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on page 1 showing 10 out of 484 results
https://web.expasy.org/cellosaurus/CVCL_VL12

Cite this: (CLS Cat# 300676/p19844_HK-2xZFN-mEGFP-Nup107, RRID:CVCL_VL12)
Organism: Homo sapiens
Disease: Human papillomavirus-related endocervical adenocarcinoma
Category: Cancer cell line
Comment: Characteristics: Edited by ZFN at the NUP107 locus to insert a mEGFP construct at the N-terminus of both allele of the gene. Transfected with: UniProtKB; P42212; GFP (with p.Phe64Leu, p.Ser65Thr and p.His231Leu = EGFP). Transformant: NCBI_TaxID; 333761; Human papillomavirus type 18 (HPV18).

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https://web.expasy.org/cellosaurus/CVCL_VL13

Cite this: (CLS Cat# 300173/p21702_HK-ZFN-AURKB-mEGFP, RRID:CVCL_VL13)
Organism: Homo sapiens
Disease: Human papillomavirus-related endocervical adenocarcinoma
Category: Cancer cell line
Comment: Characteristics: Edited by ZFN at the AURKB locus to insert a mEGFP construct at the N-terminus of the gene. Transfected with: UniProtKB; P42212; GFP (with p.Phe64Leu, p.Ser65Thr and p.His231Leu = EGFP). Transformant: NCBI_TaxID; 333761; Human papillomavirus type 18 (HPV18).

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https://web.expasy.org/cellosaurus/CVCL_VL14

Cite this: (CLS Cat# 300270/p22470_HK-ZFN-AURKB-mEGFP,_ZFN-INCEMP-mCherry, RRID:CVCL_VL14)
Organism: Homo sapiens
Disease: Human papillomavirus-related endocervical adenocarcinoma
Category: Cancer cell line
Comment: Characteristics: Edited by ZFN at the AURKB locus to insert a mEGFP construct at the N-terminus of both alleles of the gene and at the INCENP locus to insert a mCherry construct at the N-terminus of one allele of the gene. Transfected with: UniProtKB; P42212; GFP (with p.Phe64Leu, p.Ser65Thr and p.His231Leu = EGFP). Transfected with: UniProtKB; X5DSL3; mCherry fluorescent protein. Transformant: NCBI_TaxID; 333761; Human papillomavirus type 18 (HPV18). Misspelling: HK-ZFN-AURKB-mEGFP, ZFN-INCEMP-mCherry; In CLS entry until July 2018.

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https://web.expasy.org/cellosaurus/CVCL_X910

Cite this: (CLS Cat# 300118/p803_NCH421K, RRID:CVCL_X910)
Organism: Homo sapiens
Disease: Glioblastoma
Category: Cancer cell line
Comment:

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https://web.expasy.org/cellosaurus/CVCL_0002

Cite this: (CLS Cat# 300209/p671_HL-60, RRID:CVCL_0002)
Organism: Homo sapiens
Disease: Adult acute myeloid leukemia
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: COSMIC cell lines project. Part of: ENCODE project common cell types; tier 3. Part of: MD Anderson Cell Lines Project. Part of: MYC genetic alteration cell panel (ATCC TCP-1035). Registration: National Institute of Standards and Technology, Standard Reference Materials; SRM 2392-I. Biotechnology: Used a source of mitochondrial DNA for USA forensic testing. Doubling time: 28 hours (PubMed=25984343); ~40 hours (DSMZ). Microsatellite instability: Stable (MSS) (PubMed=12661003; Sanger). Sequence variation: Homozygous for CDKN2A p.Arg80Ter (c.238C>T) (PubMed=17088437). Sequence variation: Heterozygous for NRAS p.Gln61Leu (c.182A>T) (PubMed=17088437). Omics: Array-based CGH. Omics: Cell surface proteome. Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: H3K4me3 ChIP-seq epigenome analysis. Omics: Mitochondrial genome sequenced. Omics: N-glycan profiling. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Misspelling: IIL-60; Occasionally. Discontinued: JCRB; NIHS0086. Derived from sampling site: Peripheral blood.

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https://web.expasy.org/cellosaurus/CVCL_0004

Cite this: (CLS Cat# 300224/p473_K-562, RRID:CVCL_0004)
Organism: Homo sapiens
Disease: Chronic myelogenous leukemia, BCR-ABL1 positive
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: COSMIC cell lines project. Part of: ENCODE project common cell types; tier 1. Part of: MD Anderson Cell Lines Project. Part of: NCI-60 cancer cell line panel. Doubling time: 47 hours (PubMed=25984343); 19.6 hours (NCI-DTP); ~30-40 hours (DSMZ). HLA typing: A*11:01:01,31:01:02; B*18,40; C*03; DPB1*04:01,04:02; DQB1*02:01,03:02; DRB1*03,04 (PubMed=15748285). HLA typing: A*11; B*40,35/39; C*05,03 (PubMed=25960936). Microsatellite instability: Stable (MSS) (PubMed=23671654; Sanger). Sequence variation: Homozygous for TP53 p.Gln136fs*13 (c.406_407insC) (PubMed=17088437; PubMed=18277095). Omics: Array-based CGH. Omics: CNV analysis. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Fluorescence phenotype profiling. Omics: Genome sequenced. Omics: H3K27ac ChIP-seq epigenome analysis. Omics: H3K27me3 ChIP-seq epigenome analysis. Omics: H3K36me3 ChIP-seq epigenome analysis. Omics: H3K4me1 ChIP-seq epigenome analysis. Omics: H3K4me2 ChIP-seq epigenome analysis. Omics: H3K4me3 ChIP-seq epigenome analysis. Omics: H3K79me2 ChIP-seq epigenome analysis. Omics: H3K9ac ChIP-seq epigenome analysis. Omics: H3K9me1 ChIP-seq epigenome analysis. Omics: H3K9me3 ChIP-seq epigenome analysis. Omics: H4K20me1 ChIP-seq epigenome analysis. Omics: lncRNA expression profiling. Omics: Metabolome analysis. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Omics: Virome analysis using proteomics. Misspelling: K-652; In Cosmic 1523829. Misspelling: K652; In Cosmic 1516632 and Cosmic 2024372. Derived from sampling site: Pleural effusion.

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https://web.expasy.org/cellosaurus/CVCL_0006

Cite this: (CLS Cat# 300356/p804_THP-1, RRID:CVCL_0006)
Organism: Homo sapiens
Disease: Childhood acute monocytic leukemia
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: COSMIC cell lines project. Part of: MD Anderson Cell Lines Project. Part of: RAS genetic alteration cell panel (ATCC TCP-1031). Part of: Tumor Immunology Bank (TIB) collection from Salk (transferred to ATCC in 1981). Characteristics: Can differentiate from monocytes into macrophage-like cells upon stimulation with PMA. Doubling time: 60-70 hours (PubMed=6970727); 26 hours (PubMed=25984343); ~35-50 hours (DSMZ). HLA typing: A*02; B*15:11; C*03; DQB1*05,06; DRB1*01,15; DRB5*01/02 (PubMed=22674354). Microsatellite instability: Stable (MSS) (Sanger). Sequence variation: Heterozygous for NRAS p.Gly12Asp (c.35G>A) (ATCC); p.Gly12Ser according to PubMed=9379676. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep promoter analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Glycoproteome analysis by proteomics. Omics: Protein expression by reverse-phase protein arrays. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Derived from sampling site: Peripheral blood.

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https://web.expasy.org/cellosaurus/CVCL_0005

Cite this: (CLS Cat# 300299/p638_NB-4, RRID:CVCL_0005)
Organism: Homo sapiens
Disease: Acute promyelocytic leukemia with t(15
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: COSMIC cell lines project. Part of: ENCODE project common cell types; tier 3. Registration: International Depositary Authority, Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ); ACC-2030. Registration: International Depositary Authority, Pasteur Institute Collection Nationale de Cultures de Micro-organismes (CNCM); I-1045. Doubling time: 36-40 hours (PubMed=1995093); 30 hours (PubMed=25984343); ~35-45 hours (DSMZ). Microsatellite instability: Stable (MSS) (Sanger). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: H3K4me3 ChIP-seq epigenome analysis. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Derived from sampling site: Bone marrow.

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https://web.expasy.org/cellosaurus/CVCL_0005

Cite this: (CLS Cat# 300299-SF/p11500_NB-4, RRID:CVCL_0005)
Organism: Homo sapiens
Disease: Acute promyelocytic leukemia with t(15
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: COSMIC cell lines project. Part of: ENCODE project common cell types; tier 3. Registration: International Depositary Authority, Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ); ACC-2030. Registration: International Depositary Authority, Pasteur Institute Collection Nationale de Cultures de Micro-organismes (CNCM); I-1045. Doubling time: 36-40 hours (PubMed=1995093); 30 hours (PubMed=25984343); ~35-45 hours (DSMZ). Microsatellite instability: Stable (MSS) (Sanger). Omics: Cell surface proteome. Omics: Deep antibody staining analysis. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: H3K4me3 ChIP-seq epigenome analysis. Omics: shRNA library screening. Omics: SNP array analysis. Omics: Transcriptome analysis. Derived from sampling site: Bone marrow.

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https://web.expasy.org/cellosaurus/CVCL_0007

Cite this: (CLS Cat# 300368/p474_U-937, RRID:CVCL_0007)
Organism: Homo sapiens
Disease: Adult acute monocytic leukemia
Category: Cancer cell line
Comment: Part of: Cancer Cell Line Encyclopedia (CCLE) project. Characteristics: Can be induced to differentiate into macrophages by several factors such as phorbol ester (PMA) and 12-O-tetradecanoyl-13-phorbol acetate (TPA). Doubling time: 95-100 hours (PubMed=178611); ~30-40 hours (DSMZ). Sequence variation: Hemizygous for PTEN p.Gly129fs*51 (c.387_388insCGCC) (PubMed=10966170). Omics: Deep antibody staining analysis. Omics: Deep proteome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: Proteome analysis by 2D-DE/MS. Omics: SNP array analysis. Omics: Transcriptome analysis. Discontinued: ATCC; CRL-1593. Discontinued: RCB; RCB1978. Discontinued: TKG; TKG 0279. Derived from sampling site: Pleural effusion.

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