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Sample GSM864796 Query DataSets for GSM864796
Status Public on Mar 31, 2013
Title Tg ligament tissue
Sample type RNA
Source name ligament tissue from transgenic mice
Organism Mus musculus
Characteristics background strain: C57BL/6J
genotype: A transgenic
tissue: ligament
Growth protocol Mesenchymal stem cells (sample 1) derived from mouse embryos were obtained from the Cell Bank RIKEN Bioresource Center, Japan. The cells were suspended in E-MEM and Dulbecco’s Modified Eagle’s medium containing 10% foetal bovine serum (FBS) to a final concentration of 1.5 × 10^5 cells/ml, were seeded into dishes or flasks (2.0 × 10^4 cells/cm2), and were statically cultured at 37°C under 5% CO2. For the expression of murine proteins, the synthesized mouse A sequence was inserted into XhoI of the pCAGGS vector, which was then cloned and transfected into mouse mesenchymal stem cells. Protein expression in the culture supernatant was confirmed by Western blotting (sample 4). The plasmid DNA pCAGGS-XhoI-A-XhoI was used for introduction of the gene into 58 fertilized mouse eggs. These were then implanted into surrogate mouse mothers. A section of tail tissue was cut from 20 of the resulting newborn mice, and DNA was extracted using the DNA mini kit (QIAGEN). PCR was performed to determine whether the samples contained the exogenous gene. Comparison of microarray analyses with mesenchymal stem cells showed homology between the extracellular matrix of the ligament tissues of Wt mice (sample 3), the ligament tissues of mice transgenic for A (sample 2), and mesenchymal stem cell-derived ligament-like tissue.
Extracted molecule total RNA
Extraction protocol Total RNA was prepared from cells using an AllPrep DNA/RNA Mini Kit (Qiagen) according to the manufacturer’s instructions.
Label Cy3
Label protocol cRNA was amplified and labelled using a Quick Amp Labelling Kit (Agilent Technologies).
Hybridization protocol cRNA was hybridized to a 44K 60-mer oligomicroarray (Whole Mouse Genome Microarray Kit; Agilent Technologies) according to the manufacturer's instructions.
Scan protocol The hybridized microarray slides were scanned using an Agilent scanner. The relative hybridization intensities and background hybridization values were calculated using Feature Extraction Software version (Agilent Technologies).
Description Sample 2
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent) using default parameters to obtain background subtracted and spatially detrended Processed Signal intensities. The raw signal intensities and flags for each probe were calculated from the hybridization intensities and spot information according to the procedures recommended by Agilent Technologies using the Flag criteria in the GeneSpring Software. In addition, the raw signal intensities of two samples were normalized by the quantile algorithm with Bioconductor.
Submission date Jan 23, 2012
Last update date Mar 31, 2013
Contact name Michiyo Tsuru
Phone 81-942-31-7568
Organization name Kurume Universuty
Department Orthopardic Surgery
Street address 67 Asahimachi
City Kurume
State/province Fukuoka
ZIP/Postal code 830-0011
Country Japan
Platform ID GPL11202
Series (1)
GSE35269 New protein from an unexpected ligament

Data table header descriptions
VALUE Quantile-normalized signal (non-log scaled)

Data table
A_55_P2116608 62.984085 P
A_55_P2073489 407.98155 P
A_52_P229709 3871.1605 P
A_55_P2092526 1074.3838 P
A_55_P2048358 6.38587575 A
A_55_P2109122 21144.165 P
A_55_P2032147 1240.549875 P
A_55_P1985351 12.72499425 A
A_55_P2145838 114.8084525 P
A_51_P163444 1552.758424 P
A_55_P2166688 4569.7965 P
A_55_P2230663 11.5031975 A
A_55_P2195172 7.04313925 A
A_55_P1953663 5.6973165 A
A_55_P2135730 6.4117915 A
A_51_P174143 71.3732925 P
A_51_P419971 5236.8055 P
A_55_P1967880 3967.63975 P
A_55_P2364315 114.1619475 P
A_51_P154780 9.93541125 A

Total number of rows: 39429

Table truncated, full table size 1007 Kbytes.

Supplementary file Size Download File type/resource
GSM864796.txt.gz 9.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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