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        產(chǎn)品詳情
        • 產(chǎn)品名稱:小鼠血液細(xì)胞

        • 產(chǎn)品型號:TIB-68
        • 產(chǎn)品廠商:美國標(biāo)準(zhǔn)生物品收藏中心(ATCC)
        • 產(chǎn)品價格:0
        • 折扣價格:0
        • 產(chǎn)品文檔:
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        簡單介紹:
        TIB-68 WEHI-3 小鼠血液細(xì)胞,原代細(xì)胞、細(xì)胞系。細(xì)胞庫管理規(guī)范,提供的細(xì)胞株背景清楚,提供參考文獻(xiàn)和培養(yǎng)條件,
        詳情介紹:
        TIB-68 WEHI-3 小鼠血液細(xì)胞
        ATCC® Number: TIB-68?    Price: $303.00
        Designations: WEHI-3
        Depositors:  M Cohn
        Biosafety Level: 1
        Shipped: frozen
        Medium & Serum: See Propagation
        Growth Properties: suspension (some adherent cells)
        Organism: Mus musculus (mouse)
        Morphology:
        Source: Organ: peripheral blood
        Strain: BALB/c
        Disease: leukemia
        Cellular Products: lysozyme; granulocyte colony stimulating activity (CSA); interleukin-3 (interleukin 3, IL-3)
        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.
         
        Receptors: complement (C3)
        Comments: The growth of WEHI-3 is inhibited by 4 ng/ml LPS and blocked by higher concentrations.
        Dextran sulfate at 30 to 40 mcg/ml also inhibits growth.
        Latex beads are phagocytized but are not toxic.
        Zymosan and BCG are phagocytized and block growth.
        The cells exhibit only weak effector activity in antibody dependent cell mediated cytotoxicity.
        Tested and found negative for ectromelia virus (mousepox).
        Propagation: ATCC complete growth medium: Iscove's modified Dulbecco's medium with 4 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate and supplemented with 0.05 mM 2-mercaptoethanol, 90%; fetal bovine serum, 10%
        Temperature: 37.0°C
        Subculturing: Medium Renewal: Every 2 to 3 days
        Cultures can be maintained by the addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation with subsequent resuspension at 2 X 10 exp5 viable cells/ml.
        Maintain cell density between 2 X 10 exp5 and 2 X 10 exp6 viable cells/ml.
        Adherent cells may be harvested by scraping.
        Preservation: culture medium 95%; DMSO, 5%
        Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2005
        recommended serum:ATCC 30-2020
        References: 1080: Ralph P, et al. Lysozyme synthesis by established human and murine histiocytic lymphoma cell lines. J. Exp. Med. 143: 1528-1533, 1976. PubMed: 1083890
        1135: Ralph P, Nakoinz I. Antibody-dependent killing of erythrocyte and tumor targets by macrophage-related cell lines: enhancement by PPD and LPS. J. Immunol. 119: 950-954, 1977. PubMed: 894031
        1136: Ralph P, Nakoinz I. Direct toxic effects of immunopotentiators on monocytic myelomonocytic, and histiocytic or macrophage tumor cells in culture. Cancer Res. 37: 546-550, 1977. PubMed: 318922
        23431: McKean DJ, et al. Major histocompatibility complex-restricted antigen presentation to antigen-reactive T cells by B lymphocyte tumor cells. J. Exp. Med. 154: 1419-1431, 1981. PubMed: 6170720
        33035: Boring L, et al. Molecular cloning and functional expression of murine JE (monocyte chemoattractant protein 1) and murine macrophage inflammatory protein 1alpha receptors. J. Biol. Chem. 271: 7551-7558, 1996. PubMed: 8631787
         
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