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SUV39H1 (KMT1A), Active(S350-380G)

SUV39H1 (KMT1A), Active(S350-380G)

  • $259.00


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Description :Recombinant full-length human SUV39H1 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 :Full length

Genbank Number :NM_003173

Specific Activity :Sample Enzyme 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 :Methyltransferase Assay

Molecular Weight :73 kDa

Gene Aliases :KMT1A; MG44; SUV39H

Scientific Background :SUV39H1 is a histone H3-specific methyltransferases that selectively methylates lysine-9 of the N terminus of histone H3 in vitro (1). SUV39H1 is also a member of the suppressor of variegation 3-9 homolog family and encodes a protein with a chromodomain and a C-terminal SET domain. SUV39H1 moves to the centromeres during mitosis where it functions as a histone methyltransferase, methylating Lys-9 of histone H3. SUV39H1 activity is regulated by acetylation at lysine residue 266 in its catalytic SET domain by SIRT1. SIRT1 interacts directly with, recruits, and deacetylates SUV39H1, and these activities independently contribute to elevated levels of SUV39H1 activity resulting in increased levels of the H3K9me3 modification (2).

References :
1. Rea, S.et al: Regulation of chromatin structure by site-specific histone H3 methyltransferases. Nature 406: 593-599, 2000.

2. Vaquero, A. et al: SIRT1 regulates the histone methyl-transferase SUV39H1 during heterochromatin formation. Nature 450: 440-444, 2007.

Product Sheets (By Lot #) :

N330-5.pdf

Q2404-6.pdf

Research Areas :Apoptosis/Autophagy, Cancer, Cell Cycle, Neurobiology