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_9P43
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9P43 Copy
https://web.expasy.org/cellosaurus/CVCL_9P61
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 99060326, RRID:CVCL_9P61 Copy
https://web.expasy.org/cellosaurus/CVCL_9P58
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 99052013, RRID:CVCL_9P58 Copy
https://web.expasy.org/cellosaurus/CVCL_9P56
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 99051301, RRID:CVCL_9P56 Copy
https://web.expasy.org/cellosaurus/CVCL_9P54
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9P54 Copy
https://web.expasy.org/cellosaurus/CVCL_9M99
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 99021006, RRID:CVCL_9M99 Copy
https://web.expasy.org/cellosaurus/CVCL_9P69
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 99081611, RRID:CVCL_9P69 Copy
https://web.expasy.org/cellosaurus/CVCL_9M95
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 98122306, RRID:CVCL_9M95 Copy
https://web.expasy.org/cellosaurus/CVCL_9N18
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00031407, RRID:CVCL_9N18 Copy
https://web.expasy.org/cellosaurus/CVCL_9N10
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,inv(4)(q15.32;q13.2)pat (ECACC=99102831)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 99102831, RRID:CVCL_9N10 Copy
https://web.expasy.org/cellosaurus/CVCL_9P79
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+mar (ECACC=00013124)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9P79 Copy
https://web.expasy.org/cellosaurus/CVCL_9P91
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00032003, RRID:CVCL_9P91 Copy
https://web.expasy.org/cellosaurus/CVCL_9N26
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(7;18)(q11.2;q23) (ECACC=00050802)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N26 Copy
https://web.expasy.org/cellosaurus/CVCL_9N10
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,inv(4)(q15.32;q13.2)pat (ECACC=99102831)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N10 Copy
https://web.expasy.org/cellosaurus/CVCL_9P95
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,X,del(X)(qter->p22.31 or p22.32) (ECACC=00060704)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00060704, RRID:CVCL_9P95 Copy
https://web.expasy.org/cellosaurus/CVCL_9N15
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,Y,add(X)(q28) (ECACC=00022418)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N15 Copy
https://web.expasy.org/cellosaurus/CVCL_9P92
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00041222, RRID:CVCL_9P92 Copy
https://web.expasy.org/cellosaurus/CVCL_9N19
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N19 Copy
https://web.expasy.org/cellosaurus/CVCL_9P74
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9P74 Copy
https://web.expasy.org/cellosaurus/CVCL_9P78
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9P78 Copy
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