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.
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WI
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM16292, RRID:CVCL_A5WI Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WL
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM16295, RRID:CVCL_A5WL Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WK
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5WK Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WC
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5WC Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WD
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5WD Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WH
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5WH Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WL
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5WL Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WM
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5WM Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A5WR
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM16330, RRID:CVCL_A5WR Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_0H58
Organism: Homo sapiens (Human)
Disease: Tourette syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_0H58 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_0H57
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM16434, RRID:CVCL_0H57 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_0H58
Organism: Homo sapiens (Human)
Disease: Tourette syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM16436, RRID:CVCL_0H58 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_YP91
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_YP91 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_YP91
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM16733, RRID:CVCL_YP91 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_YP92
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM16735, RRID:CVCL_YP92 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_9Z53
Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 7B
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_9Z53 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_H530
Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Finite cell line
Comments: Senescence: Capable of at least 32 PDL (Coriell=GM17731).
Proper citation: RRID:CVCL_H530 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_1U26
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi., Part of: National Laboratory for the Genetics of Israeli Populations (NLGIP) collection.
Proper citation: Coriell Cat# GM22232, RRID:CVCL_1U26 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_5V23
Organism: Homo sapiens (Human)
Disease: Angelman syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5V23 Copy
Misclassified Misclassified Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_H616
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Characteristics: Secretes IgG2 kappa., Population: Caucasian., Problematic cell line: Misclassified. Parent cell line (GM01500) was originally thought to be a myeloma cell line but is a B-lymphoblastoid cell line.., Group: Patented cell line., Group: Hybridoma fusion partner cell line.
Proper citation: RRID:CVCL_H616 Copy
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Data set from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings."
