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  2. Polyclonal

GTX117176

gamma Sarcoglycan antibody

Cannot supply to this region.

SKU:
GTX117176
Additional Names:
sarcoglycan gamma , 35DAG , A4 , DAGA4 , DMDA , DMDA1 , LGMD2C , LGMDR5 , MAM , SCARMD2 , SCG3 , gamma-SG
Application:
WB, IHC-P, IHC-Fr
Concentration:
1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human, Mouse
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Mouse, Rat
Buffer:
PBS, 20% Glycerol, 0.01% Thimerosal.
Immunogen:
Recombinant protein encompassing a sequence within the Extracellular domain of human Gamma Sarcoglycan. The exact sequence is proprietary.
Uniprot:
Q13326
Synonyms:
35 kDa dystrophin-associated glycoprotein;35DAG;35kD dystrophin-associated glycoprotein;A4;DAGA4;DMDA;DMDA1;gamma-sarcoglycan;gamma-SG;LGMD2C;LGMDR5;MAM;sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein);SCARMD2;SCG3
Extra Details:
This 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]
Shipping Conditions:
Blue Ice