| 产品名称： | 548 |
|---|---|
| 商品货号： | TS212833 |
| Organism： | Mus musculus (B cell); Mus musculus (myeloma), mouse (B cell); mouse (myeloma) |
| 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. |
| Disease： | Leukemia |
| Applications： | The antibody reacts with the p12 protein of most MuLV. The antibody reacts with infected cells after acetone or methanol fixation and immunoprecipitates p12. |
| Storage Conditions： | liquid nitrogen vapor phase |
| Derivation： | Spleen cells from a mouse recovering from splenomegaly induced by Moloney murine leukemia virus (MoMuLV) and Spleen Focus Forming virus (SFFV) were fused with NS-1 myeloma cells. |
| Genes Expressed： | immunoglobulin; monoclonal antibody; against p12 group antigen (GAG) protein of murine leukemia viruses (MuLV) |
| Cellular Products： | immunoglobulin; monoclonal antibody; against p12 group antigen (GAG) protein of murine leukemia viruses (MuLV) |
| Comments： | Spleen cells from a mouse recovering from splenomegaly induced by Moloney murine leukemia virus (MoMuLV) and Spleen Focus Forming virus (SFFV) were fused with NS-1 myeloma cells. The antibody reacts with the p12 protein of most MuLV. The antibody reacts with infected cells after acetone or methanol fixation and immunoprecipitates p12. |
| Complete Growth Medium： | RPMI 1640 medium with 0.05 mM 2-mercaptoethanol, 90%; fetal bovine serum, 10%
|
| Subculturing： | Cultures can be maintained by addition or replacement of fresh medium. Start cultures at 2 x 105 cells/mL and maintain between 1 x 105 and 1 x 106 cells/mL. Medium Renewal: Every 2 to 3 days |
| Cryopreservation： | Complete growth medium described above supplemented with 5% (v/v) DMSO.xa0 Cell culture tested DMSO is available as ATCC Catalog No. 4-X. |
| Culture Conditions： | Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5% |
| Isotype： | IgG2b |
| Name of Depositor： | B Chesebro |
| Deposited As： | mouse (B cell); mouse (myeloma) |
| References： | Chesebro B, et al. Characterization of monoclonal antibodies reactive with murine leukemia viruses: Use in analysis of strains of Friend MCF and Friend ecotropic murine leukemia virus. Virology 127: 134-148, 1983. PubMed: 6305011 Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC. Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988. Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC. Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online. |
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| 产品名称： | 548 |
|---|---|
| 商品货号： | TS212833 |
| Organism： | Mus musculus (B cell); Mus musculus (myeloma), mouse (B cell); mouse (myeloma) |
| 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. |
| Disease： | Leukemia |
| Applications： | The antibody reacts with the p12 protein of most MuLV. The antibody reacts with infected cells after acetone or methanol fixation and immunoprecipitates p12. |
| Storage Conditions： | liquid nitrogen vapor phase |
| Derivation： | Spleen cells from a mouse recovering from splenomegaly induced by Moloney murine leukemia virus (MoMuLV) and Spleen Focus Forming virus (SFFV) were fused with NS-1 myeloma cells. |
| Genes Expressed： | immunoglobulin; monoclonal antibody; against p12 group antigen (GAG) protein of murine leukemia viruses (MuLV) |
| Cellular Products： | immunoglobulin; monoclonal antibody; against p12 group antigen (GAG) protein of murine leukemia viruses (MuLV) |
| Comments： | Spleen cells from a mouse recovering from splenomegaly induced by Moloney murine leukemia virus (MoMuLV) and Spleen Focus Forming virus (SFFV) were fused with NS-1 myeloma cells. The antibody reacts with the p12 protein of most MuLV. The antibody reacts with infected cells after acetone or methanol fixation and immunoprecipitates p12. |
| Complete Growth Medium： | RPMI 1640 medium with 0.05 mM 2-mercaptoethanol, 90%; fetal bovine serum, 10%
|
| Subculturing： | Cultures can be maintained by addition or replacement of fresh medium. Start cultures at 2 x 105 cells/mL and maintain between 1 x 105 and 1 x 106 cells/mL. Medium Renewal: Every 2 to 3 days |
| Cryopreservation： | Complete growth medium described above supplemented with 5% (v/v) DMSO.xa0 Cell culture tested DMSO is available as ATCC Catalog No. 4-X. |
| Culture Conditions： | Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5% |
| Isotype： | IgG2b |
| Name of Depositor： | B Chesebro |
| Deposited As： | mouse (B cell); mouse (myeloma) |
| References： | Chesebro B, et al. Characterization of monoclonal antibodies reactive with murine leukemia viruses: Use in analysis of strains of Friend MCF and Friend ecotropic murine leukemia virus. Virology 127: 134-148, 1983. PubMed: 6305011 Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC. Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988. Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC. Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online. |
