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Rabbit anti-DYSF polyclonal antibody - middle region

Catalog Number:OM112126
OM112126
Discount Price
OM112126-100ul
1~2 Week
100ul
OM112126-50ul
50ul
OM112126-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-DYSF polyclonal antibody - middle region
Antibody Type Primary Antibodies
Antigen Alias FER1L1, FLJ00175, FLJ90168, LGMD2B, MMD1
Immunogen The immunogen for anti-DYSF antibody: synthetic peptide directed towards the middle region of human DYSF
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity BovineDogGuinea PigHorseHumanMousePigRabbitRatZebra Fish
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol DYSF
Gene Synonyms FER1L1
FLJ00175
FLJ90168
LGMD2B
MMD1
Gene Full Name Dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)
Gene Summary DYSF 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, DYSF 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.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alternative Names FER1L1
FLJ00175
FLJ90168
LGMD2B
MMD1
Molecular Weight(MW) 237kDa
Sequence 2080 amino acids
Database Links
Entrez Gene 8291
SwissProt ID O75923
Protein Accession NP_003485
Application

Western blot

0.2-1 ug/mlELISA Titer: 1:12500Positive Control: Human Muscle
Application Notes WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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