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SGCA antibody
SGCA
Reactivity: Human
WB, IHC, IF
Host: Rabbit
Monoclonal
unconjugated
Product Details anti-SGCA Antibody
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Target
See all SGCA Antibodies
SGCA
(Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
Reactivity
All reactivities for SGCA antibodies
Human
Host
All hosts for SGCA antibodies
Rabbit
Clonality
All clonalities for SGCA antibodies
Monoclonal
Conjugate
All conjugates for SGCA antibodies
This SGCA antibody is un-conjugated
Application
All applications for SGCA antibodies
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
Purpose
alpha Sarcoglycan (SGCA) Rabbit mAb
Cross-Reactivity
Human, Mouse, Rat
Characteristics
Monoclonal Antibodies
Purification
Affinity purification
Immunogen
A synthesized peptide derived from human alpha Sarcoglycan (SGCA) (SGCA)
Isotype
IgG
Top Product
Discover our top product SGCA Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for SGCA
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Target
SGCA
(Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
Alternative Name
SGCA (SGCA Products )
Synonyms
Sgca antibody, 50-DAG antibody, A2 antibody, ADL antibody, DAG2 antibody, DMDA2 antibody, LGMD2D antibody, SCARMD1 antibody, adhalin antibody, 50DAG antibody, Asg antibody, sarcoglycan alpha antibody, sarcoglycan, alpha (dystrophin-associated glycoprotein) antibody, sarcoglycan, alpha antibody, SGCA antibody, Sgca antibody
Background
This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008],50DAG, ADL, DAG2, DMDA2, LGMD2D, SCARMD1, adhalin,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,Signal Transduction,SGCA
Molecular Weight
50kDa
Gene ID
6442
UniProt
Q16586
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