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Status |
Public on Apr 20, 2020 |
Title |
J3T1shA |
Sample type |
RNA |
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|
Source name |
J3T1shA
|
Organism |
Canis lupus familiaris |
Characteristics |
tissue: glioma subclone: J3T1shA expression: knockdown of annexin A2
|
Growth protocol |
Cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) with 10% fetal bovine serum and 100U penicillin and 0.1mg ml-1 storeptomycin.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA of J3T-1, J3T-2, J3T-1shA, and J3T2A were isolated using RNeasy kit according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were synthesized by GeneChip 3' IVT PLUS Reagent Kit from 250 ng total RNA according to the manufacturer's instructions.
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Hybridization protocol |
Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45˚C on GeneChip Canine Genome 2.0 Array. Arrays were washed and stained in the GeneChip Fluidics Station 450.
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Scan protocol |
Arrays were scanned using GeneChip Scanner 3000 7G.
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Description |
Gene expression data from J3T-1shA
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Data processing |
Single Array Analysis were calculated by Microarray Suite version 5.0 (MAS5.0) with Affymetrix default setting and global scaling as normalization method.
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Submission date |
Oct 03, 2019 |
Last update date |
Apr 20, 2020 |
Contact name |
Yuji Matsumoto |
Organization name |
Okayama University
|
Department |
Neurological Surgery
|
Street address |
2-5-1 Shikata, kita-ku
|
City |
Okayama |
ZIP/Postal code |
7008558 |
Country |
Japan |
|
|
Platform ID |
GPL3738 |
Series (1) |
GSE138374 |
Expression data of J3T-1, J3T-2, J3T-1shA, J3T-2A glioma |
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