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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD0142 Resource Report Resource Website |
ECACC Cat# 91011606, RRID:CVCL_8U85 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91011606 | ECACC:91011606, Wikidata:Q54828773 |
CVCL_8U85 | 2026-09-12 05:29:13 | 0 | |||||
|
DD0046 Resource Report Resource Website |
ECACC Cat# 90101601, RRID:CVCL_AQ56 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 90101601 | ECACC:90101601, Wikidata:Q54828730 |
CVCL_AQ56 | 2026-09-12 05:29:12 | 0 | |||||
|
DD0140 Resource Report Resource Website |
RRID:CVCL_8U83 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:91011103, Wikidata:Q54828771 |
CVCL_8U83 | 2026-09-12 05:29:13 | 0 | |||||||
|
DD0036 Resource Report Resource Website |
ECACC Cat# 90092708, RRID:CVCL_8U44 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90092708 | ECACC:90092708, Wikidata:Q54828722 |
CVCL_8U44 | 2026-09-12 05:29:11 | 0 | |||||
|
DD0056 Resource Report Resource Website |
RRID:CVCL_8U53 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(4;9)(p16;q32)pat (ECACC=90091701)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:90091701, Wikidata:Q54828734 |
CVCL_8U53 | 2026-09-12 05:29:12 | 0 | |||||||
|
DD0084 Resource Report Resource Website |
RRID:CVCL_8U61 | Homo sapiens (Human) | Pallister-Killian syndrome | Karyotypic information: 46,XY; 47,XY,+i(12p) (ECACC=90020901)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:90020901, Wikidata:Q54828746 |
CVCL_8U61 | 2026-09-12 05:29:12 | 0 | ||||||
|
DD0084 Resource Report Resource Website |
ECACC Cat# 90020901, RRID:CVCL_8U61 | Homo sapiens (Human) | Pallister-Killian syndrome | Karyotypic information: 46,XY; 47,XY,+i(12p) (ECACC=90020901)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 90020901 | ECACC:90020901, Wikidata:Q54828746 |
CVCL_8U61 | 2026-09-12 05:29:12 | 0 | ||||
|
DD0122 Resource Report Resource Website |
ECACC Cat# 90121814, RRID:CVCL_8U76 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90121814 | ECACC:90121814, Wikidata:Q54828764 |
CVCL_8U76 | 2026-09-12 05:29:12 | 0 | |||||
|
DD0104 Resource Report Resource Website |
RRID:CVCL_8U70 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:88122801, Wikidata:Q54828756 |
CVCL_8U70 | 2026-09-12 05:29:12 | 0 | |||||||
|
DD0033 Resource Report Resource Website |
ECACC Cat# 90092604, RRID:CVCL_8U42 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90092604 | ECACC:90092604, Wikidata:Q54828720 |
CVCL_8U42 | 2026-09-12 05:29:11 | 0 | |||||
|
DD0133 Resource Report Resource Website |
RRID:CVCL_8U81 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:91010902, Wikidata:Q54828769 |
CVCL_8U81 | 2026-09-12 05:29:12 | 0 | |||||||
|
DD0051 Resource Report Resource Website |
RRID:CVCL_8U51 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:90110201, Wikidata:Q54828732 |
CVCL_8U51 | 2026-09-12 05:29:12 | 0 | |||||||
|
DD0105 Resource Report Resource Website |
RRID:CVCL_8U71 | Homo sapiens (Human) | Methylmalonic acidemia | Karyotypic information: 46,XY,fra(X)(q28) 16/50 (ECACC=88101401)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:88101401, Wikidata:Q54828758 |
CVCL_8U71 | 2026-09-12 05:29:12 | 0 | ||||||
|
DD0126 Resource Report Resource Website |
ECACC Cat# 90122403, RRID:CVCL_8U77 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90122403 | ECACC:90122403, Wikidata:Q54828765 |
CVCL_8U77 | 2026-09-12 05:29:12 | 0 | |||||
|
DD0054 Resource Report Resource Website |
RRID:CVCL_8U52 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:90112722, Wikidata:Q54828733 |
CVCL_8U52 | 2026-09-12 05:29:12 | 0 | |||||||
|
DD0171 Resource Report Resource Website |
ECACC Cat# 91020711, RRID:CVCL_8U97 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91020711 | ECACC:91020711, Wikidata:Q54828797 |
CVCL_8U97 | 2026-09-12 05:29:13 | 0 | ||||
|
DD0147 Resource Report Resource Website |
ECACC Cat# 91011611, RRID:CVCL_8U90 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91011611 | ECACC:91011611, Wikidata:Q54828779 |
CVCL_8U90 | 2026-09-12 05:29:13 | 0 | |||||
|
DD0210 Resource Report Resource Website |
RRID:CVCL_8V25 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:91032004, Wikidata:Q54828826 |
CVCL_8V25 | 2026-09-12 05:29:14 | 0 | ||||||
|
DD0186 Resource Report Resource Website |
ECACC Cat# 91022220, RRID:CVCL_8V08 | Homo sapiens (Human) | Karyotypic information: 46,XY,?dup(1)(q32->q42.1) (ECACC=91022220)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 91022220 | ECACC:91022220, Wikidata:Q54828808 |
CVCL_8V08 | 2026-09-12 05:29:13 | 0 | |||||
|
DD0223 Resource Report Resource Website |
ECACC Cat# 91032713, RRID:CVCL_8V32 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91032713 | ECACC:91032713, Wikidata:Q54828833 |
CVCL_8V32 | 2026-09-12 05:29:14 | 0 |
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