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Defects in SGCD are the cause of limb-girdle muscular dystrophy type 2F (LGMD2F) [MIM:601287]
DF10261-200
Catalogue Numbers: BS8317-50
Specificity: Phospho-SIRT1 (S47) Antibody detects endogenous levels of Phospho-SIRT1 (S47)
Phospho-AKT1-S473 Polyclonal Antibody-BS79347 Size:100µl Defects in SGCD are thePhospho AKT1 S473 Polyclonal Antibody Sizes: 50l, 100l Catalogue Numbers: BS79347 50, BS79347 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: P31749 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, IHC, IP, All Applications: WB,1: 500 1: 2000 IHC,1: 50 1: 200 IP,1: 50 1: 100 Background: The serine threonine protein kinase encoded by the AKT1 gene is catalytically inactive in serum starved primary and
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