Hs 229.THomo sapiens (Human)Undefined cell line type
Also known as: HS229T, Hs229T, Hs-229-T
🤖 AI SummaryBased on 2 publications
Quick Overview
Human lung fibroblast cell line for cancer research
Detailed Summary
Hs 229.T is a human lung fibroblast cell line derived from a tumor tissue. It is commonly used in cancer research due to its fibroblast characteristics. The cell line provides a valuable model for studying lung-related diseases and cancer mechanisms. Its use in research applications is supported by its availability in major cell line databases and its utility in various experimental models.
Research Applications
Cancer researchLung disease studies
Key Characteristics
Human originFibroblast morphologyLung tissue derivation
Generated on 6/15/2025
Basic Information
Database ID | CVCL_0698 |
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Species | Homo sapiens (Human) |
Tissue Source | Lung[UBERON:UBERON_0002048] |
Donor Information
Age | 65 |
---|---|
Age Category | Adult |
Sex | Male |
Race | caucasian |
Disease Information
Disease | Non-Cancerous |
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Lineage | Fibroblast |
Subtype | Fibroblast, Soft Tissue |
DepMap Information
Source Type | ATCC |
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Source ID | ACH-000131_source |
Haplotype Information (STR Profile)
Short Tandem Repeat (STR) profile for cell line authentication.
Amelogenin
X,Y
CSF1PO
10,11
D13S317
12,13
D16S539
14
D5S818
11
D7S820
9,10
TH01
9
TPOX
8
vWA
15,16
Gene Expression Profile
Gene expression levels and statistical distribution
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Full DepMap dataset with combined data across cell lines
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Publications
Next-generation characterization of the Cancer Cell Line Encyclopedia.
Sellers W.R.
Nature 569:503-508(2019).
An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.
Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.
Cancer Res. 79:1263-1273(2019).
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.
Nature 483:603-607(2012).
Fibroblasts cell lines misclassified as cancer cell lines.";
de Weck A., Bitter H., Kauffmann A.
bioRxiv 2017:166199-166199(2017).