"EMD" Related Products

Recombinant Human EMD

Cat.No.: EMD-28289TH
Product Overview: Recombinant full length Human Emerin with proprietary tag. Mol Wt 54.01
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.
Protein length: 254 amino acids
Molecular Weight: 54.010kDa inclusive of tags
Source: Wheat germ
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;

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