TIMP3 (C-term) Rabbit Polyclonal Antibody
Other products for "TIMP3"
Specifications
| Product Data | |
| Applications | WB |
| Recommended Dilution | Western blot: At 1-2μg/ml with the appropriate system to detect TIMP-3 in cells and tissues. |
| Reactivities | Human, Mouse, Rat |
| Host | Rabbit |
| Isotype | IgG |
| Clonality | Polyclonal |
| Immunogen | A peptide mapping at the C-terminal end of TIMP-3 of human origin |
| Specificity | This antibody detects TIMP3 (C-term). No cross reactivity with other proteins. |
| Formulation | 5mg BSA, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg Thimerosal, 0.05mg NaN3 State: Aff - Purified State: Lyophilized Ig fraction |
| Reconstitution Method | 0.2ml of distilled water will yield a concentration of 500μg/ml. |
| Purification | Immunogen affinity purified |
| Storage | Store at 2 - 8 °C for up to one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing. |
| Stability | Shelf life: one year from despatch. |
| Gene Name | Homo sapiens TIMP metallopeptidase inhibitor 3 (TIMP3) |
| Database Link | |
| Background | The tissue inhibitors of metalloproteinases (TIMPs) are natural inhibitors of the matrix metalloproteinases, a group of zinc-binding endopeptidases involved in the degradation of the extracellular matrix. The TIMP3 gene is expressed in many tissues, with highest expression in the placenta. TIMP3 encodes a potent angiogenesis inhibitor and is mutated in Sorsby fundus dystrophy, a macular degenerative disease with submacular choroidal neovascularization. TIMP3 gene is mapped to 22q12.1-q13.2. Mutations in TIMP3 cause the autosomal dominant disorder Sorsby's fundus dystrophy (SFD). |
| Synonyms | Protein MIG-5, TIMP-3 |
| Reference Data | |
| Protein Families | Druggable Genome, Secreted Protein |
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