NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2647787 Query DataSets for GSM2647787
Status Public on Dec 25, 2018
Title AJ control d0 #2, batch A
Sample type RNA
 
Source name Control femur bone
Organism Mus musculus
Characteristics tissue: bone
gender: male
batch: batch A
strain: AJ
diet: control
timepoint: day 0
animal: 1002
Treatment protocol Pi group: Phosphate deficiency (Pi) was initiated 2 days prior to fracture and was maintained for 15 days by supplying the mice with a low phosphate diet (Harlan Laboratories, Madison, WI). Phosphate was then replenished and bone healing was allowed to continue until 35 days. For the three strains of mice, control groups were included where the mice were given normal diet throughout the study.
Growth protocol In vivo animal model
Extracted molecule total RNA
Extraction protocol Total RNAs were isolated from each fracture callus using procedures developed for murine bones (Wang et al., Matrix Biology, 2006; 25(5):271-81). In order to both achieve an optimal balance in biological replicate variability and repeatability RNA from every two of the six fracture calluses were randomly pooled to generate three assay samples.
Label biotin
Label protocol Biotin labeling was performed using the Ambion WT Expression Kit (Life Technologies, Grand Island, NY) according to the manufacturer's protocol, followed by the GeneChip WT Terminal Labeling and Controls Kit (Affymetrix, Santa Clara, CA).
 
Hybridization protocol The labeled, fragmented DNA was hybridized to the Affymetrix Mouse Gene 1.0 ST Array for 18 hours in a GeneChip Hybridization oven 640 at 45oC with rotation (60 rpm). The hybridized samples were washed and stained using an Affymetrix fluidics station 450.
Scan protocol After staining, microarrays were immediately scanned using an Affymetrix GeneArray Scanner 3000 7G Plus.
Description Gene expression data from right femur of AJ control animal at baseline.
Data processing Raw Affymetrix CEL files were normalized to produce Entrez Gene-identifier-specific expression values using the implementation of the Robust Multiarray Average (RMA) in the affy Bioconductor package (version 1.36.1), using R version 2.15.1 and the Brainarray mogene10stmmentrezg R package (version 16.0.0).
 
Submission date Jun 01, 2017
Last update date Jun 25, 2019
Contact name Boston University Microarray and Sequencing Resource
E-mail(s) msrdata@bu.edu
Organization name Boston University
Department Microarray and Sequencing Resource
Street address 72 East Concord Street, E631
City Boston
State/province MA
ZIP/Postal code 02118
Country USA
 
Platform ID GPL19485
Series (1)
GSE99580 A Systems Genetics Approach to Fracture Healing

Data table header descriptions
ID_REF
VALUE log2-transformed, RMA-normalized Entrez Gene expression values

Data table
ID_REF VALUE
100008567_at 5.7586708
100009600_at 4.833935678
100009609_at 2.691862204
100009614_at 4.841794839
100012_at 3.654986806
100017_at 8.690023225
100019_at 7.160632895
100033459_at 4.101388903
100034251_at 5.645065765
100034748_at 5.274088533
100036520_at 5.140548939
100036521_at 6.481064255
100036523_at 6.262144902
100036537_at 4.689902778
100036768_at 4.501980481
100037258_at 9.046354504
100037260_at 5.603107201
100037262_at 6.313662973
100037278_at 8.966291948
100037396_at 4.977426214

Total number of rows: 21187

Table truncated, full table size 442 Kbytes.




Supplementary file Size Download File type/resource
GSM2647787_2014-06-17_LG_A1_1002.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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