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_9G24
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93093021, RRID:CVCL_9G24 Copy
https://web.expasy.org/cellosaurus/CVCL_9G00
Organism: Homo sapiens (Human)
Disease: Klinefelter syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,Y,inv(X)(?q11;q21.2)mat (ECACC=93090203)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93090203, RRID:CVCL_9G00 Copy
https://web.expasy.org/cellosaurus/CVCL_9G07
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93091009, RRID:CVCL_9G07 Copy
https://web.expasy.org/cellosaurus/CVCL_9G09
Organism: Homo sapiens (Human)
Disease: Congenital hydrocephalus
Category: Finite cell line
Comments: Karyotypic information: 46,XY [15]; 47,XY,+20 [5] (ECACC=93091019)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93091019, RRID:CVCL_9G09 Copy
https://web.expasy.org/cellosaurus/CVCL_9G76
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93112927, RRID:CVCL_9G76 Copy
https://web.expasy.org/cellosaurus/CVCL_9G50
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93110302, RRID:CVCL_9G50 Copy
https://web.expasy.org/cellosaurus/CVCL_9G66
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93111504, RRID:CVCL_9G66 Copy
https://web.expasy.org/cellosaurus/CVCL_9G47
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 47,XY,+mar(13/21)mat (ECACC=93103002)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93103002, RRID:CVCL_9G47 Copy
https://web.expasy.org/cellosaurus/CVCL_AQ80
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93112610, RRID:CVCL_AQ80 Copy
https://web.expasy.org/cellosaurus/CVCL_AQ77
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93111807, RRID:CVCL_AQ77 Copy
https://web.expasy.org/cellosaurus/CVCL_9G69
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93111921, RRID:CVCL_9G69 Copy
https://web.expasy.org/cellosaurus/CVCL_9G58
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93110416, RRID:CVCL_9G58 Copy
https://web.expasy.org/cellosaurus/CVCL_AQ78
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93111808, RRID:CVCL_AQ78 Copy
https://web.expasy.org/cellosaurus/CVCL_9G78
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+18 (ECACC=93113001)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93113001, RRID:CVCL_9G78 Copy
https://web.expasy.org/cellosaurus/CVCL_9G41
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93102502, RRID:CVCL_9G41 Copy
https://web.expasy.org/cellosaurus/CVCL_9G65
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93111205, RRID:CVCL_9G65 Copy
https://web.expasy.org/cellosaurus/CVCL_9G43
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93102802, RRID:CVCL_9G43 Copy
https://web.expasy.org/cellosaurus/CVCL_AQ81
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93112611, RRID:CVCL_AQ81 Copy
https://web.expasy.org/cellosaurus/CVCL_9G59
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93110417, RRID:CVCL_9G59 Copy
https://web.expasy.org/cellosaurus/CVCL_9G57
Organism: Homo sapiens (Human)
Disease: Rubinstein-Taybi syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 93119415, RRID:CVCL_9G57 Copy
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