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Sample GSM1861789 Query DataSets for GSM1861789
Status Public on Aug 27, 2015
Title allograft kidney 475
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 475
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) [email protected]
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 129.8516018
17200003 140.6572396
17200005 117.2252869
17200007 32.84336404
17200009 94.80360402
17200011 54.54745569
17200013 33.17167598
17200015 50.18798085
17200017 31.59183866
17200019 36.36553762
17200021 48.27117367
17200023 160.047907
17200025 110.9526258
17200027 60.52209404
17200029 65.87960501
17200031 37.09364151
17200033 34.271561
17200035 7.966742803
17200037 25.93143249
17200039 42.39317163

Total number of rows: 41345

Table truncated, full table size 843 Kbytes.




Supplementary file Size Download File type/resource
GSM1861789_X475G1.CEL.gz 4.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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