SW480/SW480/SW480/人结肠腺癌细胞
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SW480/SW480/SW480/人结肠腺癌细胞

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    • 详细信息
    • 文献和实验
    • 技术资料
    • 英文名

      SW480

    • 库存

      1x10^6/瓶/支

    • 供应商

      上海酶研

    • 肿瘤类型

    • 细胞类型

      人结肠腺癌细胞

    • ATCC Number

      详询

    • 品系

      SW480

    • 组织来源

      人结肠腺癌细胞

    • 相关疾病

      SW480

    • 物种来源

      哺乳动物

    • 免疫类型

      详询

    • 细胞形态

      贴壁/悬浮

    • 是否是肿瘤细胞

      详询

    • 器官来源

      人结肠腺癌细胞

    • 运输方式

      顺丰快递

    • 年限

      5年

    • 生长状态

      生长良好

    SW480/SW480细胞系/SW480细胞株/SW480人结肠腺癌细胞

    Cell line name SW480

    Synonyms SW-480; SW 480; SW480E

    Accession CVCL_0546

    Resource Identification Initiative To cite this cell line use: SW480 (RRID:CVCL_0546)

    Comments Part of: AstraZeneca Colorectal cell line (AZCL) panel.

    Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).

    Part of: KuDOS 95 cell line panel.

    Part of: MD Anderson Cell Lines Project.

    From: Scott and White Clinic; Temple; USA.

    Population: Caucasian.

    Doubling time: 50 hours (Note=At 73th passage) (PubMed=1000501); 30.74 hours (PubMed=25944804); 24 hours (PubMed=25984343); 20-25 hours (CLS=300302); ~25-30 hours (DSMZ=ACC-313); ~38 hours (PBCF).

    Microsatellite instability: Stable (MSS) (PubMed=9000147; PubMed=10674020; PubMed=24042735; PubMed=24755471; PubMed=25926053; PubMed=28683746).

    Omics: Deep exome analysis.

    Omics: Deep phosphoproteome analysis.

    Omics: Deep proteome analysis.

    Omics: Deep quantitative proteome analysis.

    Omics: DNA methylation analysis.

    Omics: Hi-C chromosome conformation analysis.

    Omics: miRNA expression profiling.

    Omics: N-glycan profiling.

    Omics: Nuclear proteome analysis.

    Omics: O-glycan profiling.

    Omics: Protein expression by reverse-phase protein arrays.

    Omics: shRNA library screening.

    Omics: SNP array analysis.

    Omics: Transcriptome analysis by microarray.

    Omics: Transcriptome analysis by RNAseq.

    Misspelling: WE-480; Note=Occasionally.

    Misspelling: WE480; Note=Occasionally.

    Misspelling: SW80; Note=Occasionally.

    Misspelling: SWH80; BTO=BTO:0006552.

    Derived from site: In situ; Colon; UBERON=UBERON_0001155.

    PubMed=7651727

    Kastrinakis W.V., Ramchurren N., Rieger K.M., Hess D.T., Loda M., Steele G., Summerhayes I.C.

    Increased incidence of p53 mutations is associated with hepatic metastasis in colorectal neoplastic progression.

    Oncogene 11:647-652(1995)

     

    PubMed=7824277

    Eshleman J.R., Lang E.Z., Bowerfind G.K., Parsons R., Vogelstein B., Willson J.K.V., Veigl M.L., Sedwick W.D., Markowitz S.D.

    Increased mutation rate at the hprt locus accompanies microsatellite instability in colon cancer.

    Oncogene 10:33-37(1995)

     

    PubMed=8895552; DOI=10.1002/(SICI)1097-0215(19960927)68:1<126::AID-IJC22>3.0.CO;2-8

    Suardet L., Li C., Little J.B.

    Radio-induced modulation of transforming growth factor beta1 sensitivity in a p53 wild-type human colorectal-cancer cell line.

    Int. J. Cancer 68:126-131(1996)

     

    PubMed=9000147

    Cottu P.-H., Muzeau F., Estreicher A., Flejou J.-F., Iggo R.D., Thomas G., Hamelin R.

    Inverse correlation between RER+ status and p53 mutation in colorectal cancer cell lines.

    Oncogene 13:2727-2730(1996)

     

    PubMed=9000572

    Hoang J.-M., Cottu P.-H., Thuille B., Salmon R.J., Thomas G., Hamelin R.

    BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines.

    Cancer Res. 57:300-303(1997)

     

    PubMed=9290701; DOI=10.1002/(SICI)1098-2744(199708)19:4<243::AID-MC5>3.0.CO;2-D

    Jia L.-Q., Osada M., Ishioka C., Gamo M., Ikawa S., Suzuki T., Shimodaira H., Niitani T., Kudo T., Akiyama M., Kimura N., Matsuo M., Mizusawa H., Tanaka N., Koyama H., Namba M., Kanamaru R., Kuroki T.

    Screening the p53 status of human cell lines using a yeast functional assay.

    Mol. Carcinog. 19:243-253(1997)

     

    PubMed=9294210; DOI=10.1073/pnas.94.19.10330; PMCID=PMC23362

    Ilyas M., Tomlinson I.P.M., Rowan A.J., Pignatelli M., Bodmer W.F.

    Beta-catenin mutations in cell lines established from human colorectal cancers.

    Proc. Natl. Acad. Sci. U.S.A. 94:10330-10334(1997)

     

    PubMed=9715273; DOI=10.1038/sj.onc.1201986

    Eshleman J.R., Casey G., Kochera M.E., Sedwick W.D., Swinler S.E., Veigl M.L., Willson J.K.V., Schwartz S., Markowitz S.D.

    Chromosome number and structure both are markedly stable in RER colorectal cancers and are not destabilized by mutation of p53.

    Oncogene 17:719-725(1998)

     

    PubMed=10674020; DOI=10.1016/S0959-8049(99)00206-3

    Ku J.-L., Yoon K.-A., Kim D.-Y., Park J.-G.

    Mutations in hMSH6 alone are not sufficient to cause the microsatellite instability in colorectal cancer cell lines.

    Eur. J. Cancer 35:1724-1729(1999)

     

    PubMed=10612807; DOI=10.1002/(SICI)1098-2264(200002)27:2<183::AID-GCC10>3.0.CO;2-P; PMCID=PMC4721570

    Ghadimi B.M., Sackett D.L., Difilippantonio M.J., Schrock E., Neumann T., Jauho A., Auer G., Ried T.

    Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations.

    Genes Chromosomes Cancer 27:183-190(2000)

     

    PubMed=10737795; DOI=10.1073/pnas.97.7.3352; PMCID=PMC16243

    Rowan A.J., Lamlum H., Ilyas M., Wheeler J., Straub J., Papadopoulou A., Bicknell D.C., Bodmer W.F., Tomlinson I.P.M.

    APC mutations in sporadic colorectal tumors: a mutational 'hotspot' and interdependence of the 'two hits'.

    Proc. Natl. Acad. Sci. U.S.A. 97:3352-3357(2000)

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    *发表【中文论文】请标注:由上海酶研生物科技有限公司提供;

    *发表【英文论文】请标注:From Shanghai EK-Bioscience Biotechnology Co., Ltd.

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