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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD0007 Resource Report Resource Website |
ECACC Cat# 90041701, RRID:CVCL_8U29 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90041701 | ECACC:90041701, Wikidata:Q54828707 |
CVCL_8U29 | 2026-08-29 04:24:39 | 0 | |||||
|
DD0019 Resource Report Resource Website |
ECACC Cat# 90031301, RRID:CVCL_8U33 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90031301 | ECACC:90031301, Wikidata:Q54828711 |
CVCL_8U33 | 2026-08-29 04:24:33 | 0 | |||||
|
DD0014 Resource Report Resource Website |
ECACC Cat# 90012301, RRID:CVCL_8U31 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90012301 | ECACC:90012301, Wikidata:Q54828709 |
CVCL_8U31 | 2026-08-29 04:24:33 | 0 | ||||
|
DD0026 Resource Report Resource Website |
ECACC Cat# 90060803, RRID:CVCL_8U39 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90060803 | ECACC:90060803, Wikidata:Q54828717 |
CVCL_8U39 | 2026-08-29 04:24:33 | 0 | |||||
|
DCH008 Resource Report Resource Website |
ECACC Cat# 94082284, RRID:CVCL_E552 | Homo sapiens (Human) | Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. |
PMID:8307784 PMID:30844424 |
Transformed cell line | Male | DCH 008, DCH-008, Thai-DCH008 | ECACC | 94082284 | dbMHC:48748, ECACC:94082284, IHW:IHW09184, IPD-IMGT/HLA:11726, Wikidata:Q54828660 |
CVCL_E552 | 2026-08-29 04:24:32 | 0 | |||
|
DD0021 Resource Report Resource Website |
ECACC Cat# 90042701, RRID:CVCL_8U35 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90042701 | ECACC:90042701, Wikidata:Q54828713 |
CVCL_8U35 | 2026-08-29 04:24:39 | 0 | |||||
|
DD0017 Resource Report Resource Website |
ECACC Cat# 90021605, RRID:CVCL_8U32 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90021605 | ECACC:90021605, Wikidata:Q54828710 |
CVCL_8U32 | 2026-08-29 04:24:39 | 0 | |||||
|
DD0012 Resource Report Resource Website |
ECACC Cat# 90010801, RRID:CVCL_8U30 | Homo sapiens (Human) | Karyotypic information: 46,XY,inv(6)(p21.33;q23.3),t(7;13) (ECACC=90010801)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90010801 | ECACC:90010801, Wikidata:Q54828708 |
CVCL_8U30 | 2026-08-29 04:24:33 | 0 | |||||
|
DCH011 Resource Report Resource Website |
ECACC Cat# 94082286, RRID:CVCL_E556 | Homo sapiens (Human) | Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. |
PMID:8307784 PMID:30844424 |
Transformed cell line | Female | DCH 011, DCH-011, Thai-DCH011, THAI DCH011 | ECACC | 94082286 | dbMHC:48751, ECACC:94082286, IHW:IHW09186, IPD-IMGT/HLA:11728, Wikidata:Q54828663 |
CVCL_E556 | 2026-08-29 04:24:32 | 0 | |||
|
DCH012 Resource Report Resource Website |
ECACC Cat# 94082287, RRID:CVCL_E558 | Homo sapiens (Human) | Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. |
PMID:8307784 PMID:30844424 |
Transformed cell line | Male | DCH 012, DCH-012, Thai-DCH012, THAI DCH012 | ECACC | 94082287 | dbMHC:48752, ECACC:94082287, IHW:IHW09187, IPD-IMGT/HLA:11729, Wikidata:Q54828664 |
CVCL_E558 | 2026-08-29 04:24:39 | 0 | |||
|
DCH007 Resource Report Resource Website |
ECACC Cat# 94082283, RRID:CVCL_E551 | Homo sapiens (Human) | Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. |
PMID:8307784 PMID:30844424 |
Transformed cell line | Male | DCH 007, DCH-007, Thai-DCH007 | ECACC | 94082283 | dbMHC:48747, ECACC:94082283, IHW:IHW09183, IPD-IMGT/HLA:11725, Wikidata:Q54828659 |
CVCL_E551 | 2026-08-29 04:24:32 | 0 | |||
|
DD0106 Resource Report Resource Website |
ECACC Cat# 88052403, RRID:CVCL_8U72 | Homo sapiens (Human) | Karyotypic information: 46,XY,19q+mat (ECACC=88052403)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 88052403 | ECACC:88052403, Wikidata:Q54828759 |
CVCL_8U72 | 2026-08-29 04:24:40 | 0 | |||||
|
DD0145 Resource Report Resource Website |
ECACC Cat# 91011609, RRID:CVCL_8U88 | Homo sapiens (Human) | Angelman syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91011609 | ECACC:91011609, Wikidata:Q54828777 |
CVCL_8U88 | 2026-08-29 04:24:34 | 0 | ||||
|
DD0141 Resource Report Resource Website |
ECACC Cat# 91011506, RRID:CVCL_8U84 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91011506 | ECACC:91011506, Wikidata:Q54828772 |
CVCL_8U84 | 2026-08-29 04:24:40 | 0 | |||||
|
DD0072 Resource Report Resource Website |
ECACC Cat# 90060402, RRID:CVCL_8U58 | Homo sapiens (Human) | Karyotypic information: 46,XX; 47,XX,+18 (ECACC=90060402)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90060402 | ECACC:90060402, Wikidata:Q54828743 |
CVCL_8U58 | 2026-08-29 04:24:34 | 0 | |||||
|
DD0058 Resource Report Resource Website |
ECACC Cat# 90090604, RRID:CVCL_8U55 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90090604 | ECACC:90090604, Wikidata:Q54828740 |
CVCL_8U55 | 2026-08-29 04:24:34 | 0 | ||||
|
DD0051 Resource Report Resource Website |
ECACC Cat# 90110201, RRID:CVCL_8U51 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90110201 | ECACC:90110201, Wikidata:Q54828732 |
CVCL_8U51 | 2026-08-29 04:24:39 | 0 | |||||
|
DD0073 Resource Report Resource Website |
ECACC Cat# 90042503, RRID:CVCL_8U59 | Homo sapiens (Human) | Karyotypic information: 46,XX; 47,XX,+mar mat (ECACC=90042503)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90042503 | ECACC:90042503, Wikidata:Q54828744 |
CVCL_8U59 | 2026-08-29 04:24:34 | 0 | |||||
|
DD0098 Resource Report Resource Website |
ECACC Cat# 89070501, RRID:CVCL_8U66 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89070501 | ECACC:89070501, Wikidata:Q54828751 |
CVCL_8U66 | 2026-08-29 04:24:40 | 0 | ||||
|
DD0108 Resource Report Resource Website |
ECACC Cat# 870424011, RRID:CVCL_8U73 | Homo sapiens (Human) | Karyotypic information: 47,XX,+dic(15)(pter->q11::q11->pter) (ECACC=870424011)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 870424011 | ECACC:870424011, Wikidata:Q54828760 |
CVCL_8U73 | 2026-08-29 04:24:34 | 0 |
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