|
Status |
Public on Feb 25, 2021 |
Title |
Cd4CrePofut1_WT 2 |
Sample type |
RNA |
|
|
Source name |
empty vector-transduced WT P14 cells at day 7.5 post-infection from spleen
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 transduction: empty vector genotype/variation: WT
|
Treatment protocol |
Sorted cells were lysed with lysis buffer from Rneasy Micro kit from Qiagen.
|
Growth protocol |
WT or Pofut1-null P14 cells with or without NICD co-expression were sorted from spleen after LCMV-Armstrong infection.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA samples were prepared according to the prototol of Rneasy Micro kit from Qiagen,
|
Label |
biotin
|
Label protocol |
Total RNA (1 - 20 ng) were converted into biotinylated cDNA using the NuGEN WTA Pico v2 protocol and the NuGEN Encore Biotin module
|
|
|
Hybridization protocol |
Six micrograms of biotinylated cDNA was fragmented and then hybridized for 16 hr at 45C on an Affymetrix Clariom S mouse GeneChip. Following hybridization, GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
|
Scan protocol |
GeneChips were scanned using the AffymetrixGeneChip Scanner 3000 7G.
|
Data processing |
Probe signals were quantile normalized and summarized by the RMA algorithm using the Affymetrix Expression Console software v1.1
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|
|
Submission date |
Oct 27, 2020 |
Last update date |
Feb 27, 2021 |
Contact name |
Hongbo Chi |
E-mail(s) |
hongbo.chi@stjude.org
|
Organization name |
St Jude Children's Research Hospital
|
Department |
Immunology
|
Street address |
262 Danny Thomas Place
|
City |
Memphis |
State/province |
TN |
ZIP/Postal code |
38105 |
Country |
USA |
|
|
Platform ID |
GPL23038 |
Series (2) |
GSE160225 |
In vivo CRISPR screening reveals nutrient signaling processes underpinning CD8+ T cell fate decisions [Pofut1_microarray] |
GSE160341 |
In vivo CRISPR screening reveals nutrient signaling processes underpinning CD8+ T cell fate decisions |
|