PHKA1/2 rabbit pAb

PHKA1/2 rabbit pAb

AO-06-ES6584-50

PHKA1/2 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES6584
Product namePHKA1/2 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA;IHC
Other namePHKA1; PHKA; Phosphorylase b kinase regulatory subunit alpha; skeletal muscle isoform; Phosphorylase kinase alpha M subunit; PHKA2; PHKLA; PYK; Phosphorylase b kinase regulatory subunit alpha, liver isoform; Phosphorylase kinase alpha L sub
Size50μL
Unit price ($)148
Human gene ID5255/5256
Human Swiss-ProtP46020/P46019
SourceRabbit
IsotypeIgG
TargetPHKA1/2
Fields>>Calcium signaling pathway;>>Insulin signaling pathway;>>Glucagon signaling pathway
Gene namePHKA1/PHKA2
Protein namePhosphorylase b kinase regulatory subunit alpha skeletal muscle isoform/Phosphorylase b kinase regulatory subunit alpha liver isoform
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID18679/110094
Mouse gene linkView Mouse Gene
Mouse Swiss-Prot
Mouse Swiss link
Rat gene ID64561
Rat gene linkView Rat Gene
Rat Swiss-ProtQ64649
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human KPB1/2. AA range:31-80
SpecificityPHKA1/2 Polyclonal Antibody detects endogenous levels of PHKA1/2 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)137kD
BackgroundPhosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, and the skeletal muscle isoform is encoded by this gene. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, which are encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9D, also known as X-linked muscle glycogenosis. Alternatively spliced transcript varian
Functiondisease:Defects in PHKA1 are the cause of glycogen storage disease type 9D (GSD9D) [MIM:300559]; also known as X-linked muscle glycogenosis. GSD9D is a metabolic disorder characterized by slowly progressive, predominantly distal muscle weakness and atrophy. Clinical features include exercise intolerance with early fatiguability, pain, cramps and occasionally myoglobinuria.,enzyme regulation:By phosphorylation of various serine residues. Allosteric regulation by calcium.,function:Phosphorylase b kinase catalyzes the phosphorylation of serine in certain substrates, including troponin I. The alpha chain may bind calmodulin.,pathway:Glycan biosynthesis; glycogen metabolism.,similarity:Belongs to the phosphorylase b kinase regulatory chain family.,subunit:Polymer of 16 chains, four each of alpha, beta, gamma, and delta. Alpha and beta are regulatory chains, gamma is the catalytic chain, and d
Subcellular locationCell membrane ; Lipid-anchor ; Cytoplasmic side .
ExpressionMuscle specific. Isoform 1 is predominant in vastus lateralis muscle. Isoform 2 predominates slightly in heart, and it predominates clearly in the other tissues tested.

Additional Images

Image 1
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Immunofluorescence analysis of HeLa cells, using KPB1/2 Antibody. The picture on the right is blocked with the synthesized peptide.
Image 2
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Western blot analysis of lysates from Jurkat and COLO205 cells, using KPB1/2 Antibody. The lane on the right is blocked with the synthesized peptide.
Image 3
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Immunohistochemical analysis of paraffin-embedded human uterus. 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-ES6584-50
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