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_8U26
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 89030312, RRID:CVCL_8U26 Copy
https://web.expasy.org/cellosaurus/CVCL_8U40
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90080203, RRID:CVCL_8U40 Copy
https://web.expasy.org/cellosaurus/CVCL_8U36
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90051418, RRID:CVCL_8U36 Copy
https://web.expasy.org/cellosaurus/CVCL_E553
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel.
Proper citation: ECACC Cat# 94082289, RRID:CVCL_E553 Copy
https://web.expasy.org/cellosaurus/CVCL_8U38
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90060802, RRID:CVCL_8U38 Copy
https://web.expasy.org/cellosaurus/CVCL_AQ55
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90100305, RRID:CVCL_AQ55 Copy
https://web.expasy.org/cellosaurus/CVCL_8U70
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 88122801, RRID:CVCL_8U70 Copy
https://web.expasy.org/cellosaurus/CVCL_8U56
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;8)(q13.1;p11) (ECACC=90081712)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90081712, RRID:CVCL_8U56 Copy
https://web.expasy.org/cellosaurus/CVCL_8U49
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90101607, RRID:CVCL_8U49 Copy
https://web.expasy.org/cellosaurus/CVCL_8U85
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91011606, RRID:CVCL_8U85 Copy
https://web.expasy.org/cellosaurus/CVCL_8U45
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90092709, RRID:CVCL_8U45 Copy
https://web.expasy.org/cellosaurus/CVCL_AQ56
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90101601, RRID:CVCL_AQ56 Copy
https://web.expasy.org/cellosaurus/CVCL_8U64
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 89120582, RRID:CVCL_8U64 Copy
https://web.expasy.org/cellosaurus/CVCL_8U44
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90092708, RRID:CVCL_8U44 Copy
https://web.expasy.org/cellosaurus/CVCL_8U54
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90091103, RRID:CVCL_8U54 Copy
https://web.expasy.org/cellosaurus/CVCL_8U62
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90011204, RRID:CVCL_8U62 Copy
https://web.expasy.org/cellosaurus/CVCL_8U61
Organism: Homo sapiens (Human)
Disease: Pallister-Killian syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY; 47,XY,+i(12p) (ECACC=90020901)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90020901, RRID:CVCL_8U61 Copy
https://web.expasy.org/cellosaurus/CVCL_8U76
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90121814, RRID:CVCL_8U76 Copy
https://web.expasy.org/cellosaurus/CVCL_8U65
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,-4,+der(4)t(X;4)(p22.1;p15.2); de novo (ECACC=89082301)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 89082301, RRID:CVCL_8U65 Copy
https://web.expasy.org/cellosaurus/CVCL_8U67
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;9)(p21.2;q22.1); de novo (ECACC=89060701)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 89060701, RRID:CVCL_8U67 Copy
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