CAL-62/CAL-62/CAL-62/人甲状腺癌细胞
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CAL-62/CAL-62/CAL-62/人甲状腺癌细胞

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

      CAL-62

    • 库存

      1x10^6/瓶/支

    • 供应商

      上海酶研

    • 肿瘤类型

      详询

    • 细胞类型

      人甲状腺癌细胞

    • ATCC Number

      详询

    • 品系

      CAL-62

    • 组织来源

      人甲状腺癌细胞

    • 相关疾病

      CAL-62

    • 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

      人甲状腺癌细胞

    • 运输方式

      顺丰快递

    • 年限

      5年

    • 生长状态

      生长良好

    CAL-62/CAL-62细胞系/CAL-62细胞株/CAL-62人甲状腺癌细胞

    Cell line name CAL-62

    Synonyms Cal-62; CAL 62; Cal 62; CAL62; Centre Antoine Lacassagne-62

    Accession CVCL_1112

    Resource Identification Initiative To cite this cell line use: CAL-62 (RRID:CVCL_1112)

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

    Part of: COSMIC cell lines project.

    Population: Caucasian.

    Doubling time: ~24 hours (DSMZ=ACC-448).

    Microsatellite instability: Stable (MSS) (Sanger).

    Omics: Deep exome analysis.

    Omics: Deep quantitative proteome analysis.

    Omics: DNA methylation analysis.

    Omics: SNP array analysis.

    Omics: Transcriptome analysis by microarray.

    Omics: Transcriptome analysis by RNAseq.

    Derived from site: In situ; Thyroid gland; UBERON=UBERON_0002046.

    Sequence variations

    Mutation; HGNC; 2348; CREBBP; Simple; p.Glu1541Ter (c.4621G>T); Zygosity=Heterozygous (PubMed=30737244).

    Mutation; HGNC; 3373; EP300; Simple; p.Asp1485fs (c.4454delA); Zygosity=Homozygous (PubMed=30737244).

    Mutation; HGNC; 6407; KRAS; Simple; p.Gly12Arg (c.34G>C); ClinVar=VCV000012579; Zygosity=Homozygous (PubMed=23833040; PubMed=30737244).

    Mutation; HGNC; 7773; NF2; Simple; p.Glu215Ter (c.643G>T); Zygosity=Homozygous (PubMed=30737244).

    Mutation; HGNC; 11998; TP53; Simple; p.Ala161Asp (c.482C>A); ClinVar=VCV000422295; Zygosity=Homozygous (PubMed=30737244).

    Genome ancestry Source: PubMed=30894373

     

    Origin % genome

    African 0.55

    Native American 0.27

    East Asian, North 1.91

    East Asian, South 0

    South Asian 1.04

    European, North 46.22

    European, South 50.02

    Disease Thyroid gland anaplastic carcinoma (NCIt: C3878)

    Anaplastic thyroid carcinoma (ORDO: Orphanet_142)

    Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)

    Sex of cell Female

    Age at sampling 70Y

    Category Cancer cell line

    STR profile Source(s): Cosmic-CLP=906828; DSMZ=ACC-448; PubMed=18713817; PubMed=25365311; PubMed=30737244

     

    Markers:

    Amelogenin X

    CSF1PO 9,12

    D2S1338 19,23

    D3S1358 16

    D5S818 9,12

    D7S820 10

    D8S1179 13

    D13S317 12

    D16S539 12,13

    D18S51 16

    D19S433 14

    D21S11 32.2

    FGA 19

    Penta D 13

    Penta E 5,10

    TH01 7,9

    TPOX 8,9

    vWA 16

     

    Run an STR similarity search on this cell line

    Publications

    PubMed=1369551

    Gioanni J., Zanghellini E., Mazeau C., Zhang D., Courdi A., Farges M.-F., Lambert J.-C., Duplay H., Schneider M.

    Characterization of a human cell line from an anaplastic carcinoma of the thyroid gland.

    Bull. Cancer 78:1053-1062(1991)

     

    PubMed=18713817; DOI=10.1210/jc.2008-1102; PMCID=PMC2582569

    Schweppe R.E., Klopper J.P., Korch C.T., Pugazhenthi U., Benezra M., Knauf J.A., Fagin J.A., Marlow L.A., Copland J.A. 3rd, Smallridge R.C., Haugen B.R.

    Deoxyribonucleic acid profiling analysis of 40 human thyroid cancer cell lines reveals cross-contamination resulting in cell line redundancy and misidentification.

    J. Clin. Endocrinol. Metab. 93:4331-4341(2008)

     

    PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113

    Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.

    Signatures of mutation and selection in the cancer genome.

    Nature 463:893-898(2010)

     

    PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662

    Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.

    A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.

    Cancer Res. 70:2158-2164(2010)

     

    PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027

    Barretina J.G., Caponigro G., Stransky N., Venkatesan K., Margolin A.A., Kim S., Wilson C.J., Lehar J., Kryukov G.V., Sonkin D., Reddy A., Liu M., Murray L., Berger M.F., Monahan J.E., Morais P., Meltzer J., Korejwa A., Jane-Valbuena J., Mapa F.A., Thibault J., Bric-Furlong E., Raman P., Shipway A., Engels I.H., Cheng J., Yu G.-Y.K., Yu J.-J., Aspesi P. Jr., de Silva M., Jagtap K., Jones M.D., Wang L., Hatton C., Palescandolo E., Gupta S., Mahan S., Sougnez C., Onofrio R.C., Liefeld T., MacConaill L.E., Winckler W., Reich M., Li N.-X., Mesirov J.P., Gabriel S.B., Getz G., Ardlie K., Chan V., Myer V.E., Weber B.L., Porter J., Warmuth M., Finan P., Harris J.L., Meyerson M.L., Golub T.R., Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.

    The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.

    Nature 483:603-607(2012)

     

    PubMed=23833040; DOI=10.1210/jc.2013-2383; PMCID=PMC3763971

    Landa I., Ganly I., Chan T.A., Mitsutake N., Matsuse M., Ibrahimpasic T., Ghossein R.A., Fagin J.A.

    Frequent somatic TERT promoter mutations in thyroid cancer: higher prevalence in advanced forms of the disease.

    J. Clin. Endocrinol. Metab. 98:E1562-E1566(2013)

     

    PubMed=25365311; DOI=10.1210/jc.2014-2359; PMCID=PMC4318896

    Garg M., Okamoto R., Nagata Y., Kanojia D., Venkatesan S., Anand M.T., Braunstein G.D., Said J.W., Doan N.B., Ho Q., Akagi T., Gery S., Liu L.-Z., Tan K.T., Chang W.J., Yang H.H., Ogawa S., Koeffler H.P.

    Establishment and characterization of novel human primary and metastatic anaplastic thyroid cancer cell lines and their genomic evolution over a year as a primagraft.

    J. Clin. Endocrinol. Metab. 100:725-735(2015)

     

    PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469

    Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., M, Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.

    A landscape of pharmacogenomic interactions in cancer.

    Cell 166:740-754(2016)

     

    PubMed=30737244; DOI=10.1158/1078-0432.CCR-18-2953; PMCID=PMC6522280

    Landa I., Pozdeyev N., Korch C.T., Marlow L.A., Smallridge R.C., Copland J.A. 3rd, Henderson Y.C., Lai S.Y., Clayman G.L., Onoda N., Tan A.-C., Garcia-Rendueles M.E.R., Knauf J.A., Haugen B.R., Fagin J.A., Schweppe R.E.

    Comprehensive genetic characterization of human thyroid cancer cell lines: a validated panel for preclinical studies.

    Clin. Cancer Res. 25:3141-3151(2019)

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