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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD2870 Resource Report Resource Website |
ECACC Cat# 97032105, RRID:CVCL_9L36 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97032105 | ECACC:97032105, Wikidata:Q54830444 |
CVCL_9L36 | 2026-08-15 04:26:56 | 0 | ||||
|
DD2896 Resource Report Resource Website |
ECACC Cat# 97043012, RRID:CVCL_9L48 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(14;16)(q24;q11.1) (ECACC=97043012)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97043012 | ECACC:97043012, Wikidata:Q54830458 |
CVCL_9L48 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2938 Resource Report Resource Website |
ECACC Cat# 97071612, RRID:CVCL_9L65 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97071612 | ECACC:97071612, Wikidata:Q54830478 |
CVCL_9L65 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2891 Resource Report Resource Website |
ECACC Cat# 97042203, RRID:CVCL_9L47 | Homo sapiens (Human) | Karyotypic information: 46,XX,der(13)inv(13)(q31.2;q32.3)t(13;18)(q32.3;q23)mat (ECACC=97042203)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97042203 | ECACC:97042203, Wikidata:Q54830456 |
CVCL_9L47 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2930 Resource Report Resource Website |
ECACC Cat# 97070208, RRID:CVCL_9L63 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97070208 | ECACC:97070208, Wikidata:Q54830475 |
CVCL_9L63 | 2026-08-15 04:26:57 | 0 | ||||
|
DD2871 Resource Report Resource Website |
ECACC Cat# 97032501, RRID:CVCL_9L37 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97032501 | ECACC:97032501, Wikidata:Q54830445 |
CVCL_9L37 | 2026-08-15 04:26:56 | 0 | ||||
|
DD2868 Resource Report Resource Website |
ECACC Cat# 97031817, RRID:CVCL_9L35 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97031817 | ECACC:97031817, Wikidata:Q54830443 |
CVCL_9L35 | 2026-08-15 04:26:57 | 0 | ||||
|
DD2856 Resource Report Resource Website |
ECACC Cat# 97022603, RRID:CVCL_AR33 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97022603 | ECACC:97022603, Wikidata:Q54830434 |
CVCL_AR33 | 2026-08-15 04:26:56 | 0 | |||||
|
DD2943 Resource Report Resource Website |
ECACC Cat# 97071617, RRID:CVCL_9L68 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97071617 | ECACC:97071617, Wikidata:Q54830484 |
CVCL_9L68 | 2026-08-15 04:26:58 | 0 | |||||
|
DD2884 Resource Report Resource Website |
ECACC Cat# 97041711, RRID:CVCL_9L44 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97041711 | ECACC:97041711, Wikidata:Q54830453 |
CVCL_9L44 | 2026-08-15 04:26:57 | 0 | ||||
|
DD2885 Resource Report Resource Website |
ECACC Cat# 97041801, RRID:CVCL_9L45 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97041801 | ECACC:97041801, Wikidata:Q54830454 |
CVCL_9L45 | 2026-08-15 04:26:57 | 0 | ||||
|
DD3024 Resource Report Resource Website |
ECACC Cat# 97121507, RRID:CVCL_9N67 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 97121507 | ECACC:97121507, Wikidata:Q54830519 |
CVCL_9N67 | 2026-08-15 04:26:58 | 0 | |||||
|
DD2965 Resource Report Resource Website |
ECACC Cat# 97081302, RRID:CVCL_AR37 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97081302 | ECACC:97081302, Wikidata:Q54830491 |
CVCL_AR37 | 2026-08-15 04:26:58 | 0 | |||||
|
DD2994 Resource Report Resource Website |
ECACC Cat# 97101704, RRID:CVCL_9L83 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97101704 | ECACC:97101704, Wikidata:Q54830504 |
CVCL_9L83 | 2026-08-15 04:26:58 | 0 | |||||
|
DD2986 Resource Report Resource Website |
ECACC Cat# 97100212, RRID:CVCL_AR39 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97100212 | ECACC:97100212, Wikidata:Q54830499 |
CVCL_AR39 | 2026-08-15 04:26:58 | 0 | |||||
|
DD3007 Resource Report Resource Website |
ECACC Cat# 97111308, RRID:CVCL_9L89 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97111308 | ECACC:97111308, Wikidata:Q54830513 |
CVCL_9L89 | 2026-08-15 04:26:58 | 0 | ||||
|
DD2989 Resource Report Resource Website |
ECACC Cat# 97100915, RRID:CVCL_9L81 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97100915 | ECACC:97100915, Wikidata:Q54830501 |
CVCL_9L81 | 2026-08-15 04:26:58 | 0 | ||||
|
DD2955 Resource Report Resource Website |
ECACC Cat# 97072713, RRID:CVCL_9L73 | Homo sapiens (Human) | Hypogonadism | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 97072713 | ECACC:97072713, Wikidata:Q54830489 |
CVCL_9L73 | 2026-08-15 04:26:58 | 0 | ||||
|
DD3004 Resource Report Resource Website |
ECACC Cat# 97110612, RRID:CVCL_9L87 | Homo sapiens (Human) | Karyotypic information: 47,XX,+mar.ish der(22)(D22Z3+) (ECACC=97110612)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97110612 | ECACC:97110612, Wikidata:Q54830510 |
CVCL_9L87 | 2026-08-15 04:26:58 | 0 | |||||
|
DD3013 Resource Report Resource Website |
ECACC Cat# 97112204, RRID:CVCL_9L92 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97112204 | ECACC:97112204, Wikidata:Q54830516 |
CVCL_9L92 | 2026-08-15 04:26:58 | 0 |
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