling aRNA was performed using the Universal Linkage System (ULS) by Kreatech for Gene Expression studies using microarray slides from Agilent. ULS is a non-enzymatic protocol that allows direct labeling of unmodified, amplified RNA. ULS will react with unmodified, amplified RNA and label it by formation of a coordinative bond on the N7 position of guanine. Fluorophore Cy3 and Cy5 are linked via a spacer to the ULS molecule.
 
Channel 2
Source name in vitro produced blastocyst
Organism Bos taurus
Characteristics sample type: in_vitro
breed (cattle): N/A
reproductive status (cattle): N/A
Extracted molecule total RNA
Extraction protocol Total RNA extraction was performed using the PicoPure RNA Isolation Kit (ARCTURS, Munich, Germany) according to the manufacturer's instruction.
Label Cy3
Label protocol Amplification of RNA has been done using the RiboAmpb HSPlus RNA Amplification kit (Molecular devices). This procedure may be required for microarray experiments with extremely limited amounts of starting material. The RiboAmpb HSPlus RNA Amplification Kit enables the production of microgram quantities of antisense RNA (aRNA) from picogram quantities of total cellular RNA. The RiboAmpb HSPlus Kit achieves high yields of aRNA with a proprietary linear amplification process using double-stranded cDNA as template in a two round T7 RNA polymerase catalyzed amplification.
Labelling aRNA was performed using the Universal Linkage System (ULS) by Kreatech for Gene Expression studies using microarray slides from Agilent. ULS is a non-enzymatic protocol that allows direct labeling of unmodified, amplified RNA. ULS will react with unmodified, amplified RNA and label it by formation of a coordinative bond on the N7 position of guanine. Fluorophore Cy3 and Cy5 are linked via a spacer to the ULS molecule.
 
 
Hybridization protocol A total of 825 ng of each labeled sample were incubated in a solution containing 2X blocking agent and 1X fragmentation buffer in a volume of 55 μl at 65 °C for 15 min, and were then put on ice. Fifty-five microliters of 2X GEx Hybridization Buffer HI-RPM was added for a final volume of 110 μl. The hybridization mix was added onto the array and hybridization was performed at 65 °C for 17 hr using an Agilent Hybridization chamber in a rotating oven
Scan protocol Slides were scanned using Agilent’s High-Resolution C Scanner (Agilent Technologies, CA, USA) and features were extracted with the Agilent's Feature Extraction software (Agilent Technologies, CA, USA).
Description Array 15
Data processing Data were submitted to a simple background correction, a Loess within array normalization and a Quantile between array normalization.
 
Submission date Oct 28, 2011
Last update date Feb 29, 2012
Contact name Ahmed Gad
E-mail(s) [email protected]
Organization name Colorado State University
Department Biomedical Sciences
Lab ARBL
Street address 3107 Rampart Rd
City Fort Collins
State/province Colorado
ZIP/Postal code 80521
Country USA
 
Platform ID GPL13226
Series (1)
GSE33314 Gene expression analysis of bovine blastocyst produced under alternative in vivo and in vitro culture conditions during EGA time

Data table header descriptions
ID_REF
VALUE Normalized log2 ratio representing test/reference
INV_VALUE Normalized log2 ratio (Cy5/Cy3) representing reference/test

Data table
ID_REF VALUE INV_VALUE
EMBV3_00001 1.16729 -1.167293912
EMBV3_00002 0.225799 -0.225799255
EMBV3_00003 0.43439 -0.434389538
EMBV3_00004 0.438246 -0.438245586
EMBV3_00005 -0.0896425 0.089642457
EMBV3_00006 0.762919 -0.762918625
EMBV3_00007 -0.161363 0.161363236
EMBV3_00008 0.33065 -0.330649754
EMBV3_00009 -0.274652 0.274651598
EMBV3_00010 0.0715927 -0.071592677
EMBV3_00011 -0.244704 0.244704138
EMBV3_00012 -0.460553 0.460553414
EMBV3_00013 0.428196 -0.428195959
EMBV3_00014 -0.507599 0.507598699
EMBV3_00015 0.517023 -0.51702263
EMBV3_00016 -0.0189662 0.018966206
EMBV3_00017 -0.405044 0.405043662
EMBV3_00018 0.673446 -0.673446393
EMBV3_00019 0.224762 -0.224762149
EMBV3_00020 1.07424 -1.074244029

Total number of rows: 43794

Table truncated, full table size 1451 Kbytes.




Supplementary file Size Download File type/resource
GSM823828_K2_3.txt.gz 11.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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