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Sample GSM1049712 Query DataSets for GSM1049712
Status Public on Dec 06, 2012
Title Cultured GRK2-expressing HEK cell clone-rep1
Sample type RNA
 
Source name Cultured HEK cell clone with GRK2 expression
Organism Homo sapiens
Characteristics cell type: HEK cell clones
genotype/variation: GRK2
protocol: cultured in vitro
Treatment protocol For the microarray study, cell pellets were isolated from three study groups: (i) NOD.Scid mouse-expanded HEK clones expressing either GRK2 or kinase-deficient GRK2-K220R (Scid), (ii) in vitro cultured HEK cell clones expressing GRK2 or GRK2-K220R (HEK), and (iii) in vitro re-cultured HEK cell clones after NOD.Scid mouse expansion (Ex-Scid).
Growth protocol The study was performed with HEK cell clones stably expressing GRK2 or the kinase-deficient GRK2-K220R mutant. HEK cell clones were either expanded for 4 weeks in vivo in immunodeficient NOD.Scid mice (3 months of age), cultured in vitro, or re-cultured in vitro after expansion in NOD.Scid mice
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from HEK cell clones with the RNeasy Mini kit according to the manufacturer`s instructions (Qiagen).
Label biotin
Label protocol Biotinylated cRNA was prepared according to the protocol of the manufacturer (Affymetrix; GeneChip Expression Analysis Technical Manual).
 
Hybridization protocol For hybridization, 15 µg of fragmented cRNA were incubated with the chip (Affymetrix Human genome U133 Plus 2.0 Array) in 200 µl of the hybrization solution in a Hybridization Oven 640 (Affymetrix) for 16 h at 45 °C. GeneChips were then washed and stained using the Affymetrix Fluidics Station 450 according to the GeneChip Expression Analysis Technical Manual (Rev. 5).
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 7G.
Description HEK-GRK-1
Cultured GRK2-expressing HEK cell clone
Gene expression data of cultured GRK2-expressing HEK cell clone
Data processing The signals were processed using Affymetrix GeneChip Operating Software (GCOS; v.1.4; Affymetrix). To compare samples and experiments, the trimmed mean signal of each array was scaled to a target intensity of 200.
 
Submission date Dec 06, 2012
Last update date Dec 06, 2012
Contact name Ursula Quitterer
E-mail(s) [email protected]
Phone +41-446329801
Organization name ETH Zurich
Department Molecular Pharmacology
Street address Winterthurerstrasse 190
City Zurich
ZIP/Postal code CH-8057
Country Switzerland
 
Platform ID GPL570
Series (1)
GSE42771 Microarray gene expression profiling of kinase-dependent and kinase-independent effects of GRK2

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 161.678 P 0.000856509
AFFX-BioB-M_at 223.659 P 0.000972149
AFFX-BioB-3_at 120.968 P 0.000662269
AFFX-BioC-5_at 524.049 P 0.000753643
AFFX-BioC-3_at 546.615 P 4.42873e-05
AFFX-BioDn-5_at 1106.55 P 4.42873e-05
AFFX-BioDn-3_at 2212.17 P 0.000509415
AFFX-CreX-5_at 6386.72 P 5.16732e-05
AFFX-CreX-3_at 7013.26 P 4.42873e-05
AFFX-DapX-5_at 36.9239 P 0.000509415
AFFX-DapX-M_at 91.0373 P 0.00227496
AFFX-DapX-3_at 112.34 P 0.000972149
AFFX-LysX-5_at 7.60556 A 0.083592
AFFX-LysX-M_at 7.40134 A 0.39692
AFFX-LysX-3_at 29.9822 P 0.000662269
AFFX-PheX-5_at 1.44251 A 0.804734
AFFX-PheX-M_at 2.34795 A 0.834139
AFFX-PheX-3_at 15.8815 A 0.313723
AFFX-ThrX-5_at 15.9123 A 0.425962
AFFX-ThrX-M_at 22.9047 P 0.00933744

Total number of rows: 54675

Table truncated, full table size 1642 Kbytes.




Supplementary file Size Download File type/resource
GSM1049712_HEK-GRK-1.CEL.gz 5.4 Mb (ftp)(http) CEL
GSM1049712_HEK-GRK-1.CHP.gz 295.6 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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