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_AZ44
Organism: Homo sapiens (Human)
Disease: Argininosuccinic aciduria
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25500, RRID:CVCL_AZ44 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ46
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HQ46 Copy
https://web.expasy.org/cellosaurus/CVCL_EH28
Organism: Homo sapiens (Human)
Disease: Choroideremia
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_EH28 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ27
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HQ27 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ50
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25544, RRID:CVCL_HQ50 Copy
https://web.expasy.org/cellosaurus/CVCL_AY58
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_AY58 Copy
https://web.expasy.org/cellosaurus/CVCL_CX90
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: RRID:CVCL_CX90 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ34
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_HQ34 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ45
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25483, RRID:CVCL_HQ45 Copy
https://web.expasy.org/cellosaurus/CVCL_HL86
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25412, RRID:CVCL_HL86 Copy
https://web.expasy.org/cellosaurus/CVCL_5T44
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Induced pluripotent stem cell
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5T44 Copy
https://web.expasy.org/cellosaurus/CVCL_LN96
Organism: Homo sapiens (Human)
Disease: Potocki-Lupski syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_LN96 Copy
https://web.expasy.org/cellosaurus/CVCL_JF33
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25522, RRID:CVCL_JF33 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ26
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HQ26 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ33
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25434, RRID:CVCL_HQ33 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ36
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25437, RRID:CVCL_HQ36 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ40
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25451, RRID:CVCL_HQ40 Copy
https://web.expasy.org/cellosaurus/CVCL_CX88
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: Coriell Cat# GM25441, RRID:CVCL_CX88 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ43
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25454, RRID:CVCL_HQ43 Copy
https://web.expasy.org/cellosaurus/CVCL_CX91
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: RRID:CVCL_CX91 Copy
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