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Each lot of this antibody is quality control tested by Western blotting. Western blotting, suggested working dilution(s): Use 10 µl per 5 ml antibody dilution buffer for each mini-gel. For IHC, use a 1:50 dilution of antibody for staining. Antigen retrieval using 0.01 M sodium citrate buffer is recommended. It is recommended that the reagent be titrated for optimal performance for each application.
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Hela cells were treated with sodium butyrate for 16 hrs (lane 2) or were untreated (lane 1) and cell extracts prepared. Extracts were western blotted with Poly6171. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.
Formalin-fixed paraffin-embedded human kidney tissue was stained with Poly6171 and developed with an alkaline phosphatase chromogen substate (red color). Tissue was counterstained with H&E (blue/pink). Magnification, 40X.
Dystroglycan (also known as dystrophin-associated glycoprotein 1) is a member of the dystroglycan family that contains the WWW binding motif PPxY. This protein has α and β subunits with approximate molecular weights of 156 kD and 43-50 kD, respectively. The dystroglycan β subunit is an integral membrane protein, the α subunit is a ubiquitously expressed extracellular protein. Muscle and non-muscle isoforms differ by carbohydrate moieties (not protein sequence). Dystroglycan functions as an adhesion molecule responsible for interactions between extracellular matrix and the subsarcolemmal cytoskeleton. Dsytroglycan binds to lamin in the matrix and dystrophin in the cytoskeleton; phosphorylation regulates the association of interacting proteins. Dystroglycan binds to utrophin when unphosphorylated; c-Src, Fyn, Csk, NCK, and SHC when phosphorylated. Dystroglycan interacts with dystrophin through the WW domain. The Poly6171 antibody recognizes human phosphorylated dystroglycan (Tyr893) and has been shown to be useful for Western blotting.
β subunit integral membrane protein, α subunit extracellular; ubiquitously expressed. Muscle and non-muscle isoforms differ by carbohydrate moieties (not protein sequence)
Function:
Adhesion molecule responsible for interactions between extracellular matrix and subsarcolemmal cytoskeleton. Binds to lamin in the matrix and dystrophin in the cytoskeleton
Regulation:
Phosphorylation regulates the association of interacting proteins
Modification:
Phosphorylation
Interaction:
Binds to utrophin when unphosphorylated, c-Src, Fyn, Csk, NCK, and SHC when phosphorylated. Binds to WW domain in dystrophin
Antigen References:
1. Sotgia F, et al. 2001. Biochemistry 40:14585. 2. James M, et al.J. Cell Sci. 113:1717. 3. Huang X, et al. 2000. Nat. Struct. Biol. 7:634.
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Purified anti-Dystroglycan Phospho (Tyr893)
Hela cells were treated with sodium butyrate for 16 hrs (lane 2) or were untreated (lane 1) and cell extracts prepared. Extracts were western blotted with Poly6171. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.
Formalin-fixed paraffin-embedded human kidney tissue was stained with Poly6171 and developed with an alkaline phosphatase chromogen substate (red color). Tissue was counterstained with H&E (blue/pink). Magnification, 40X.