| 產(chǎn)品名稱(chēng) |
LM2/1.6.11 |
| 商品貨號(hào) |
B164991 |
| Organism |
Mus musculus (B cell); Mus musculus (myeloma), mouse (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 |
The antibody reacts with the human Mac-1 antigen and is specific for the alpha chain. The depositor states that the cell line should not be maintained in culture continuously for greater than four months or antibody production may be lost. Cloning and freezing of the cells after minimal passage (with selection of positive clones) will prevent loss of antibody producing cells. Tested and found negative for ectromelia virus (mousepox). |
| Storage Conditions |
liquid nitrogen vapor phase |
| Derivation |
Spleen cells were fused with P3X63Ag8.653 myeloma cells. |
| Genes Expressed |
immunoglobulin; monoclonal antibody; against human Mac-1 antigen; against CD11b |
| Cellular Products |
immunoglobulin; monoclonal antibody; against human Mac-1 antigen; against CD11b |
| Comments |
Animals were immunized with immunoprecipitates of human granulocyte lysates using TS1/18 (see ATCC HB-203) and boosted with live human granulocytes. Spleen cells were fused with P3X63Ag8.653 myeloma cells. The antibody reacts with the human Mac-1 antigen and is specific for the alpha chain. The depositor states that the cell line should not be maintained in culture continuously for greater than four months or antibody production may be lost. Cloning and freezing of the cells after minimal passage (with selection of positive clones) will prevent loss of antibody producing cells. Tested and found negative for ectromelia virus (mousepox). |
| Complete Growth Medium |
The base medium for this cell line is ATCC Hybri-Care Medium, Catalog No. 46-X. Hybri-Care Medium is supplied as a powder and should be reconstituted in 1 L cell-culture-grade water and supplemented with 1.5 g/L sodium bicarbonate. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
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| Subculturing |
Protocol: 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 1 X 10(5) viable cells/ml. Subcultivation Ratio: Maintain cell density between 1 X 10(5) and 1 X 10(6) viable cells/ml. Medium Renewal: Every 2 to 3 days |
| Cryopreservation |
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO Storage temperature: liquid nitrogen vapor phase |
| Culture Conditions |
Temperature: 37.0°C |
| Isotype |
mouse IgG1 |
| Name of Depositor |
LJ Miller, TA Springer |
| Deposited As |
mouse (B cell); mouse (myeloma) |
| Passage History |
Cloning and freezing of the cells after minimal passage (with selection of positive clones) will prevent loss of antibody producing cells. |
| References |
Miller LJ, et al. Regulated expression of the Mac-1, LFA-1, p150,95 glycoprotein family during leukocyte differentiation. J. Immunol. 137: 2891-2900, 1986. PubMed: 2428876
Zhang L, Plow EF. Overlapping, but not identical, sites are involved in the recognition of C3bi, neutrophil inhibitory factor, and adhesvie ligands by the alpha M beta 2 integrin. J. Biol. Chem. 271: 18211-18216, 1996. PubMed: 8663418
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