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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| RFL19648HF | Recombinant Full Length Human Emerin(Emd) Protein, His-Tagged | +Inquiry | 
| ◆ Cell & Tissue Lysates | ||
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Not For Human Consumption!
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