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Dysferlin (DYSF) (NM_001130987) Human Recombinant Protein

Product Specifications

Background

The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2008]

Synonyms

FER1L1; LGMD2B; LGMDR2; MMD1

Gene ID

8291

UniProt

O75923

Accession Number mRNA

NM_001130987

Chromosomal Location

2p13.2

Expression System

HEK293T

Tag

C-Myc/DDK

Concentration

>50 ug/mL as determined by microplate BCA method

Purity

> 80% as determined by SDS-PAGE and Coomassie blue staining

Form

Liquid

Buffer

25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

Function

Transmembrane

Molecular Weight

241.2 kDa

Storage Conditions

Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.

Symbol

DYSF

Species

Human

Protein ID

NP_001124459

Overview

Recombinant protein of human dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) (DYSF), transcript variant 1

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/8291

Uniprot URL

https://www.uniprot.org/uniprot/O75923

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_001130987

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_001124459

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