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Status |
Public on Jan 01, 2024 |
Title |
lo-GelMA |
Sample type |
SRA |
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Source name |
skin wound+hydrogel
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Organism |
Mus musculus |
Characteristics |
tissue: skin wound+hydrogel genotype: c57bl/6 treatment: lo-GelMA
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Extracted molecule |
total RNA |
Extraction protocol |
PWD5 wound tissue was dissected from the surrounding edge and healthy tissue, minced with scissors, and then dissociated with 10 ml solution of 2.7 mg/mL collagenase P (Sigma), 1mM pyruvate, 10 mM HEPES, in RPMI basal media at 37°C for 2 hours at 37C, triturating every 15 minutes. Digestion was halted with the addition of 2ml 2% FBS and live cells were isolated using Miltenyi dead cell separation kit and MS columns, per manufacturer’s instructions. Cells were finally suspended in 1ml 0.04% BSA and kept on ice until processed for library preparation. RNA library was prepared using a 10X Chromium V3.1 kit and sequenced with NovaSeq on an S4 flow cell (UCI Genomic High Throughput Facility).
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Library strategy |
RNA-Seq |
Library source |
transcriptomic single cell |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
10X Chromium sequencing FASTQ output files were aligned using Cell Ranger Assembly: mm10 Supplementary files format and content: tab separated values and matrix
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Submission date |
Nov 23, 2023 |
Last update date |
Jan 01, 2024 |
Contact name |
Sergei Butenko |
Organization name |
University of California, Irvine
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Street address |
Irvine
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City |
Irvine |
State/province |
CA |
ZIP/Postal code |
92617 |
Country |
USA |
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Platform ID |
GPL24247 |
Series (1) |
GSE248524 |
Hydrogel crosslinking modulates macrophages, fibroblasts, and their communication, during wound healing |
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Relations |
BioSample |
SAMN38391795 |
SRA |
SRX22629193 |
Supplementary file |
Size |
Download |
File type/resource |
GSM7916354_2_combined_files.tar.gz |
116.9 Mb |
(ftp)(http) |
TAR |
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