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
Curated Selection
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