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_9P72
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(10;11)(q24.?31;p15.5); de novo (ECACC=99092423)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 99092423, RRID:CVCL_9P72 Copy
https://web.expasy.org/cellosaurus/CVCL_9N11
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(5;13)(p11;p12) (ECACC=99112428)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N11 Copy
https://web.expasy.org/cellosaurus/CVCL_9N24
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00050408, RRID:CVCL_9N24 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: ECACC Cat# 99102243, RRID:CVCL_9P74 Copy
https://web.expasy.org/cellosaurus/CVCL_9N23
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(11;22)(23.3;q11.2)mat (ECACC=00050205)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N23 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: RRID:CVCL_9P92 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q16
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,add(1)(p?36.2) (ECACC=01052422)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9Q16 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: RRID:CVCL_9Q12 Copy
https://web.expasy.org/cellosaurus/CVCL_9N33
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(5;11)(q13.1;p15.1)mat (ECACC=00090409)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N33 Copy
https://web.expasy.org/cellosaurus/CVCL_9N38
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N38 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q01
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XXX (ECACC=00081509)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00081509, RRID:CVCL_9Q01 Copy
https://web.expasy.org/cellosaurus/CVCL_9N41
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9N41 Copy
https://web.expasy.org/cellosaurus/CVCL_9N40
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00112301, RRID:CVCL_9N40 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: RRID:CVCL_9N55 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q06
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00112701, RRID:CVCL_9Q06 Copy
https://web.expasy.org/cellosaurus/CVCL_9N53
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+der(15)t(11;15)mat (ECACC=01060418)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01060418, RRID:CVCL_9N53 Copy
https://web.expasy.org/cellosaurus/CVCL_9Q16
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,add(1)(p?36.2) (ECACC=01052422)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01052422, RRID:CVCL_9Q16 Copy
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_9N65
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01070531, RRID:CVCL_9N65 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
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