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.
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https://web.expasy.org/cellosaurus/CVCL_RB62
Organism: Homo sapiens (Human)
Disease: Alzheimer's disease
Category: Induced pluripotent stem cell
Comments: From: StemBANCC; Oxford; United Kingdom.
Proper citation: EBiSC Cat# STBCi016-A, RRID:CVCL_RB62 Copy
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https://web.expasy.org/cellosaurus/CVCL_RB72
Organism: Homo sapiens (Human)
Disease: Parkinson disease 1, autosomal dominant
Category: Induced pluripotent stem cell
Comments: From: StemBANCC; Oxford; United Kingdom.
Proper citation: RRID:CVCL_RB72 Copy
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https://web.expasy.org/cellosaurus/CVCL_RC64
Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: From: StemBANCC; Oxford; United Kingdom.
Proper citation: ECACC Cat# 66540772, RRID:CVCL_RC64 Copy
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https://web.expasy.org/cellosaurus/CVCL_RC64
Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: From: StemBANCC; Oxford; United Kingdom.
Proper citation: EBiSC Cat# STBCi056-A, RRID:CVCL_RC64 Copy
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https://web.expasy.org/cellosaurus/CVCL_Y122
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type IV
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_Y122 Copy
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https://web.expasy.org/cellosaurus/CVCL_Y122
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type IV
Category: Finite cell line
Comments:
Proper citation: ATCC Cat# CRL-1406, RRID:CVCL_Y122 Copy
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https://web.expasy.org/cellosaurus/CVCL_V442
Organism: Homo sapiens (Human)
Disease: Autosomal dominant polycystic kidney disease
Category: Transformed cell line
Comments:
Proper citation: ATCC Cat# CRL-2835, RRID:CVCL_V442 Copy
Contaminated Discontinued
https://web.expasy.org/cellosaurus/CVCL_A342
Organism: Homo sapiens (Human)
Disease: Human papillomavirus-related cervical squamous cell carcinoma
Category: Cancer cell line
Comments: Miscellaneous: STR profile from personal communication of Chow, Kin-Hoe., Population: Caucasian., Problematic cell line: Contaminated. Shown to be a ME-180 derivative (BCRC=60145 and STR profile). Originally thought to originate from a 56 year old male patient with a grade 2 stage A papillary transitional cell carcinoma..
Proper citation: RRID:CVCL_A342 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y80
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90062723, RRID:CVCL_8Y80 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y83
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8Y83 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y87
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8Y87 Copy
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https://web.expasy.org/cellosaurus/CVCL_C318
Organism: Mus musculus (Mouse)
Disease:
Category: Embryonic stem cell
Comments: Part of: ENCODE project mouse cell lines.
Proper citation: RCB Cat# AES0014, RRID:CVCL_C318 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y82
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8Y82 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y86
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8Y86 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y81
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90062724, RRID:CVCL_8Y81 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y94
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91042501, RRID:CVCL_8Y94 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y84
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91012408, RRID:CVCL_8Y84 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y88
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91012414, RRID:CVCL_8Y88 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y86
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91012411, RRID:CVCL_8Y86 Copy
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https://web.expasy.org/cellosaurus/CVCL_8Y97
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Caution: Was removed from the ECACC collection on demand of the person that established that cell line., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8Y97 Copy
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