Product Name:

PBK-pY74


Product Number:

ab-pk754

Price:

Regular price
$89.00
Regular price
Sale price
$89.00

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Target Full Name: Lymphokine-activated killer T-cell-originated protein kinase

Target Alias: CT84; FLJ14385; NORI3; SPK; T-LAK cell-originated protein kinase; TOPK; TPOK

Product Type Specific: Protein kinase phosphosite-specific antibody

Antibody Code: PK754

Antibody Target Type: Phosphosite-specific

Antibody Phosphosite: Y74

Protein UniProt: Q96KB5

Protein SigNET: Q96KB5

Antibody Type: Polyclonal

Antibody Host Species: Rabbit

Antibody Immunogen Source: Human PBK sequence peptide Cat. No.: PE-04AOM95

Antibody Immunogen Sequence: NDH(pY)RSV(bA)C

Antibody Immunogen Description: Corresponds to amino acid residues N71 to V77; In the protein kinase catalytic domain between subdomains II and III. This is the major in vivo phosphorylation site in PBK.

Production Method: Corresponds to amino acid residues N71 to V77; In the protein kinase catalytic domain between subdomains II and III. This is the major in vivo phosphorylation site in PBK.

Antibody Modification: Protein kinase phosphosite-specific antibody

Antibody Concentration: 0.5 / 1.0 mg/ml

Storage Buffer: Phosphate buffered saline pH 7.4, 0.05% Thimerasol

Storage Conditions: For long term storage, keep frozen at -40°C or lower. Stock solution can be kept at +4°C for more than 3 months. Avoid repeated freeze-thaw cycles.

Product Use: Western blotting | Antibody microarray

Antibody Dilution Recommended: 2 µg/ml for immunoblotting

Antibody Potency: Very strong immunoreactivity with immunogen peptide on dot blots.

Antibody Species Reactivity: Human

Antibody Positive Control: The observed molecular mass of the processed target protein on SDS-PAGE gels is reported to be around 36-44 kDa.

Antibody Specificity: Very high

Antibody Cross Reactivity: No significant cross-reactive proteins detected in phenylarsine oxide (PAO)+vanadate-treated HeLa cells, EGF-treated A431 cells and insulin-treated MCF7 cells, when these cells were homogenized in SDS-PAGE sample buffer, although strong background >75 kDa was observed.

Related Product 1: PBK-pY74 blocking peptide

Scientific Background: PBK (also known as TOPK) is a protein-serine/threonine kinase that is a member of the Other group of protein kinases in the TOPK family. This kinase shows high variability in human tissue distribution with the highest levels detected in lymph nodes, pituitary, spleen, testes and tonsils. Expression of PKB is particularly detected in male germ line progenitor cells, activated T-cells, and a variety of lymphomas and leukemias. T9 phosphorylation of PBK by CDK1 increases its phosphotransferase activity and induces interaction with CCNB1, CDK1, and tubulin-alpha1. PASK phosphorylates p38 MAPK (but not JNK or ERK1/2) and is activated in a cell-cycle-dependent manner in neuronal progenitor cells in vitro. PBK is active in mitosis and inhibition of the PBK/p38 pathway disrupts neural progentior proliferation and self renewal. In addition, PBK is hypothesized to function in the activation of lymphoid cells. When activated, PBK forms a complex with p53, which destablizes the p53 protein and leads to the attenuation of the G2/M checkpoint for DNA damage. PKB activation requires phosphorylation by both the M-phase CDK1/CyclinB kinase complex and another unknown kinase, possibly Raf1 or RafA. PKB may play an important role in linking extracellular signals to an intracellular state, possibly allowing extracellular influence on the cell-cycle-related processes of proliferation or differentiation. PBK may be an oncoprotein (OP). Gain-of-function mutations in PBK are linked to cancer, specifically plexiform neuroblastoma, as an overactive PBK protein impairs the G2/M checkpoint and prevents cell cycle arrest in the presence of DNA damage. Despite being absent from most normal somatic tissues, PBK has been shown to be significantly upregulated in several cancer types, indicating that gain-of-function mutations may be causing aberrant PBK expression leading to the augmentation of tumour growth in several forms of human cancer.