PRKX Polyclonal Antibody

    • Catalog No.:YT3859
    • Applications:WB;IHC;IF;ELISA
    • Reactivity:Human;Mouse;Rat
      • Target:
      • PRKX
      • Gene Name:
      • PRKX
      • Protein Name:
      • cAMP-dependent protein kinase catalytic subunit PRKX
      • Human Gene Id:
      • 5613
      • Human Swiss Prot No:
      • P51817
      • Mouse Swiss Prot No:
      • Q922R0
      • Immunogen:
      • The antiserum was produced against synthesized peptide derived from human PRKX. AA range:251-300
      • Specificity:
      • PRKX Polyclonal Antibody detects endogenous levels of PRKX protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:20000.. IF 1:50-200
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • PRKX;PKX1;cAMP-dependent protein kinase catalytic subunit PRKX;PrKX;Protein kinase X;Protein kinase X-linked;Serine/threonine-protein kinase PRKX;Protein kinase PKX1
      • Observed Band(KD):
      • 41kD
      • Background:
      • This gene encodes a serine threonine protein kinase that has similarity to the catalytic subunit of cyclic AMP dependent protein kinases. The encoded protein is developmentally regulated and may be involved in renal epithelial morphogenesis. This protein may also be involved in macrophage and granulocyte maturation. Abnormal recombination between this gene and a related pseudogene on chromosome Y is a frequent cause of sex reversal disorder in XX males and XY females. Pseudogenes of this gene are found on chromosomes X, 15 and Y. [provided by RefSeq, Feb 2010],
      • Function:
      • catalytic activity:ATP + a protein = ADP + a phosphoprotein.,disease:A chromosomal aberration involving PRKX is a cause of sex reversal disorder. Translocation t(X;Y)(p22;p11) with PRKY. Chromosomal translocations proximal to PRKY account for about 30% of the cases of sex reversal disorder in XX males and XY females.,similarity:Belongs to the protein kinase superfamily. AGC Ser/Thr protein kinase family. cAMP subfamily.,similarity:Contains 1 AGC-kinase C-terminal domain.,similarity:Contains 1 protein kinase domain.,tissue specificity:High levels in adult and fetal brain, kidney and lung; low levels in adult placenta, heart, liver, skeletal muscle, pancreas and fetal liver.,
      • Subcellular Location:
      • Cytoplasm. Nucleus. cAMP induces nuclear translocation.
      • Expression:
      • Widely expressed (at protein level). Specifically expressed in blood by macrophages and granulocytes according to PubMed:9860982.
      • Products Images
      • Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PRKX Antibody. The picture on the right is blocked with the synthesized peptide.
      • Western blot analysis of lysates from MCF-7 cells, using PRKX Antibody. The lane on the right is blocked with the synthesized peptide.
      • Western blot analysis of the lysates from HepG2 cells using PRKX antibody.