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_9B52
Organism: Homo sapiens (Human)
Disease: Congenital hydrocephalus
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92041520, RRID:CVCL_9B52 Copy
https://web.expasy.org/cellosaurus/CVCL_9B38
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18 (ECACC=92031805)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9B38 Copy
https://web.expasy.org/cellosaurus/CVCL_9B52
Organism: Homo sapiens (Human)
Disease: Congenital hydrocephalus
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9B52 Copy
https://web.expasy.org/cellosaurus/CVCL_9B56
Organism: Homo sapiens (Human)
Disease: Congenital hydrocephalus
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9B56 Copy
https://web.expasy.org/cellosaurus/CVCL_9B44
Organism: Homo sapiens (Human)
Disease: Congenital hydrocephalus
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9B44 Copy
https://web.expasy.org/cellosaurus/CVCL_9B77
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX; 47,XX,+20 (ECACC=92050505)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92050505, RRID:CVCL_9B77 Copy
https://web.expasy.org/cellosaurus/CVCL_9B85
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9B85 Copy
https://web.expasy.org/cellosaurus/CVCL_9B84
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92051207, RRID:CVCL_9B84 Copy
https://web.expasy.org/cellosaurus/CVCL_9B81
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,inv(Y)(p11;q11.23)pat (ECACC=92051203)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92051203, RRID:CVCL_9B81 Copy
https://web.expasy.org/cellosaurus/CVCL_9C48
Organism: Homo sapiens (Human)
Disease: 49,XXXXY syndrome
Category: Finite cell line
Comments: Karyotypic information: 49,XXXXY (ECACC=92062586)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92062586, RRID:CVCL_9C48 Copy
https://web.expasy.org/cellosaurus/CVCL_9C52
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18 (ECACC=92070220)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92070220, RRID:CVCL_9C52 Copy
https://web.expasy.org/cellosaurus/CVCL_9C53
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(12;13)(q24.31;q32.3); de novo (ECACC=92070312)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92070312, RRID:CVCL_9C53 Copy
https://web.expasy.org/cellosaurus/CVCL_9C51
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY; 46,XY,inv(9)(?p21;q12); de novo (ECACC=92070219)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9C51 Copy
https://web.expasy.org/cellosaurus/CVCL_9C50
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18 (ECACC=92070113)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9C50 Copy
https://web.expasy.org/cellosaurus/CVCL_9C68
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 45,X0 (ECACC=92071701)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9C68 Copy
https://web.expasy.org/cellosaurus/CVCL_9C64
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18 (ECACC=92071008)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9C64 Copy
https://web.expasy.org/cellosaurus/CVCL_9C79
Organism: Homo sapiens (Human)
Disease: Trisomy 8
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+8 (ECACC=920717262)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9C79 Copy
https://web.expasy.org/cellosaurus/CVCL_9C68
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 45,X0 (ECACC=92071701)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92071701, RRID:CVCL_9C68 Copy
https://web.expasy.org/cellosaurus/CVCL_9C59
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18 (ECACC=92070608)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_9C59 Copy
https://web.expasy.org/cellosaurus/CVCL_9C92
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+18 (ECACC=92072902)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92072902, RRID:CVCL_9C92 Copy
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