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.
https://web.expasy.org/cellosaurus/CVCL_8A72
Organism: Homo sapiens (Human)
Disease: Farber lipogranulomatosis
Category: Finite cell line
Comments: Population: Caucasian; Belgian.
Proper citation: RRID:CVCL_8A72 Copy
https://web.expasy.org/cellosaurus/CVCL_K263
Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Finite cell line
Comments: Population: Japanese.
Proper citation: RCB Cat# RCB0697, RRID:CVCL_K263 Copy
https://web.expasy.org/cellosaurus/CVCL_9R97
Organism: Homo sapiens (Human)
Disease: Mucolipidosis type IIIA
Category: Finite cell line
Proper citation: RRID:CVCL_9R97 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_F637
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_F637 Copy
https://web.expasy.org/cellosaurus/CVCL_9R56
Organism: Homo sapiens (Human)
Disease: Autism spectrum disorder
Category: Transformed cell line
Proper citation: RRID:CVCL_9R56 Copy
https://web.expasy.org/cellosaurus/CVCL_5R03
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_5R03 Copy
https://web.expasy.org/cellosaurus/CVCL_DA80
Organism: Homo sapiens (Human)
Disease: Congenital disorder of glycosylation type Ig
Category: Finite cell line
Proper citation: RRID:CVCL_DA80 Copy
https://web.expasy.org/cellosaurus/CVCL_N880
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.
Proper citation: RRID:CVCL_N880 Copy
https://web.expasy.org/cellosaurus/CVCL_N879
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.
Proper citation: Coriell Cat# GM19982, RRID:CVCL_N879 Copy
https://web.expasy.org/cellosaurus/CVCL_2N06
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_2N06 Copy
https://web.expasy.org/cellosaurus/CVCL_GS92
Organism: Homo sapiens (Human)
Disease: Deafness, autosomal recessive 49
Category: Transformed cell line
Comments: Population: Pakistani.
Proper citation: RRID:CVCL_GS92 Copy
https://web.expasy.org/cellosaurus/CVCL_9Y53
Organism: Homo sapiens (Human)
Disease: Donohue syndrome
Category: Finite cell line
Comments: Population: Kurdistani.
Proper citation: RRID:CVCL_9Y53 Copy
https://web.expasy.org/cellosaurus/CVCL_DB95
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_DB95 Copy
https://web.expasy.org/cellosaurus/CVCL_8A73
Organism: Homo sapiens (Human)
Disease: Farber lipogranulomatosis
Category: Finite cell line
Proper citation: RRID:CVCL_8A73 Copy
https://web.expasy.org/cellosaurus/CVCL_F105
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_F105 Copy
https://web.expasy.org/cellosaurus/CVCL_N879
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.
Proper citation: RRID:CVCL_N879 Copy
https://web.expasy.org/cellosaurus/CVCL_A3YY
Organism: Homo sapiens (Human)
Disease: Galloway-Mowat syndrome
Category: Induced pluripotent stem cell
Comments: Population: Asian.
Proper citation: RRID:CVCL_A3YY Copy
https://web.expasy.org/cellosaurus/CVCL_5R05
Organism: Homo sapiens (Human)
Disease: Autism spectrum disorder
Category: Transformed cell line
Proper citation: Coriell Cat# GM20201, RRID:CVCL_5R05 Copy
https://web.expasy.org/cellosaurus/CVCL_DA81
Organism: Homo sapiens (Human)
Disease: Congenital disorder of glycosylation type Ig
Category: Finite cell line
Proper citation: RRID:CVCL_DA81 Copy
https://web.expasy.org/cellosaurus/CVCL_N880
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.
Proper citation: Coriell Cat# GM19984, RRID:CVCL_N880 Copy
Can't find your Cell Line?
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