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Sample GSM8381324 Query DataSets for GSM8381324
Status Public on Jul 20, 2024
Title wild type embryo-1
Sample type RNA
 
Source name 12 days embryo
Organism Mus musculus
Characteristics tissue: embryo
strain: C57BL/6J
Growth protocol The animal housing facility is a barrier housing facility, and it is maintained in accordance with the national standards (Laboratory Animal-Requirements of Environment and Housing Facilities, GB 14925–2001).
Extracted molecule total RNA
Extraction protocol Total RNA of tumor tissue were isolated using Trizol. RNA quantity and quality were measured by NanoDrop ND-1000. RNA integrity was assessed by standard denaturing agarose gel electrophoresis.
Label Cy3
Label protocol total RNA from each sample was linearly amplified and labeled with Cy3-UTP.The Labeled cRNAs were purified by RNeasy Mini Kit (Qiagen). The concentration and specific activity of the labeled cRNAs (pmol Cy3/μg cRNA) were measured by NanoDrop ND-1000.
 
Hybridization protocol 1 μg of each labeled cRNA was fragmented by adding 11 μl 10 × Blocking Agent and 2.2 μl of 25×Fragmentation Buffer, then heated at 60°C for 30 min, and finally 55 μl 2 × GE Hybridization buffer was added to dilute the labeled cRNA. 100 μl of hybridization solution was dispensed into the gasket slide and assembled to the gene expression microarray slide. The slides were incubated for 17 hours at 65°C in an Agilent Hybridization Oven.
Scan protocol The hybridized arrays were washed, fixed and scanned with using the Agilent DNA Microarray Scanner (part number G2505C).
Data processing Agilent Feature Extraction software (version 11.0.1.1) was used to analyze acquired array images.
 
Submission date Jul 07, 2024
Last update date Jul 20, 2024
Contact name LI XU
E-mail(s) xulihhb@gmail.com
Phone 13003691133
Organization name Zhejiang Chinese Medical University
Department School of Basic Medical Science
Street address Binwen 7-3-1101,Binwen Road
City HangZhou
State/province Zhejiang Province
ZIP/Postal code 310053
Country China
 
Platform ID GPL11202
Series (1)
GSE271656 Transcriptome analysis of embryos of STAT3-K177R/K180R mutant mice

Data table header descriptions
ID_REF
VALUE Quantile normalization and subsequent data processing were performed with using the GeneSpring GX v12.1 software package (Agilent Technologies). After quantile normalization of the raw data, genes that at least 6 out of 9 samples have flags in Detected (“All Targets Value”) were chosen for further data analysis. Differentially expressed genes with statistical significance between the two groups were identified through Volcano Plot filtering. Differentially expressed genes between the two samples were identified through Fold Change filtering. Hierarchical Clustering was performed using the R scripts. GO analysis and Pathway analysis were performed in the standard enrichment computation method.

Data table
ID_REF VALUE
A_55_P1989846 8.288954
A_55_P1991598 3.920407
A_55_P2022211 10.877071
A_55_P1980764 5.460216
A_55_P1964375 10.198497
A_51_P128876 10.738929
A_51_P207591 8.191884
A_55_P2131920 11.890318
A_55_P2404223 5.710818
A_55_P2101944 14.85902
A_52_P358860 7.6826997
A_51_P119031 10.633626
A_51_P309854 7.304757
A_51_P343900 11.906054
A_51_P234359 8.535982
A_51_P487813 11.96619
A_52_P613977 9.764423
A_55_P1957209 4.5146894
A_52_P549166 8.273166
A_55_P2052210 13.993869

Total number of rows: 30478

Table truncated, full table size 687 Kbytes.




Supplementary file Size Download File type/resource
GSM8381324_b4.txt.gz 2.1 Mb (ftp)(http) TXT

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