Searching the RRID Resource Information Network
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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.
| Name | Proper Citation | Organism | Disease |
Comments |
Defining Citation | Category | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
TPA2-14 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_XA85 | Mus musculus (Mouse) | Group: Patented cell line. | PMID:1713912 | Hybridoma | TPA 2-14 | CCRID:4201PAT-CCTCC00063, JCRB:IFO50194, Wikidata:Q98133517 |
cvcl_3412 | CVCL_XA85 | 2026-08-15 05:00:06 | 0 | |||||
|
TS 9-7 Resource Report Resource Website Discontinued |
RRID:CVCL_V444 | Homo sapiens (Human) | Autosomal dominant polycystic kidney disease | PMID:12734101 | Transformed cell line | Female | ATCC:CRL-2831, BioSample:SAMN03471800, Wikidata:Q54973049 |
CVCL_V444 | 2026-08-15 05:00:11 | 0 | ||||||
|
TS-ED Resource Report Resource Website Discontinued |
RRID:CVCL_Y122 | Homo sapiens (Human) | Ehlers-Danlos syndrome, type IV | Finite cell line | Female | ATCC:CRL-1406, Wikidata:Q54973054 |
CVCL_Y122 | 2026-08-15 05:00:11 | 0 | |||||||
|
TS-ED Resource Report Resource Website Discontinued |
ATCC Cat# CRL-1406, RRID:CVCL_Y122 | Homo sapiens (Human) | Ehlers-Danlos syndrome, type IV | Finite cell line | Female | ATCC | CRL-1406 | ATCC:CRL-1406, Wikidata:Q54973054 |
CVCL_Y122 | 2026-08-15 05:00:16 | 0 | |||||
|
TS 10-7 Resource Report Resource Website Discontinued |
ATCC Cat# CRL-2835, RRID:CVCL_V442 | Homo sapiens (Human) | Autosomal dominant polycystic kidney disease | PMID:12734101 | Transformed cell line | Female | ATCC | CRL-2835 | ATCC:CRL-2835, Wikidata:Q54973046 |
CVCL_V442 | 2026-08-15 05:00:11 | 0 | ||||
|
TSGH-8301 Resource Report Resource Website Contaminated Discontinued |
RRID:CVCL_A342 | Homo sapiens (Human) | Human papillomavirus-related cervical squamous cell carcinoma | Miscellaneous: STR profile from personal communication of Chow, Kin-Hoe., Population: Caucasian., Problematic cell line: Contaminated. Shown to be a ME-180 derivative (BCRC=60145 and STR profile). Originally thought to originate from a 56 year old male patient with a grade 2 stage A papillary transitional cell carcinoma.. |
PMID:3352272 PMID:29732388 |
Cancer cell line | Female | TSGH8301, TSGH 8301, Tri-Service General Hospital-8301 | BCRC:60145, cancercelllines:CVCL_A342, Cosmic:755397, Wikidata:Q54973126 |
cvcl_1401 | CVCL_A342 | 2026-08-15 05:00:13 | 0 | |||
|
TT0113 Resource Report Resource Website Discontinued |
ECACC Cat# 90062723, RRID:CVCL_8Y80 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90062723 | ECACC:90062723, Wikidata:Q54973187 |
CVCL_8Y80 | 2026-08-15 05:00:19 | 0 | |||||
|
TT0122 Resource Report Resource Website Discontinued |
RRID:CVCL_8Y83 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:90081619, Wikidata:Q54973195 |
CVCL_8Y83 | 2026-08-15 05:00:14 | 0 | ||||||
|
TT0153 Resource Report Resource Website Discontinued |
RRID:CVCL_8Y87 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:91012413, Wikidata:Q54973199 |
CVCL_8Y87 | 2026-08-15 05:00:15 | 0 | ||||||
|
TT2 Resource Report Resource Website 1+ mentions Discontinued |
RCB Cat# AES0014, RRID:CVCL_C318 | Mus musculus (Mouse) | Part of: ENCODE project mouse cell lines. |
PMID:8250257 PMID:9353641 |
Embryonic stem cell | Male | TT2 ES, ES-TT2 | RCB | AES0014 | BTO:BTO_0004639, EFO:EFO_0005485, ENCODE:ENCBS317ENC, ENCODE:ENCBS472MMU, GEO:GSM450274, GEO:GSM450284, RCB:AES0014, RCB:RCB2077, SKIP:SKIP001624, Wikidata:Q54973221 |
CVCL_C318 | 2026-08-15 05:00:19 | 5 | |||
|
TT0115 Resource Report Resource Website Discontinued |
RRID:CVCL_8Y82 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:90062725, Wikidata:Q54973189 |
CVCL_8Y82 | 2026-08-15 05:00:19 | 0 | ||||||
|
TT0151 Resource Report Resource Website Discontinued |
RRID:CVCL_8Y86 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:91012411, Wikidata:Q54973198 |
CVCL_8Y86 | 2026-08-15 05:00:14 | 0 | ||||||
|
TT0114 Resource Report Resource Website Discontinued |
ECACC Cat# 90062724, RRID:CVCL_8Y81 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90062724 | ECACC:90062724, Wikidata:Q54973188 |
CVCL_8Y81 | 2026-08-15 05:00:14 | 0 | ||||
|
TT0208 Resource Report Resource Website Discontinued |
ECACC Cat# 91042501, RRID:CVCL_8Y94 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91042501 | ECACC:91042501, Wikidata:Q54973209 |
CVCL_8Y94 | 2026-08-15 05:00:15 | 0 | |||||
|
TT0148 Resource Report Resource Website Discontinued |
ECACC Cat# 91012408, RRID:CVCL_8Y84 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012408 | ECACC:91012408, Wikidata:Q54973196 |
CVCL_8Y84 | 2026-08-15 05:00:14 | 0 | ||||
|
TT0154 Resource Report Resource Website Discontinued |
ECACC Cat# 91012414, RRID:CVCL_8Y88 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012414 | ECACC:91012414, Wikidata:Q54973201 |
CVCL_8Y88 | 2026-08-15 05:00:15 | 0 | ||||
|
TT0151 Resource Report Resource Website Discontinued |
ECACC Cat# 91012411, RRID:CVCL_8Y86 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012411 | ECACC:91012411, Wikidata:Q54973198 |
CVCL_8Y86 | 2026-08-15 05:00:19 | 0 | ||||
|
TT0211 Resource Report Resource Website Discontinued |
RRID:CVCL_8Y97 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:91042504, Wikidata:Q54973212 |
CVCL_8Y97 | 2026-08-15 05:00:19 | 0 | |||||||
|
TT0111 Resource Report Resource Website Discontinued |
RRID:CVCL_8Y78 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:90062721, Wikidata:Q54973183 |
CVCL_8Y78 | 2026-08-15 05:00:14 | 0 | |||||||
|
TSU-Pr1-B1 Resource Report Resource Website Contaminated |
RRID:CVCL_M904 | Homo sapiens (Human) | Bladder carcinoma | Population: Caucasian; Swedish., Problematic cell line: Contaminated. Parent cell line (TSU-Pr1) has been shown to be a T24 derivative.. | PMID:16086232 | Cancer cell line | Female | cancercelllines:CVCL_M904, Wikidata:Q54973171 |
cvcl_4014 | CVCL_M904 | 2026-08-15 05:00:14 | 0 |
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