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_BA19
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_BA19 Copy
https://web.expasy.org/cellosaurus/CVCL_HL85
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HL85 Copy
https://web.expasy.org/cellosaurus/CVCL_5K77
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5K77 Copy
https://web.expasy.org/cellosaurus/CVCL_5K89
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25374, RRID:CVCL_5K89 Copy
https://web.expasy.org/cellosaurus/CVCL_5K92
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25378, RRID:CVCL_5K92 Copy
https://web.expasy.org/cellosaurus/CVCL_5K84
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25367, RRID:CVCL_5K84 Copy
https://web.expasy.org/cellosaurus/CVCL_5K85
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5K85 Copy
https://web.expasy.org/cellosaurus/CVCL_JF32
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_JF32 Copy
https://web.expasy.org/cellosaurus/CVCL_1N94
Organism: Homo sapiens (Human)
Disease: Long QT syndrome 2
Category: Induced pluripotent stem cell
Comments: Population: Chinese.
Proper citation: RRID:CVCL_1N94 Copy
https://web.expasy.org/cellosaurus/CVCL_5K91
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5K91 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ22
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25406, RRID:CVCL_HQ22 Copy
https://web.expasy.org/cellosaurus/CVCL_5K88
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5K88 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ42
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_HQ42 Copy
https://web.expasy.org/cellosaurus/CVCL_GZ54
Organism: Homo sapiens (Human)
Disease: Microcephaly and chorioretinopathy, autosomal recessive, type 1
Category: Finite cell line
Comments: Population: Caucasian; Mennonite.
Proper citation: RRID:CVCL_GZ54 Copy
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_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_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_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
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