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| 产品名称： | M3/38.1.2.8 HL.2 |
|---|---|
| 商品货号： | TS211558 |
| Organism： | Rattus norvegicus (B cell); Mus musculus (myeloma), rat (B cell); mouse (myeloma) |
| Tissue： | spleen |
| Cell Type： | hybridoma: B lymphocyte |
| Product Format： | frozen |
| Morphology： | lymphoblast |
| Culture Properties： | suspension |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Applications： | Mac-2 and Mac-3 are present on 69% of macrophages and 0% to 2% of thymocytes. Tested and found negative for ectromelia virus (mousepox). |
| Storage Conditions： | liquid nitrogen vapor phase |
| Derivation： | Spleen cells were fused with NS-1 myeloma cells. |
| Genes Expressed： | Tested and found negative for ectromelia virus (mousepox). immunoglobulin; monoclonal antibody; against mouse macrophage antigen (Mac-2, 32000 dalton glycoprotein),Expression of Mac-2 is increased during the differentiation from monocyte to activated peritoneal macrophage. |
| Cellular Products： | immunoglobulin; monoclonal antibody; against mouse macrophage antigen (Mac-2, 32000 dalton glycoprotein) |
| Comments： | Spleen cells were fused with NS-1 myeloma cells. The Mac-2 antigen is not expressed on bone marrow cells. Like Mac-3, Mac-2 appears to be expressed on the monocytic line of differentiation at a stage after divergence from the granulocytic series. Mac-2 and Mac-3 are present on 69% of macrophages and 0% to 2% of thymocytes. Expression of Mac-2 is increased during the differentiation from monocyte to activated peritoneal macrophage. Tested and found negative for ectromelia virus (mousepox). |
| Complete Growth Medium： | RPMI 1640 medium with 2 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate, 4.5 g/L glucose, 10 mM HEPES, and 1.0 mM sodium pyruvate, 80%; heat-inactivated fetal bovine serum, 20%
RPMI 1640 medium with 2 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate, 4.5 g/L glucose, 10 mM HEPES, and 1.0 mM sodium pyruvate, 80%; heat-inactivated fetal bovine serum, 20% |
| Subculturing： | Protocol: Cultures can be maintained by the addition of fresh medium or replacement of
medium. Adherent cells can be dislodged by scraping and cultures established
by centrifugation with subsequent resuspension at 2 to 4 X 10(5) viable cells/ml.
Interval: Maintain cell density between 2 X 10(5) and 1 X 10(6) viable cells/ml. Medium Renewal: Add fresh medium every 2 to 3 days (depending on cell density) |
| Cryopreservation： | Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO Storage temperature: liquid nitrogen vapor phase |
| Culture Conditions： | Atmosphere: air, 95%; carbon dioxide (CO2), 5% Temperature: 37.0°C |
| Isotype： | rat IgG2a kappa |
| Name of Depositor： | TA Springer |
| Deposited As： | rat (B cell); mouse (myeloma) |
| References： | Ho MK, Springer TA. MAC-2, a novel 32,000 Mr mouse macrophage subpopulation-specific antigen defined by monoclonal antibodies. J. Immunol. 128: 1221-1228, 1982. PubMed: 6173426 Springer TA. Monoclonal antibody analysis of complex biological systems. Combination of cell hybridization and immunoadsorbents in a novel cascade procedure and its application to the macrophage cell surface. J. Biol. Chem. 256: 3833-3839, 1981. PubMed: 7217058 |