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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
TT0113 Resource Report Resource Website Discontinued |
ECACC Cat# 90062723, RRID:CVCL_8Y80 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90062723 | ECACC:90062723, Wikidata:Q54973187 |
CVCL_8Y80 | 2026-07-25 05:03:46 | 0 | |||||
|
TT0114 Resource Report Resource Website Discontinued |
ECACC Cat# 90062724, RRID:CVCL_8Y81 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90062724 | ECACC:90062724, Wikidata:Q54973188 |
CVCL_8Y81 | 2026-07-25 05:03:46 | 0 | ||||
|
TT0208 Resource Report Resource Website Discontinued |
ECACC Cat# 91042501, RRID:CVCL_8Y94 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91042501 | ECACC:91042501, Wikidata:Q54973209 |
CVCL_8Y94 | 2026-07-25 05:03:47 | 0 | |||||
|
TT0148 Resource Report Resource Website Discontinued |
ECACC Cat# 91012408, RRID:CVCL_8Y84 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012408 | ECACC:91012408, Wikidata:Q54973196 |
CVCL_8Y84 | 2026-07-25 05:03:46 | 0 | ||||
|
TT0154 Resource Report Resource Website Discontinued |
ECACC Cat# 91012414, RRID:CVCL_8Y88 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012414 | ECACC:91012414, Wikidata:Q54973201 |
CVCL_8Y88 | 2026-07-25 05:03:46 | 0 | ||||
|
TT0151 Resource Report Resource Website Discontinued |
ECACC Cat# 91012411, RRID:CVCL_8Y86 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012411 | ECACC:91012411, Wikidata:Q54973198 |
CVCL_8Y86 | 2026-07-25 05:03:46 | 0 | ||||
|
TT0115 Resource Report Resource Website Discontinued |
ECACC Cat# 90062725, RRID:CVCL_8Y82 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90062725 | ECACC:90062725, Wikidata:Q54973189 |
CVCL_8Y82 | 2026-07-25 05:03:46 | 0 | ||||
|
TT0112 Resource Report Resource Website Discontinued |
ECACC Cat# 90062722, RRID:CVCL_8Y79 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90062722 | ECACC:90062722, Wikidata:Q54973186 |
CVCL_8Y79 | 2026-07-25 05:03:46 | 0 | |||||
|
TT0209 Resource Report Resource Website Discontinued |
ECACC Cat# 91042502, RRID:CVCL_8Y95 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91042502 | ECACC:91042502, Wikidata:Q54973210 |
CVCL_8Y95 | 2026-07-25 05:03:47 | 0 | |||||
|
TT0211 Resource Report Resource Website Discontinued |
ECACC Cat# 91042504, RRID:CVCL_8Y97 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91042504 | ECACC:91042504, Wikidata:Q54973212 |
CVCL_8Y97 | 2026-07-25 05:03:47 | 0 | |||||
|
TT0237 Resource Report Resource Website Discontinued |
ECACC Cat# 91062105, RRID:CVCL_8Y99 | Homo sapiens (Human) | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91062105 | ECACC:91062105, Wikidata:Q54973214 |
CVCL_8Y99 | 2026-07-25 05:03:47 | 0 | |||||
|
TT0153 Resource Report Resource Website Discontinued |
ECACC Cat# 91012413, RRID:CVCL_8Y87 | Homo sapiens (Human) | Fragile X syndrome | Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012413 | ECACC:91012413, Wikidata:Q54973199 |
CVCL_8Y87 | 2026-07-25 05:03:46 | 0 | ||||
|
TTDHM1BR LCL Resource Report Resource Website |
ECACC Cat# 98062320, RRID:CVCL_2554 | Homo sapiens (Human) | Transformed cell line | Female | TrichoThioDystrophy Heterozygote Mother 1 BRighton LCL, LB198, 198 | ECACC | 98062320 | ECACC:98062320, Wikidata:Q54902042 |
CVCL_2554 | 2026-07-25 05:03:49 | 0 | |||||
|
UKBi006-A Resource Report Resource Website |
ECACC Cat# 66540004, RRID:CVCL_1E86 | Homo sapiens (Human) | Population: Caucasian; German., From: Institut fur Rekonstruktive Neurobiologie, University Clinic of Bonn; Bonn; Germany. | Induced pluripotent stem cell | Male | iLB-C-35m-R1, LB-35-1 | ECACC | 66540004 | BioSamples:SAMEA2590936, EBiSC:UKBi006-A, ECACC:66540004, hPSCreg:UKBi006-A, SKIP:SKIP002509, Wikidata:Q54990265 |
CVCL_1E86 | 2026-07-25 05:04:23 | 0 | ||||
|
UKBi005-A Resource Report Resource Website |
ECACC Cat# 66540008, RRID:CVCL_1E85 | Homo sapiens (Human) | From: Institut fur Rekonstruktive Neurobiologie, University Clinic of Bonn; Bonn; Germany. | Induced pluripotent stem cell | Female | iLB-C-31f-r1, iLB-C-31f-R1, LB-31-1 | ECACC | 66540008 | BioSamples:SAMEA4584351, EBiSC:UKBi005-A, ECACC:66540008, hPSCreg:UKBi005-A, SKIP:SKIP002508, Wikidata:Q54990251 |
CVCL_1E85 | 2026-07-25 05:04:23 | 0 | ||||
|
UKKi021-B Resource Report Resource Website |
ECACC Cat# 66540565, RRID:CVCL_LD32 | Homo sapiens (Human) | Population: Indian., From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany. | Induced pluripotent stem cell | Male | NP0105-19 | ECACC | 66540565 | BioSamples:SAMEA103988346, EBiSC:UKKi021-B, ECACC:66540565, EGA:EGAS00001002755, hPSCreg:UKKi021-B, Wikidata:Q54990479 |
CVCL_LD32 | 2026-07-25 05:04:25 | 0 | ||||
|
UKKi006-A Resource Report Resource Website |
ECACC Cat# 66540018, RRID:CVCL_9S59 | Homo sapiens (Human) | Population: Caucasian., From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany. | PMID:23032973 | Induced pluripotent stem cell | Female | NP0053-5, M4C4, iP-MSC D4 cB, D4-CB, D4-cB, iP-MSC donor 4 clone B | ECACC | 66540018 | BioSamples:SAMEA2825851, EBiSC:UKKi006-A, ECACC:66540018, hPSCreg:UKKi006-A, SKIP:SKIP002458, Wikidata:Q54990421 |
CVCL_9S59 | 2026-07-25 05:04:24 | 0 | |||
|
UKKi026-C Resource Report Resource Website |
ECACC Cat# 66540596, RRID:CVCL_LD47 | Homo sapiens (Human) | Population: Chinese., From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany. | Induced pluripotent stem cell | Male | NP0114-5E | ECACC | 66540596 | BioSamples:SAMEA104132933, EBiSC:UKKi026-C, ECACC:66540596, hPSCreg:UKKi026-C, Wikidata:Q54990496 |
CVCL_LD47 | 2026-07-25 05:04:26 | 0 | ||||
|
UKKi024-B Resource Report Resource Website |
ECACC Cat# 66540489, RRID:CVCL_LD85 | Homo sapiens (Human) | Brugada syndrome | Population: Caucasian., From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany. | Induced pluripotent stem cell | Male | NP0133-1 | ECACC | 66540489 | BioSamples:SAMEA17635168, EBiSC:UKKi024-B, ECACC:66540489, hPSCreg:UKKi024-B, Wikidata:Q54990488 |
CVCL_LD85 | 2026-07-25 05:04:25 | 0 | |||
|
UKKi022-C Resource Report Resource Website |
ECACC Cat# 66540568, RRID:CVCL_LD35 | Homo sapiens (Human) | Population: Indian., From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany. | Induced pluripotent stem cell | Female | NP0106-10A | ECACC | 66540568 | BioSamples:SAMEA103988349, EBiSC:UKKi022-C, ECACC:66540568, EGA:EGAS00001002755, hPSCreg:UKKi022-C, Wikidata:Q54990482 |
CVCL_LD35 | 2026-07-25 05:04:25 | 0 |
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