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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
AG01437 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01437, RRID:CVCL_U701 | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Male | AG-1437, AG 1437, AG1437, AG01437B, HG3004 | Coriell | AG01437 | CLO:CLO_0036897, BioSamples:SAME56937, Coriell:AG01437, Wikidata:Q54609436 |
CVCL_U701 | 2026-08-01 05:57:37 | 0 | ||||
|
AG0138 Resource Report Resource Website Discontinued |
RRID:CVCL_8B48 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:90070301, Wikidata:Q54609432 |
CVCL_8B48 | 2026-08-01 05:57:35 | 0 | ||||||
|
AG0158 Resource Report Resource Website Discontinued |
RRID:CVCL_8B53 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:90091901, Wikidata:Q54609461 |
CVCL_8B53 | 2026-08-01 05:57:36 | 0 | ||||||
|
AG00991 Resource Report Resource Website Possibly Discontinued Possibly Discontinued |
RRID:CVCL_V551 | Homo sapiens (Human) | Progeria |
PMID:4412878 PMID:7253718 PMID:7471105 |
Finite cell line | Male | AG-991, AG 991, AG991, AG0991A, GM00991, GM-991, GM 991, GM991, L.D. | Coriell:AG00991, Coriell:GM00991, Wikidata:Q54609424 |
CVCL_V551 | 2026-08-01 05:57:36 | 0 | |||||
|
AG01756 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01756, RRID:CVCL_JE20 | Homo sapiens (Human) | Oculocerebrorenal syndrome | PMID:7253718 | Finite cell line | Male | AG-1756, AG 1756, AG1756 | Coriell | AG01756 | Coriell:AG01756, Wikidata:Q54609526 |
CVCL_JE20 | 2026-08-01 05:57:36 | 0 | |||
|
AG01616 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE42 | Homo sapiens (Human) | Kidney Wilms tumor | Donor information: Established from the irradiated skin of a nephroblastoma patient. | PMID:7253718 | Finite cell line | Male | AG-1616, AG 1616, AG1616 | Coriell:AG01616, Wikidata:Q54609464 |
CVCL_JE42 | 2026-08-01 05:57:36 | 0 | ||||
|
AG01964 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01964, RRID:CVCL_JE21 | Homo sapiens (Human) | Cowden syndrome | PMID:7253718 | Finite cell line | Male | AG-1964, AG 1964, AG1964 | Coriell | AG01964 | Coriell:AG01964, Wikidata:Q54609546 |
CVCL_JE21 | 2026-08-01 05:57:38 | 0 | |||
|
AG01710 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE27 | Homo sapiens (Human) | Progeria | PMID:7253718 | Finite cell line | Male | AG-1710, AG 1710, AG1710 | Coriell:AG01710, Wikidata:Q54609465 |
CVCL_JE27 | 2026-08-01 05:57:36 | 0 | |||||
|
AG0151 Resource Report Resource Website Discontinued |
ECACC Cat# 90081517, RRID:CVCL_8B51 | Homo sapiens (Human) | Alagille syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90081517 | ECACC:90081517, Wikidata:Q54609444 |
CVCL_8B51 | 2026-08-01 05:57:36 | 0 | ||||
|
AG01485 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01485, RRID:CVCL_JE37 | Homo sapiens (Human) | Population: African American. | PMID:7253718 | Finite cell line | Male | AG-1485, AG 1485, AG1485 | Coriell | AG01485 | Coriell:AG01485, Wikidata:Q54609441 |
CVCL_JE37 | 2026-08-01 05:57:37 | 0 | |||
|
AG0152 Resource Report Resource Website Discontinued |
ECACC Cat# 90082301, RRID:CVCL_8B52 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90082301 | ECACC:90082301, Wikidata:Q54609452 |
CVCL_8B52 | 2026-08-01 05:57:37 | 0 | ||||
|
AG01262 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE41 | Homo sapiens (Human) | Retinoblastoma | PMID:7253718 | Finite cell line | Female | AG-1262, AG 1262, AG1262 | Coriell:AG01262, Wikidata:Q54609427 |
CVCL_JE41 | 2026-08-01 05:57:36 | 0 | |||||
|
AG-F Resource Report Resource Website Contaminated Discontinued |
RRID:CVCL_D101 | Homo sapiens (Human) | Childhood T acute lymphoblastic leukemia | Population: Caucasian., Problematic cell line: Contaminated. Shown to be a CCRF-CEM derivative (PubMed=12592342; PubMed=20143388). Originally thought to originates from the bone marrow of a patient suffering from neuroblastoma that evolved into a Hodgkin lymphoma.., Group: Patented cell line. |
PMID:8255104 PMID:12592342 PMID:20143388 PMID:29533902 |
Cancer cell line | Female | AGF | ATCC:CRL-2530, BioSample:SAMN03151617, BioSample:SAMN03471608, cancercelllines:CVCL_D101, Wikidata:Q54609413 |
cvcl_0207 | CVCL_D101 | 2026-08-01 05:57:35 | 0 | |||
|
AG01839 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE28 | Homo sapiens (Human) | Population: South American (Brazil, Guyana, Venezuela). | PMID:7253718 | Finite cell line | Female | AG-1839, AG 1839, AG1839 | Coriell:AG01839, Wikidata:Q54609529 |
CVCL_JE28 | 2026-08-01 05:57:36 | 0 | |||||
|
AG0150 Resource Report Resource Website Discontinued |
RRID:CVCL_8B50 | Homo sapiens (Human) | Alagille syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:90081516, Wikidata:Q54609443 |
CVCL_8B50 | 2026-08-01 05:57:35 | 0 | ||||||
|
AG0150 Resource Report Resource Website Discontinued |
ECACC Cat# 90081516, RRID:CVCL_8B50 | Homo sapiens (Human) | Alagille syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90081516 | ECACC:90081516, Wikidata:Q54609443 |
CVCL_8B50 | 2026-08-01 05:57:35 | 0 | ||||
|
AG01839 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG01839, RRID:CVCL_JE28 | Homo sapiens (Human) | Population: South American (Brazil, Guyana, Venezuela). | PMID:7253718 | Finite cell line | Female | AG-1839, AG 1839, AG1839 | Coriell | AG01839 | Coriell:AG01839, Wikidata:Q54609529 |
CVCL_JE28 | 2026-08-01 05:57:38 | 0 | |||
|
AG0124 Resource Report Resource Website Discontinued |
ECACC Cat# 90052207, RRID:CVCL_8B47 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90052207 | ECACC:90052207, Wikidata:Q54609426 |
CVCL_8B47 | 2026-08-01 05:57:35 | 0 | ||||
|
AG00781 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_W842 | Homo sapiens (Human) | Progeria | Finite cell line | AG0781B | Coriell:AG00781, Wikidata:Q54609419 |
CVCL_W842 | 2026-08-01 05:57:36 | 0 | |||||||
|
AG01517 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2KS | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Female | AG1517 | Coriell:AG01517, Wikidata:Q105506064 |
CVCL_A2KS | 2026-08-01 05:57:36 | 0 |
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