Recombinant Human EMD
| Cat.No. : | EMD-28289TH |
| Product Overview : | Recombinant full length Human Emerin with proprietary tag. Mol Wt 54.01 |
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| Species : | Human |
| Source : | Wheat Germ |
| Tag : | Non |
| Protein Length : | 254 amino acids |
| Description : | Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene. |
| Molecular Weight : | 54.010kDa inclusive of tags |
| Tissue specificity : | Skeletal muscle, heart, colon, testis, ovary and pancreas. |
| Biological activity : | useful for Antibody Production and Protein Array |
| Form : | Liquid |
| Purity : | Proprietary Purification |
| Storage buffer : | pH: 8.00Constituents:0.79% Tris HCl, 0.31% GlutathioneNote: Reduced glutathione |
| Storage : | Shipped on dry ice. Upon delivery aliquot and store at -80oC. Avoid freeze / thaw cycles. |
| Sequence Similarities : | Contains 1 LEM domain. |
| Gene Name | EMD emerin [ Homo sapiens ] |
| Official Symbol | EMD |
| Synonyms | EMD; emerin; Emery Dreifuss muscular dystrophy; LEM domain containing 5; LEMD5; STA; |
| Gene ID | 2010 |
| mRNA Refseq | NM_000117 |
| Protein Refseq | NP_000108 |
| MIM | 300384 |
| Uniprot ID | P50402 |
| Chromosome Location | Xq27.3-q28 |
| Pathway | Arrhythmogenic right ventricular cardiomyopathy (ARVC), organism-specific biosystem; Arrhythmogenic right ventricular cardiomyopathy (ARVC), conserved biosystem; Dilated cardiomyopathy, organism-specific biosystem; Dilated cardiomyopathy, conserved biosystem; Hypertrophic cardiomyopathy (HCM), organism-specific biosystem; |
| Function | actin binding; beta-tubulin binding; protein binding; |
| ◆ Recombinant Proteins | ||
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| ◆ Cell & Tissue Lysates | ||
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Not For Human Consumption!
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