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_9N54
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01060516, RRID:CVCL_9N54 Copy
https://web.expasy.org/cellosaurus/CVCL_9N32
Organism: Homo sapiens (Human)
Disease: Aniridia
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00081102, RRID:CVCL_9N32 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q24
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XX,t18 (ECACC=01081517)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q24 Copy
https://web.expasy.org/cellosaurus/CVCL_9N44
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,inv(9)(q?13;q22.33)pat (ECACC=01011217)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N44 Copy
https://web.expasy.org/cellosaurus/CVCL_9N55
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX.ish 22q11.2(cH748x2) (ECACC=01081516)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01081516, RRID:CVCL_9N55 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q12
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX t(5;13)(p15.1;q32.3)pat (ECACC=01040309)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01040309, RRID:CVCL_9Q12 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q21
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+I(18p); de novo (ECACC=01062518)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q21 Copy
https://web.expasy.org/cellosaurus/CVCL_9N36
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00101121, RRID:CVCL_9N36 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q19
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01052919, RRID:CVCL_9Q19 Copy
https://web.expasy.org/cellosaurus/CVCL_9N39
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00111602, RRID:CVCL_9N39 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q14
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01052221, RRID:CVCL_9Q14 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q19
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q19 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q10
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,X,del(X)(q21.3) (ECACC=01011713)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q10 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q39
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q39 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q30
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(10,22)(q24.3;q13.31) (ECACC=02030406)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q30 Copy
https://web.expasy.org/cellosaurus/CVCL_9N58
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,dup(15)(pter->q15::q11.2->q13::q15->qter) (ECACC=01111321)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01111321, RRID:CVCL_9N58 Copy
https://web.expasy.org/cellosaurus/CVCL_9N64
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,inv ins(9;2)(9p;2q3.?3->2q31) (ECACC=01111421)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N64 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_2885
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_2885 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q43
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q43 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q28
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(10;18)?(q21.2;q12.2); de novo (ECACC=01092723)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01092723, RRID:CVCL_9Q28 Copy
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