hsMAD2 (AA 27-172) antibody
| Antigen | hsMAD2 |
| Binding Site |
AA 27-172 |
| Clonality | Monoclonal (48) |
| Host |
Mouse |
| Reactivity |
Human |
| Application |
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
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5 references available |
| Catalog no. | ABIN968105 |
| Quantity |
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| Price | Product not available in this region. |
| Shipping to |
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Additional Information
| Immunogen | Human MAD2 |
| Cross-Reactivity | Mouse (Murine), Rat (Rattus) |
| Format | Liquid |
| Isotype | IgG2a |
| Clone | 48 |
| Description |
Progression of the mammalian cell cycle is regulated by phosphorylation/dephosphorylation and synthesis/degradation of many key proteins. These events are of utmost importance at the checkpoints, or transition points, of the cell cycle. MAD2 (Mitotic Arrest Deficient) is the human homolog of a yeast and Xenopus protein that is essential for spindle assembly during mitosis. The human hsMAD2 gene encodes a protein of 205 amino acids with a predicted molecular weight of 23.5 kDa. Binding of affinity purified polyclonal antibodies to the MAD2 protein prevents mitosis of HeLa cells. This indicates that, like its invertebrate relatives, MAD2 is necessary for mitosis. Furthermore, MAD2 is localized at the kinetochore of condensed chromosomes during mitosis and cells defective in the mitotic checkpoint have reduced levels of MAD2. Synonyms: Mitotic Arrest Deficient-2 |
| Characteristics |
1. Since applications vary, each investigator should titrate the reagent to obtain optimal results. 2. Please refer to us for technical protocols. 3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing. 4. Source of all serum proteins is from USDA inspected abattoirs located in the United States. |
| Molecular Weight | 24 kDa |
| Comments |
Related Products: ABIN968537, ABIN967389 |
Application Details
| Concentration | 250 µg/ml |
| Purity | Purified |
| Purification | Purified from tissue culture supernatant or ascites by affinity chromatography. |
| Buffer | Aqueous buffered solution containing BSA, glycerol. |
| Preservative | 0.09% Sodium azide. |
| Storage | Store undiluted at -20° C. |
| Restrictions | For Research Use only |
Images
Publications
| Product |
Chen, Waters, Salmon et al.: "Association of spindle assembly checkpoint component XMAD2 with unattached kinetochores." in: Science (New York, N.Y.), Vol. 274, Issue 5285, pp. 242-6, 1996 (PubMed).
Li, Benezra: "Identification of a human mitotic checkpoint gene: hsMAD2." in: Science (New York, N.Y.), Vol. 274, Issue 5285, pp. 246-8, 1996 (PubMed). Saitoh, Pizzi, Wang: "Perturbation of SUMOlation enzyme Ubc9 by distinct domain within nucleoporin RanBP2/Nup358." in: The Journal of biological chemistry, Vol. 277, Issue 7, pp. 4755-63, 2002 (PubMed). Iwanaga, Kasai, Kibler et al.: "Characterization of regions in hsMAD1 needed for binding hsMAD2. A polymorphic change in an hsMAD1 leucine zipper affects MAD1-MAD2 interaction and spindle checkpoint function." in: The Journal of biological chemistry, Vol. 277, Issue 34, pp. 31005-13, 2002 (PubMed). Babu, Jeganathan, Baker et al.: "Rae1 is an essential mitotic checkpoint regulator that cooperates with Bub3 to prevent chromosome missegregation." in: The Journal of cell biology, Vol. 160, Issue 3, pp. 341-53, 2003 (PubMed). |




