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Sample GSM1861791 Query DataSets for GSM1861791
Status Public on Aug 27, 2015
Title allograft kidney 476
Sample type RNA
 
Source name Donor kidney from a BALB/c mouse latently infected with MCMV
Organism Mus musculus
Characteristics tissue: Allograft Kidney
age: 48 hours post transplant
strain: BALB/c
Treatment protocol Donor kidneys from latently infected BALB/c mice were transplanted into recipient C57BL/6 mice as previously described (Zhang et al., 1995), except that recipients were bi-laterally nephrectomized at the time of the transplant. The pararenal glands were left intact. The contralateral donor kidney was frozen in liquid nitrogen at the time of the transplant for use as a matching, Day 0 latent control. Transplanted kidneys were frozen in liquid nitrogen at the time of sacrifice.
Growth protocol BALB/c and C57BL/6 mice were purchased from The Jackson Laboratory (Bar Harbor, ME). MCMV (Smith strain) was purchased from the American Type Culture Collection (Manassas, VA), and propagated in mice by harvesting salivary glands 14 days post-infection. Virus stocks were titered on confluent monolayers of murine embryo fibroblasts. To establish latency, three to four-week old female BALB/c mice were infected i.p. with 5 x 105 pfu of MCMV (Smith strain) and housed for 3-6 months in the Northwestern University Center for Comparative Medicine.
Extracted molecule total RNA
Extraction protocol Frozen tissue collected at 48 hr post-transplant was immediately transferred to tubes containing TriZol and 5 mm stainless steel beads (Qiagen), and the tissue was disrupted by mechanical shaking in a TissueLyser (Qiagen) at room temperature for 5 min. RNAs were purified with PureLink RNA Minikits (Ambion), using on-column DNAse treatment as directed by the manufacturer. RNA was quantified on a nanodrop spectrophotometer, and quality was assessed on an Agilent 2100 bioanalyzer.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Affymetrix Mouse Gene 2.1 ST ArrayArray. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description transplanted kidney control replicate from mouse 476
Data processing The data were analyzed with Partek Genomics Suite 6.6 using Robubst Multiarray Average (RMA) algorithm with quantile normalization method.
 
Submission date Aug 26, 2015
Last update date Aug 27, 2015
Contact name Chunfa Jie
E-mail(s) cjie.jhmi@gmail.com
Phone 3124043831
Organization name Des Moines University
Street address 3200 Grand Ave
City Des Moines
State/province IA
ZIP/Postal code 50266
Country USA
 
Platform ID GPL17400
Series (1)
GSE72392 Kidney gene expression profile following the transplant-induced reactivation of MCMV

Data table header descriptions
ID_REF
VALUE Partek Genomics Suite 6.6 Robubst Multiarray Average (RMA) signal intensities

Data table
ID_REF VALUE
17200001 105.367052
17200003 125.3093278
17200005 108.7604338
17200007 78.55384564
17200009 69.68566473
17200011 72.3559624
17200013 24.64785166
17200015 80.21388037
17200017 34.66048651
17200019 26.65990991
17200021 40.33107625
17200023 187.9845129
17200025 63.1552166
17200027 81.32460472
17200029 62.25207409
17200031 52.9911672
17200033 46.84879384
17200035 21.24011983
17200037 44.78892082
17200039 49.35519357

Total number of rows: 41345

Table truncated, full table size 843 Kbytes.




Supplementary file Size Download File type/resource
GSM1861791_X476G1.CEL.gz 5.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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