|
Status |
Public on Feb 03, 2013 |
Title |
PC Blimp1-hi |
Sample type |
RNA |
|
|
Source name |
follicualr B cells
|
Organism |
Mus musculus |
Characteristics |
background strain: C57BL/6 cell type: follicualr B cells cell population: CD138+ Blimp1 high genotype/variation: prmd1-gfp
|
Treatment protocol |
FACS sorted, no external treatments.
|
Growth protocol |
Isolated ex vivo. No growth.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with Trizol reagent, followed by clean-up and DNase I treatment with QIAGEN RNeasy mini kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with Agilent Bioanalyser.
|
Label |
Cy3
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
|
|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Data processing |
The data were variance stabilised using lumiT and then quantile normalised using lumi package
|
|
|
Submission date |
Dec 31, 2012 |
Last update date |
Feb 03, 2013 |
Contact name |
David M Tarlinton |
E-mail(s) |
tarlinton@wehi.edu.au
|
Phone |
+61393452555
|
Fax |
+61393470852
|
Organization name |
WEHI
|
Street address |
1G Royal Pde
|
City |
Parkville |
State/province |
Vic |
ZIP/Postal code |
3052 |
Country |
Australia |
|
|
Platform ID |
GPL6333 |
Series (2) |
GSE43214 |
Plasma cells from spleen were FACS sorted using Blmp1 and CD138 expression and gene expression compared to naïve B cells, FACS sorted using B220 and IgD |
GSE43215 |
Gene expression changes during mouse plasma cell differentiation |
|