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PHKG1 Antibody (Center)

Catalog Number:OM217061
OM217061
Discount Price
OM217061-100ul
1~2 Week
100ul
OM217061-50ul
50ul
OM217061-20ul
20ul
1~2 Week
Product Profile
Product Name PHKG1 Antibody (Center)
Antibody Type Primary Antibodies
Key Feature
Clonality Polyclonal
Isotype Ig
Host Species Rabbit
Tested Applications WBIHC
WB:1:100~500 IHC
Species Reactivity Human
Concentration 1mg/ml
Target Information
Gene Synonyms PHKG
Alternative Names PHKG1
PHKG
Phosphorylase b kinase gamma catalytic chain
skeletal muscle isoform
Phosphorylase kinase subunit gamma-1
Molecular Weight(MW) 45024 Da
Function Catalytic subunit of the phosphorylase b kinase (PHK), which mediates the neural and hormonal regulation of glycogen breakdown (glycogenolysis) by phosphorylating and thereby activating glycogen phosphorylase. In vitro, phosphorylates PYGM, TNNI3, MAPT/TAU, GAP43 and NRGN/RC3 (By similarity)
Tissue Specificity This PHKG1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 310~339 amino acids from the center region of human PHKG1.
Database Links
Entrez Gene 5260
Application

Application

Western blot analysis of anti-PHKG1 Pab in A375 cell lysate. PHKG1 (arrow) was detected using purified Pab. Secondary HRP-anti-rabbit was used for signal visualization with chemiluminescence.

Application

Formalin-fixed and paraffin-embedded human cancer tissue reacted with the primary antibody, which was peroxidase-conjugated to the secondary antibody, followed by AEC staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated. BC = breast carcinoma; HC = hepatocarcinoma.
Application Notes WB:1:100~500 IHC
Additional Information
Form Liquid
Storage Instructions For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
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