WB result of PNKP Rabbit pAb
Primary antibody: PNKP Rabbit pAb at 1/1000 dilution
Lane 1: HeLa whole cell lysate 20 µg
Lane 2: Jurkat whole cell lysate 20 µg
Lane 3: MDA-MB-231 whole cell lysate 20 µg
Lane 4: Daudi whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 57 kDa
Observed MW: 60 kDa
Product Details
Product Details
Product Specification
Host | Rabbit |
Antigen | PNKP |
Synonyms | Bifunctional polynucleotide phosphatase/kinase, DNA 5'-kinase/3'-phosphatase, Polynucleotide kinase-3'-phosphatase |
Immunogen | Synthetic Peptide |
Location | Nucleus |
Accession | Q96T60 |
Isotype | IgG |
Application | WB |
Reactivity | Hu |
Purification | Protein A |
Concentration | 0.5 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
application | dilution | species |
WB | 1:1000 |
Background
PNKP, which stands for polynucleotide kinase 3'-phosphatase, is an enzyme that plays a significant role in various biological processes, including DNA replication, transcription, and RNA splicing. It is particularly crucial for the repair of DNA strand breaks, participating in both the repair of oxidized DNA bases and the response to DNA damage induced by agents such as ionizing radiation. PNKP possesses both 5′-kinase and 3′-phosphatase activities, which are essential for the phosphorylation of 5′-hydroxyl and removal of 3′-phosphate DNA strand break terminii. The regulation of PNKP is important, as demonstrated by the sensitivity to DNA damaging agents observed in cells with reduced PNKP levels. Furthermore, PNKP's cellular levels are regulated by an E3 ubiquitin ligase complex, which targets the protein for degradation. However, under oxidative stress conditions, phosphorylation of PNKP by protein kinase ATM inhibits this ubiquitylation-dependent degradation, leading to increased PNKP protein levels required for DNA repair. Mutations in the PNKP have been associated with autosomal recessive disorders characterized by severe neurological abnormalities, such as microcephaly, early-onset seizures, and developmental delay.
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Picture
Western Blot
