P3X63Ag8

P3X63Ag8

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  • 2025年12月02日
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    • 详细信息
    • 技术资料
    • 运输方式

      冻存运输

    • 品系

      BALB/c

    • 物种来源

      小鼠

    • 是否是肿瘤细胞

      0

    • 细胞类型

      B淋巴细胞

    • 免疫类型

      IgG1; kappa light chain

    • 细胞形态

      淋巴样

    • 相关疾病

      多发性骨髓瘤

    • ATCC Number

      TIB-9™

    • 生长状态

      悬浮生长

    • 库存

      大量

    Designations: P3X63Ag8
    Depositors:  G Kohler, C Milstein
    Isotype: IgG1; kappa light chain
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: suspension
    Organism: Mus musculus
    Morphology: lymphoblast

    Source: Disease: plasmacytoma; myeloma
    Strain: BALB/c
    Cell Type: B lymphocyte;
    Cellular Products: immunoglobulin; monoclonal antibody
    Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
    Antigen Expression: H-2d
    Cytogenetic Analysis: hyperdiploid; modal number = 65
    Comments: This line was derived from the P3K cell line (a tissue culture line established from the MOPC-21 plasmacytoma).
    The line is resistant to 0.1 mM 8-azaguanine and die in HAT medium.
    The cells have been reported to be cholesterol auxotrophs due to a deficiency in 3-ketosteroid reductase activity.
    Tested and found negative for ectromelia virus (mousepox).
    Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
    Subculturing: Medium Renewal: Every 2 to 3 days
    Cultures can be maintained by addition or replacement of fresh medium. Start cultures at 2 X 10 exp5 cells/ml and maintain between 1 X 10 exp5 and 1 X 10 exp6 cells/ml.
    References: 1042: Koprowski H, et al. Production of antibodies against influenza virus by somatic cell hybrids between mouse myeloma and primed spleen cells. Proc. Natl. Acad. Sci. USA 74: 2985-2988, 1977. PubMed: 268647
    1112: Kohler G, Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature 256: 495-497, 1975. PubMed: 1172191
    22154: Horibata K, Harris AW. Mouse myelomas and lymphomas in culture. Exp. Cell Res. 60: 61-77, 1970. PubMed: 5439579
    22173: Kohler G, et al. Fusion of T and B cells. Somatic Cell Genet. 3: 303-312, 1977. PubMed: 305123
    22347: Kohler G, Milstein C. Derivation of specific antibody-producing tissue culture and tumor lines by cell fusion. Eur. J. Immunol. 6: 511-519, 1976. PubMed: 825377
    23366: Sato JD, et al. Effects of proximate cholesterol precursors and steroid hormones on mouse myeloma growth in serum-free medium. In Vitro Cell. Dev. Biol. 24: 1223-1228, 1988. PubMed: 3209588
    26333: Ramasamy R, et al. Possible role for the Fc receptor on B lymphocytes. Nature 249: 573-574, 1974. PubMed: 4545851
    26334: Lemke H, et al. Hybrid cell lines secreting monoclonal antibody specific for major histocompatibility antigens of the mouse. Nature 271: 249-251, 1978. PubMed: 74805
    26335: . . Eur. J. Immunol. 3: 135-140, 1973.
    26336: Secher DS, et al. Spontaneous mutation in tissue culture-chemical nature of variant immunoglobulin from mutant clones of MOPC 21. FEBS Lett. 37: 311-316, 1973. PubMed: 4763339

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