SGCG rabbit pAb

SGCG rabbit pAb

AO-06-ES13136-100

SGCG rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES13136
Product nameSGCG rabbit pAb
ReactivityHuman; Mouse
ApplicationsWB;IHC
Other name
Size100μL
Unit price ($)248
Human gene ID6445
Human Swiss-ProtQ13326
SourceRabbit
IsotypeIgG
TargetSGCG
Fields>>Hypertrophic cardiomyopathy;>>Arrhythmogenic right ventricular cardiomyopathy;>>Dilated cardiomyopathy;>>Viral myocarditis
Gene nameSGCG
Protein nameSGCG
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID24053
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP82348
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human SGCG AA range: 213-263
SpecificityThis antibody detects endogenous levels of SGCG at Human/Mouse
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)32kD
Observed band (KD)
BackgroundThis gene encodes gamma-sarcoglycan, one of several sarcolemmal transmembrane glycoproteins that interact with dystrophin. The dystrophin-glycoprotein complex (DGC) spans the sarcolemma and is comprised of dystrophin, syntrophin, alpha- and beta-dystroglycans and sarcoglycans. The DGC provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix of muscle cells. Defects in the encoded protein can lead to early onset autosomal recessive muscular dystrophy, in particular limb-girdle muscular dystrophy, type 2C (LGMD2C). [provided by RefSeq, Oct 2008],
Functiondisease:Defects in SGCG are the cause of limb-girdle muscular dystrophy type 2C (LGMD2C) [MIM:253700]. LGMD2C is characterized by progressive muscle wasting from early childhood.,function:Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix.,online information:SGCG mutations in LGMD2C,similarity:Belongs to the sarcoglycan beta/delta/gamma/zeta family.,subunit:Interacts with the syntrophin SNTA1. Cross-link to form 2 major subcomplexes: one consisting of SGCB, SGCD and SGCG and the other consisting of SGCB and SGCD. The association between SGCB and SGCG is particularly strong while SGCA is loosely associated with the other sarcoglycans (By similarity). Interacts with FLNC.,tissue specificity:Expressed in skeletal and heart muscle.,
Subcellular locationCell membrane, sarcolemma ; Single-pass type II membrane protein . Cytoplasm, cytoskeleton .
ExpressionExpressed in skeletal and heart muscle.

Additional Images

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Western blot analysis of lysates from K562 cells, primary antibody was diluted at 1:1000, 4°over night
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Immunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
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: AO-06-ES13136-100
: 10 Produits
Hurry! only 10 items left in stock.

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