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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
AG0151 Resource Report Resource Website Discontinued |
RRID:CVCL_8B51 | Homo sapiens (Human) | Alagille syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:90081517, Wikidata:Q54609444 |
CVCL_8B51 | 2026-08-01 05:57:37 | 0 | ||||||
|
AG01947 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_V553 | Homo sapiens (Human) | Sporadic retinoblastoma |
PMID:7253718 PMID:7471105 |
Finite cell line | Male | AG-1947, AG 1947, AG1947 | Coriell:AG01947, Wikidata:Q54609537 |
CVCL_V553 | 2026-08-01 05:57:36 | 0 | |||||
|
AG01964 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE21 | Homo sapiens (Human) | Cowden syndrome | PMID:7253718 | Finite cell line | Male | AG-1964, AG 1964, AG1964 | Coriell:AG01964, Wikidata:Q54609546 |
CVCL_JE21 | 2026-08-01 05:57:36 | 0 | |||||
|
AG01950 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01950, RRID:CVCL_JE29 | Homo sapiens (Human) | Xeroderma pigmentosum | Finite cell line | Male | AG-1950, AG 1950 | Coriell | AG01950 | Coriell:AG01950, Wikidata:Q54609539 |
CVCL_JE29 | 2026-08-01 05:57:37 | 0 | ||||
|
AG00780 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_U282 | Homo sapiens (Human) | Werner syndrome |
PMID:6223188 PMID:7176709 PMID:7253718 PMID:24749076 PMID:26984941 |
Finite cell line | Male | AG 780, AG780, AG00780F, GM00780, GM-780, GM 780, GM780 | CLO:CLO_0036916, Coriell:AG00780, Coriell:GM00780, GEO:GSM1184264, GEO:GSM1184265, GEO:GSM1535458, GEO:GSM1535467, Wikidata:Q54609418 |
CVCL_U282 | 2026-08-01 05:57:35 | 0 | |||||
|
AG01440 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01440, RRID:CVCL_2Q69 | Homo sapiens (Human) | Population: African American. | PMID:7253718 | Finite cell line | Male | AG-1440, AG 1440, AG1440 | Coriell | AG01440 | CLO:CLO_0036893, Coriell:AG01440, Wikidata:Q54609439 |
CVCL_2Q69 | 2026-08-01 05:57:35 | 0 | |||
|
AG01231 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2KR | Homo sapiens (Human) | Sporadic retinoblastoma | PMID:7253718 | Finite cell line | Female | AG1231 | Coriell:AG01231, Wikidata:Q105506059 |
CVCL_A2KR | 2026-08-01 05:57:35 | 0 | |||||
|
AG01232 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01232, RRID:CVCL_A2PF | Homo sapiens (Human) | Sporadic retinoblastoma | PMID:7253718 | Finite cell line | Female | AG1232 | Coriell | AG01232 | Coriell:AG01232, Wikidata:Q105506063 |
CVCL_A2PF | 2026-08-01 05:57:35 | 0 | |||
|
AG0124 Resource Report Resource Website Discontinued |
RRID:CVCL_8B47 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:90052207, Wikidata:Q54609426 |
CVCL_8B47 | 2026-08-01 05:57:36 | 0 | ||||||
|
AG00781 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG00781, RRID:CVCL_W842 | Homo sapiens (Human) | Progeria | Finite cell line | AG0781B | Coriell | AG00781 | Coriell:AG00781, Wikidata:Q54609419 |
CVCL_W842 | 2026-08-01 05:57:35 | 0 | |||||
|
AG0152 Resource Report Resource Website Discontinued |
RRID:CVCL_8B52 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:90082301, Wikidata:Q54609452 |
CVCL_8B52 | 2026-08-01 05:57:36 | 0 | ||||||
|
AG01946 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_V552 | Homo sapiens (Human) | Sporadic retinoblastoma | PMID:7471105 | Finite cell line | Male | AG-1946, AG 1946, AG1946 | Coriell:AG01946, Wikidata:Q54609534 |
CVCL_V552 | 2026-08-01 05:57:36 | 0 | |||||
|
AG01894 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE45 | Homo sapiens (Human) | Kidney Wilms tumor | Donor information: Established from the irradiated skin of a Wilm's tumor patient. | PMID:7253718 | Finite cell line | Male | AG-1894, AG 1894, AG1894 | Coriell:AG01894, Wikidata:Q54609530 |
CVCL_JE45 | 2026-08-01 05:57:36 | 0 | ||||
|
AG01965 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE22 | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Female | AG-1965, AG 1965, AG1965 | Coriell:AG01965, Wikidata:Q54609548 |
CVCL_JE22 | 2026-08-01 05:57:37 | 0 | ||||||
|
AG0143 Resource Report Resource Website Discontinued |
ECACC Cat# 90072402, RRID:CVCL_8B49 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90072402 | ECACC:90072402, Wikidata:Q54609433 |
CVCL_8B49 | 2026-08-01 05:57:35 | 0 | ||||
|
AG01946 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01946, RRID:CVCL_V552 | Homo sapiens (Human) | Sporadic retinoblastoma | PMID:7471105 | Finite cell line | Male | AG-1946, AG 1946, AG1946 | Coriell | AG01946 | Coriell:AG01946, Wikidata:Q54609534 |
CVCL_V552 | 2026-08-01 05:57:38 | 0 | |||
|
AG01615 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_V541 | Homo sapiens (Human) | Kidney Wilms tumor | Donor information: Established from the non-irradiated skin of a nephroblastoma patient. |
PMID:7253718 PMID:7471105 |
Finite cell line | Male | AG-1615, AG 1615, AG1615 | Coriell:AG01615, Wikidata:Q54609463 |
CVCL_V541 | 2026-08-01 05:57:37 | 0 | ||||
|
AG0179 Resource Report Resource Website Discontinued |
ECACC Cat# 90101202, RRID:CVCL_8B54 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90101202 | ECACC:90101202, Wikidata:Q54609528 |
CVCL_8B54 | 2026-08-01 05:57:36 | 0 | ||||
|
AG01895 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01895, RRID:CVCL_JE46 | Homo sapiens (Human) | Kidney Wilms tumor | Donor information: Established from the non-irradiated skin of a Wilm's tumor patient. | PMID:7253718 | Finite cell line | Male | AG-1895, AG 1895, AG1895 | Coriell | AG01895 | Coriell:AG01895, Wikidata:Q54609533 |
CVCL_JE46 | 2026-08-01 05:57:36 | 0 | ||
|
AG01485 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE37 | Homo sapiens (Human) | Population: African American. | PMID:7253718 | Finite cell line | Male | AG-1485, AG 1485, AG1485 | Coriell:AG01485, Wikidata:Q54609441 |
CVCL_JE37 | 2026-08-01 05:57:35 | 0 |
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