NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM835204 Query DataSets for GSM835204
Status Public on Jan 01, 2022
Title Lmajor_WT_rep2
Sample type RNA
 
Source name Leishmania major infected wild-type mice replicate2
Organism Mus musculus
Characteristics strain: Balb/c
Sex: male
tissue: bone marrow cells
genotype/variation: wild type
Treatment protocol Mice were subcutaneously inoculated with Leishmania major promastigotes at right hind foot pad for 4 weeks.
Extracted molecule total RNA
Extraction protocol RNA was prepared using the miRNeasy Kit (Qiagen, 217004) following the manufacturer's recommendations. The protocol includes on-column DNase digestion. RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared using Low Input Quick Amp Labeling Kit, One-Color (Agilent, 5190-2305) according to manufacturer's instructions (One-Color Microarray-Based Gene Expression Analysis Low Input Quick Amp Labeling, v6.5, May 2010), followed by RNAeasy column purification (Qiagen, 4106).
 
Hybridization protocol Hybridization and washing were done using Agilent Gene Expression Hybridization Kit (Agilent, 5188-5242) and Agilent Wash Buffer Kit (Agilent, 5188-5327) according to manufacturer's protocols (One-Color Microarray-Based Gene Expression Analysis Low Input Quick Amp Labeling, v6.5 May 2010).
Scan protocol Slides were scanned after washing on the Agilent Microarray Scanner (G2565CA) using one color scan setting for 4x44k array slides (Profile: AgilentHD_GX1col, Resolution: 5 μm).
Description Mac1+ cells were sorted from bone marrow cells and analyzed.
Data processing The scanned images were analyzed with Feature Extraction Software using default parameters to obtain background subtracted and spatially detrended Processed Signal intensities. Further data processing was done using GeneSpring GX Software v11.0.
 
Submission date Nov 17, 2011
Last update date Jan 01, 2022
Contact name Yoko Fukuda Yuzawa
Organization name Max-Planck Institute of Immunobiology
Street address Stübeweg 51
City Freiburg
ZIP/Postal code 79108
Country Germany
 
Platform ID GPL7202
Series (1)
GSE33765 Leishmania major infected WT and miR-223 KO mice

Data table header descriptions
ID_REF
VALUE Signal intensity was normalized by median using Gene Spring GX Software v11.0. Values are in log scale.

Data table
ID_REF VALUE
A_51_P100021 3.5906348
A_51_P100034 11.850609
A_51_P100052 2.459921
A_51_P100063 4.2572675
A_51_P100084 5.779253
A_51_P100099 8.51605
A_51_P100155 10.52565
A_51_P100174 10.785669
A_51_P100181 8.222225
A_51_P100218 0.9286312
A_51_P100227 9.394375
A_51_P100238 1.1858028
A_51_P100246 10.126223
A_51_P100289 11.301147
A_51_P100298 8.258144
A_51_P100309 1.5080217
A_51_P100327 10.482376
A_51_P100347 4.901185
A_51_P100379 3.7393444
A_51_P100428 1.7321976

Total number of rows: 41250

Table truncated, full table size 910 Kbytes.




Supplementary file Size Download File type/resource
GSM835204_US91803681_251486829928_S01_GE1_105_Dec08_1_4.txt.gz 9.1 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap