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Sample GSM1049713 Query DataSets for GSM1049713
Status Public on Dec 06, 2012
Title Cultured GRK2-expressing HEK cell clone-rep2
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-2
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 170.645 P 0.000753643
AFFX-BioB-M_at 215.349 P 0.000753643
AFFX-BioB-3_at 133.322 P 0.000581214
AFFX-BioC-5_at 496.29 P 0.000753643
AFFX-BioC-3_at 653.235 P 4.42873e-05
AFFX-BioDn-5_at 1099.08 P 4.42873e-05
AFFX-BioDn-3_at 2213.86 P 0.000581214
AFFX-CreX-5_at 6437 P 5.16732e-05
AFFX-CreX-3_at 6976.84 P 4.42873e-05
AFFX-DapX-5_at 38.7803 P 0.000662269
AFFX-DapX-M_at 87.1712 P 0.00227496
AFFX-DapX-3_at 118.823 P 0.000753643
AFFX-LysX-5_at 10.0601 A 0.41138
AFFX-LysX-M_at 10.7249 A 0.52976
AFFX-LysX-3_at 18.3492 P 0.00110197
AFFX-PheX-5_at 5.46681 A 0.645547
AFFX-PheX-M_at 9.31498 A 0.455413
AFFX-PheX-3_at 9.88752 A 0.39692
AFFX-ThrX-5_at 17.1137 A 0.275146
AFFX-ThrX-M_at 17.1045 A 0.108979

Total number of rows: 54675

Table truncated, full table size 1639 Kbytes.




Supplementary file Size Download File type/resource
GSM1049713_HEK-GRK-2.CEL.gz 5.4 Mb (ftp)(http) CEL
GSM1049713_HEK-GRK-2.CHP.gz 295.4 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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