• mgm4858am集团

    mgm4858am集团 /科研细胞 /人源细胞系 /血液 /NK92MI(人恶性非霍奇金淋巴瘤患者的自然杀伤细胞)

    NK92MI(人恶性非霍奇金淋巴瘤患者的自然杀伤细胞)

    CBP61113

    询 价
    NK92MI细胞全景
    产品描述
    产品数据库
    I. General information 
    Synonyms: NK92MI
    Background: NK-92MI is an interleukin-2 (IL-2) independent Natural Killer Cell line derived from the NK-92 (ATCC CRL-2407) cell line by transfection. NK-92 is an interleukin-2 (IL-2) dependent Natural Killer Cell line derived from peripheral blood mononuclear cells from a 50 year old Caucasian male with rapidly progressive non-Hodgkin's lymphoma. The parental cells were transfected with human IL-2 cDNA in the retroviral MFG-hIL-2 vector by particle-mediated gene transfer. The transfection is stable.
    Species: Homo sapiens, human
    Tissue: peripheral blood, blood
    Disease: malignant non-Hodgkin's lymphoma
    Gender: male, 50 years,  Caucasian
    Morphology: lymphoblast
    Growth Mode: suspension, multicell aggregates
    Doubling Time: N/A
    DNA Profile: D5S818: 12. 13
    D13S317: 9, 12
    D7S820: 10, 11
    D16S539: 11, 12
    vWA: 16, 18
    THO1: 6, 9.3
    TPOX: 8
    CSF1PO: 11, 12
    Amelogenin: X, Y
    Our Cell Line Authentication Service
    Culture Medium:

    75%  MEM α (GIBCO 12561-056 )  + 12.5% FBS+12.5% horse serum + 0.2 mM inositoll+0.02 mM folic acid+0.05 mM  2-mercaptoethanol

    NK92MI完全培养基,# CBP61113M
    We strongly suggest to purchase the complete medium from us.

    Cryopreservation medium: 90%FBS+10%DMSO
    Antigen Expression: N/A
    Receptor Expression: N/A
    Oncogene: N/A
    Genes Expressed: N/A
    Cellular Products: N/A
    Tumor Formation: N/A
    Comments:  
    NK-92 and this derivative cell line NK-92MI have the following characteristics: surface marker positive for CD2, CD7, CD11a, CD28, CD45, CD54 and CD56 bright; surface marker negative for CD1, CD3, CD4, CD5, CD8, CD10, CD14, CD16, CD19, CD20, CD23, CD34 and HLA-DR.
    The parental IL-2 dependent cell line is available as ATCC CRL-2407 (NK-92). NK-92MI was shown to contain, express, and synthesize the hIL-2.
    A culture submitted to the ATCC in September of 1998 was found to be contaminated with mycoplasma. Progeny were cured by a 21-day treatment with BM Cycline. The cells were assayed for mycoplasma, by the Hoechst stain, PCR and the standard culture test, after a six-week period following treatment. All tests were negative.
    ATCC confirmed this cell line is positive for the presence of Epstein-Barr viral DNA sequences via PCR.
    For more information, please contact us (4008-750-250).

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