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HIPK1, Active(H03-11G)

HIPK1, Active(H03-11G)

  • $226.00


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Description :Recombinant human HIPK1 (156-555) was expressed by baculovirus in Sf9 insect cells using an N-terminal GST tag.

Species :Human

Tag :GST tag

Expression System:Sf9 insect cells using baculovirus

Sequence :156-555

Genbank Number :NM_152696

Specific Activity :Sample Kinase Activity Plot. For specific information on a given lot, see related technical data sheet.

Purity :Sample Purity Data. For specific information on a given lot, see related technical data sheet.

Storage, Stability and Shipping :Store product at –70oC. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.

Applications :Kinase Assay, Western Blot

Molecular Weight :~71 kDa

Gene Aliases :Myak, Nbak2, KIAA0630, MGC26642, MGC33446, MGC33548

Scientific Background :HIPK1 or homeodomain-interacting protein kinase 1 is a ser/thr protein kinase and a member of the HIPK family. HIPK 1 is a nuclear kinase that phosphorylates homeodomain transcription factors. HIPK1 phosphorylates DAXX and this leads to its relocalization and subsequent decrease in transcriptional repression activity (1). HIPK1also interacts with p53 and phosphorylates it on serine residues. HIPK 1 expression is elevated in breast cancer cell lines and embryonic fibroblasts from HIPK 1-null mice show more susceptibility to apoptosis induced by DNA damage (2).

References :
1. Ecsedy, J A. et al: Homeodomain-interacting protein kinase 1 modulates Daxx localization, phosphorylation, and transcriptional activity. Mol Cell Biol. 2003 Feb;23(3):950-60.

2. Kondo, S. et al: Characterization of cells and gene-targeted mice deficient for the p53-binding kinase homeodomain-interacting protein kinase 1 (HIPK1). Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5431-6.

Product Sheets (By Lot #) :

P263-1.pdf

U1693-7.pdf

Research Areas :Cancer, Metabolic Disorder, WNT Signaling, Cell Cycle, Ser/Thr Kinases, Cancer, Metabolic Disorder, WNT Signaling, Cell Cycle, Ser/Thr Kinases