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Human Dystrophin (DMD) ELISA Kit

Cat no: KTE62014


Supplier: Abbkine Scientific Co.Ltd.
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Dystrophin is a rod-shaped cytoplasmic protein, and a vital part of a protein complex that connects the cytoskeleton of a muscle fiber to the surrounding extracellular matrix through the cell membrane. This complex is variously known as the costamere or the dystrophin-associated protein complex. Many muscle proteins, such as ?-dystrobrevin, syncoilin, synemin, sarcoglycan, dystroglycan, and sarcospan, colocalize with dystrophin at the costamere. The DMD gene, encoding the dystrophin protein, is one of the longest human genes known, covering 2.3 megabases (0.08% of the human genome) at locus Xp21. The primary transcript in muscle measures about 2,100 kilobases and takes 16 hours to transcribe; the mature mRNA measures 14.0 kilobases. The 79-exon muscle transcript[5] codes for a protein of 3685 amino acid residues.
Catalogue number: KTE62014
Reactivities: Human
Applications: ELISA
Size: 48T, 96T, 96T*5, 96T*50
Accession: P11532
Gene: 1756
Additional info: Human Dystrophin (DMD) ELISA Kit has high sensitivity and excellent specificity for detection of Human DMD. No significant cross-reactivity or interference between Human DMD and analogues was observed.

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