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分子生物学
规格：
查看说明书Recombinant Human COMP Protein (His tag)
Cat#:TP07384应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | COMP/Cartilage oligomeric matrix protein Rabbit pAb |
| Cat No.: | DPA01947 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IP |
| Recommended Dilution: | WB: 1:1000 IP: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | Recombinant protein of human COMP/Cartilage oligomeric matrix protein |
| Calculated Molecular Weight: | 83 kDa |
| Observed Molecular Weight: | 110 kDa |
| GenBank Accession Number: | P49747 |
| Gene ID (NCBI): | 1311 |
| Synonyms: | MED; EDM1; EPD1; TSP5; PSACH; THBS5 |
| Background: | The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). [provided by RefSeq, Jul 2016] |
| Category: | Primary Ab |
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