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_BW52
Organism: Homo sapiens (Human)
Disease: Choroideremia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_BW52 Copy
https://web.expasy.org/cellosaurus/CVCL_5K89
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
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
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
Proper citation: Coriell Cat# GM25367, RRID:CVCL_5K84 Copy
https://web.expasy.org/cellosaurus/CVCL_5K87
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM25372, RRID:CVCL_5K87 Copy
https://web.expasy.org/cellosaurus/CVCL_5K72
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_5K72 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_EH28
Organism: Homo sapiens (Human)
Disease: Choroideremia
Category: Finite cell line
Proper citation: RRID:CVCL_EH28 Copy
https://web.expasy.org/cellosaurus/CVCL_AY58
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_AY58 Copy
https://web.expasy.org/cellosaurus/CVCL_CX90
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: RRID:CVCL_CX90 Copy
https://web.expasy.org/cellosaurus/CVCL_CX88
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: Coriell Cat# GM25441, RRID:CVCL_CX88 Copy
https://web.expasy.org/cellosaurus/CVCL_CX91
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: RRID:CVCL_CX91 Copy
https://web.expasy.org/cellosaurus/CVCL_CX90
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: Coriell Cat# GM25444, RRID:CVCL_CX90 Copy
https://web.expasy.org/cellosaurus/CVCL_EH27
Organism: Homo sapiens (Human)
Disease: Choroideremia
Category: Finite cell line
Proper citation: RRID:CVCL_EH27 Copy
https://web.expasy.org/cellosaurus/CVCL_CX89
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: RRID:CVCL_CX89 Copy
https://web.expasy.org/cellosaurus/CVCL_GZ60
Organism: Homo sapiens (Human)
Disease: Microcephaly and chorioretinopathy, autosomal recessive, type 1
Category: Finite cell line
Comments: Population: Caucasian; Mennonite.
Proper citation: RRID:CVCL_GZ60 Copy
https://web.expasy.org/cellosaurus/CVCL_WZ57
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_WZ57 Copy
https://web.expasy.org/cellosaurus/CVCL_WZ58
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: KCB Cat# KCB 86021YJ, RRID:CVCL_WZ58 Copy
https://web.expasy.org/cellosaurus/CVCL_VX31
Organism: Cyrtopodion scabrum (Rough-tailed gecko)
Category: Finite cell line
Comments: Group: Reptilian cell line.
Proper citation: RRID:CVCL_VX31 Copy
https://web.expasy.org/cellosaurus/CVCL_ZG37
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Characteristics: Has an extended lifespan due to the lentiviral transfer of Upcyte(R) proliferation genes.
Proper citation: RRID:CVCL_ZG37 Copy
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