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Series GSE215840 Query DataSets for GSE215840
Status Public on Oct 01, 2023
Title In-Depth Characterization of Cell Subculture Process based on Multi-Omics
Organism Chlorocebus aethiops
Experiment type Expression profiling by high throughput sequencing
Summary To investegate the mechanism of physiological changes during cell digestion, we analyzed the levels of RNAs in cells treated with animal-based enzymes and animal origin-free enzymes.
 
Overall design The Vero cells were divided into 3 groups. The first group (Group 1) was digested with trypsin at 37°C. The cells collected immediately after digestion were set to 0 h, and the digested cells were placed back in the cell incubator for 8 hours. After the cells were digested with non-enzymatic digestion solution and then collected for 8 h, the cells af-ter trypsinization at 37°C were further cultured for 24 hours, and the cells were di-gested with non-enzymatic digestion solution and collected for 24 h. The second group (Group 2) was digested with TrypLE at 37°C, then set the cells collected immediately after digestion as 0 h, place the digested cells back in the cell incubator for 8 hours, and digest the recovered cells with non-enzyme digestion solution. Set it to 8h, continue to culture the cells digested with TrypLE digestion solution at 37°C for 24 hours, and then digest the cells with non-enzyme digestion solution for 24h. The third group (Group 3) used 4°C TrypLE digestion solution at 25°C digestion, the cells collected immediately after digestion were set to 0 h, and the digested cells were placed back in the cell incu-bator for 8 hours, and the cells collected after digestion with non-enzyme digestion solution were set to 8 h, and digested with TrypLE digestion solution at 4°C. After the cells were cultured for 24 hours, the collected cells were digested with non-enzymatic digestion solution and set to 24 hours. In addition, Vero cells were digested with an enzyme-free digestion solution at 37°C, and the immediately harvested cells were set as the control group. Each sample has three biological replicates.
 
Contributor(s) Yu S, Huang Y, Wu C, Fu W, Liang H, Chen C, Cheng Y, Guo Y, Zhang Y, Wang H, Yang X
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Oct 15, 2022
Last update date Oct 01, 2023
Contact name Yunchao Huang
E-mail(s) ychaohuang@bjmu.edu.cn
Organization name Beijing Institute of Biological Products Company Limited
Street address Boxing 2nd Road
City Beijing
ZIP/Postal code 100176
Country China
 
Platforms (1)
GPL29682 Illumina NovaSeq 6000 (Chlorocebus aethiops)
Samples (30)
GSM6643095 Vero cells, CTR, rep1
GSM6643096 Vero cells, CTR, rep2
GSM6643097 Vero cells, CTR, rep3
Relations
BioProject PRJNA890891

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE215840_G1_0hvsG2_0h_all_KEGGenrich.xls.gz 23.2 Kb (ftp)(http) XLS
GSE215840_G1_0hvsG2_0h_all_KEGGenrich_significant.xls.gz 2.5 Kb (ftp)(http) XLS
GSE215840_G1_0hvsG2_0h_deg_all.xls.gz 236.5 Kb (ftp)(http) XLS
GSE215840_Union_for_cluster.xls.gz 23.3 Kb (ftp)(http) XLS
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Raw data are available in SRA
Processed data are available on Series record

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