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Sample GSM2193170 Query DataSets for GSM2193170
Status Public on Sep 01, 2016
Title CD4T_LG_rep1
Sample type RNA
 
Source name Lacrimal gland 16w NOD male
Organism Mus musculus
Characteristics tissue: lacrimal gland
subset: CD4T
Treatment protocol Lacrimal gland cell suspensions were prepared by mechanical dissociation and enzymatic digestion before FACS cell sorting of epithelial and immune cell subsets. Each cell subset was sorted directly into lysis buffer on a FACSAria cytometer (BD Biosciences). Lysates were stored at -80°C until processing.
Growth protocol cells were isolated ex vivo
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using RNAqueous isolation kit (Ambion). RNA was QC'd using Bioanayzer and all samples had RIN scores >8 except: SAMPLE 145 (RIN=7.8), SAMPLE 108 (RIN=7.7), SAMPLE 111 (RIN=7.2).
Label biotin
Label protocol The amount of isolated RNA was normalized and automated sample amplification and biotin labeling were carried out using the NuGEN Ovation RNA Amplification system V2, Ovation WB reagent and Encore Biotin module according to manufacturer’s recommendations using an Arrayplex automated liquid handler (Beckman Coulter).
 
Hybridization protocol Two micrograms of biotin labeled sscDNA probe were hybridized to Affymetrix GeneChip HT HG-U133+ PM plate arrays with modified conditions as described in (Allaire et al., 2013, PMID: 23289891). Washing and staining of the hybridized arrays were completed as described in the GeneChip Expression analysis technical manual for HT plate arrays using the Genechip Array Station (Affymetrix) with modifications as described in (Allaire et al., 2013, PMID: 23289891).
Scan protocol The processed GeneChip plate arrays were scanned using GeneTitan scanner (Affymetrix).
Description Gene expression data from ex vivo FACS-sorted T-cell subsets isolated from lacrimal gland and spleen cell suspensions
Data processing The data were analyzed with Partek Genomics Suite (Partek) using Affymetrix default analysis settings: RMA background correction, quantile normalization and median polish probeset summarization (log2).
 
Submission date Jun 08, 2016
Last update date Sep 01, 2016
Contact name MICHAEL MINGUENEAU
E-mail(s) [email protected]
Phone 8579199313
Organization name Biogen
Department Immunology
Street address 115 Broadway
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platform ID GPL11180
Series (1)
GSE83113 Gene expression analysis of total B, CD4+ T and epithelial cells in lacrimal glands from the NOD mouse model of Sjogren's syndrome

Data table header descriptions
ID_REF
VALUE Median Polish Probeset summarization (log2)

Data table
ID_REF VALUE
1415670_PM_at 7.22972
1415671_PM_at 8.3089
1415672_PM_at 8.18975
1415673_PM_at 7.08875
1415674_PM_a_at 7.61817
1415675_PM_at 8.80338
1415676_PM_a_at 10.1077
1415677_PM_at 7.33905
1415678_PM_at 10.5807
1415679_PM_at 10.3218
1415680_PM_at 8.42594
1415681_PM_at 7.5911
1415682_PM_at 7.22686
1415683_PM_at 9.00704
1415684_PM_at 6.63356
1415685_PM_at 7.01171
1415686_PM_at 9.32714
1415687_PM_a_at 9.40831
1415688_PM_at 9.29689
1415689_PM_s_at 6.39331

Total number of rows: 45141

Table truncated, full table size 983 Kbytes.




Supplementary file Size Download File type/resource
GSM2193170_080414_108_107.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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