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| Catalog Code: | NB100-78188 |
| Product Name: | GM-CSF Antibody |
| Product Description: | Rat Monoclonal anti-GM-CSF (MP1-22E9), conjugated to FITC |
| Clone: | MP1-22E9 |
| Clonality: | Monoclonal |
| ListPrice: | 295 |
| Immunogen: | Yeast-expressed, recombinant mouse GM-CSF. |
| Cross Reactivity: | Mouse. |
| Packaging: | 0.1 mg Immunogen affinity purified Rat antisera |
| Uses: | Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For immunofluorescent staining, the suggested use of this reagent is: 0.25 microgram per one million cells in 100 microliter volume. It is recommended that the reagent be titrated for optimal performance for each application. |
| Background: | GM-CSF is a hematopoietic factor that is produced by T cells, macrophages, fibroblasts and endothelial cells. This multifunctional cytokine stimulates progenitor cells of neutrophils, eosinophils and macrophages. GM-CSF is also a differentiation and activating factor for granulocytic and monocytic cells. The MP1-22E9 antibody reacts with mouse granulocyte/macrophage-colony stimulating factor (GM-CSF). The MP1-22E9 antibody can neutralize the bioactivity of natural or recombinant GM-CSF. |
| Storage: | Store at 4C. Do not freeze. |
| Purity: | Immunogen affinity purified |
| Isotype: | IgG2a, kappa |
| Host Name: | Rat |
| Buffer: | Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide. |
| Application Summary: | Immunocytochemistry, flow cytometry / FACS analysis |
| Species Summary: | Mu |
| Alternate Names: | anti-Granulocyte/macrophage-colony stimulating factor antibody, anti-CSF-alpha; antibody, anti-Pluripoietin-α antibody, anti-Eosinophil colony stimulating factor (Eo-CSF) antibody, anti-Burst promoting activity (BPA) antibody, anti-GM CSF antibody |
| Package Size: | 0.1 mg |
| Conjugate: | FITC |
| General References: | 1. Fitzgerald, K., et al., Eds. 2001. The Cytokine FactsBook. Academic Press, San Diego. 2. Demetri, G., et al., 1991. Blood 78:2791. 3. Fan, D., et al., 1991. In vivo 5:571. |
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