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    首頁(yè) /科研細胞 /人源細胞系 / /MSTO-211H(人雙向性肺癌細胞)

    MSTO-211H(人雙向性肺癌細胞)

    CBP60109

    產(chǎn)品描述
    產(chǎn)品數據庫
    I. General information 
    Synonyms: MSTO-211H
    Background: The MSTO-211H cell line was established in 1985 from the pleural effusion of a patient with biphasic mesothelioma of the lung.,Derived from metastatic site, lung
    Species: Homo sapiens, human
    Tissue: lung; derived from metastatic site: pleural effusion
    Disease: biphasic mesothelioma
    Gender: male,62 years, Caucasian
    Morphology: fibroblast
    Growth Mode: adherent
    Doubling Time: 20 hrs
    DNA Profile: Amelogenin: X,Y
    CSF1PO: 11,12
    D13S317: 11,14
    D16S539: 13
    D5S818: 12
    D7S820: 8,12
    THO1: 8,9.3
    TPOX: 11
    vWA: 16,18
    Our Cell Line Authentication Service
    Culture Medium:

    RPMI-1640+10%FBS

    MSTO-211H完全培養基,#CBP60109M
    We strongly suggest to purchase the complete medium from us.

    Cryopreservation medium: 90%FBS+10%DMSO
    Oncogene: c-myc +; v-src +; v-abl +; v-erb B +; c-raf 1 +; H-ras +; K-ras +; N-ras +; N-myc -; L-myc -; c-myb -; c-fos -; v-fes -; v-fms -; v-sis -
    Tumor Formation: Yes, tumors for med in approximately 20% of nude mice inoculated with MSTO-211H cells
    Comments: The patient had not received prior radiation or chemotherapy. MSTO-211H cells have high affinity binding sites for EGF, and express Neuron specific enolase (NSE) and both the alpha and beta subunits of human chorionic gonadotropin (HCG).
    L-DOPA decarboxylase (DDC), bombesin and neurotensin were not detected.The cells overexpress the c-myc protooncogene, and no gene rearrangement or amplification was observed.They are positive for the expression of v-src, v-abl, v-erb B, c-raf 1, Ha-ras, Ki-ras, and N-ras.Expression of N-myc, L-myc, c-myb, c-fos, v-fes, v-fms and v-sis oncogene expression was not detected.The cells can reach a saturation density of 400000 cells per sq cm, but will slough off of the surface as they attain this density.
    For more information, please contact us (4008-750-250).

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