SKU: WM0153 Categories: ,

EHMT1 Monoclonal Antibody

Price range: $268.00 through $328.00

SKU: WM0153-50
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Product details

Background:
The protein encoded by this gene is a histone methyltransferase that is part of the E2F6 complex, which represses transcription. The encoded protein methylates the Lys-9 position of histone H3, which tags it for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014],

Specifications

Size50μL/100μL
TargetEHMT1
ReactivityHuman
ApplicationsWB, ELISA
MW(Calculated)141kD
MW(Observed)
Host SpeciesMouse
Isotype
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; ELISA 1:10000; Not yet tested in other applications.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationAffinity purification
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone Number6D12
ImmunogenPurified recombinant fragment of EHMT1 expressed in E. Coli.
SpecificityEHMT1 Monoclonal Antibody detects endogenous levels of EHMT1 protein.
Gene NameEHMT1
Protein NameHistone-lysine N-methyltransferase, H3 lysine-9 specific 5
Other NameEHMT1; / EUHMTASE1; / GLP; / KIAA1876; / KMT1D; / Histone-lysine N-methyltransferase EHMT1; / Euchromatic histone-lysine N-methyltransferase 1; / Eu-HMTase1; / G9a-like protein 1; / GLP; / GLP1; / Histone H3-K9 methyltransferase 5; / H3-K9-HMTase 5; / Lysine N-methy
SpeciesHuman
Gene ID79813
UniprotQ9H9B1,
Species.1Mouse
Gene ID.1
Uniprot.1Q5DW34
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationNucleus. Chromosome. Associates with euchromatic regions.
Tissue ExpressionWidely expressed.
Signaling_pathwayOrganismal Systems >> Aging >> Longevity regulating pathway
Research Areas>>Lysine degradation; / >>Metabolic pathways; / >>Longevity regulating pathway
FunctionAlternative products:Experimental confirmation may be lacking for some isoforms,Catalytic activity:S-adenosyl-L-methionine + histone L-lysine = S-adenosyl-L-homocysteine + histone N(6)-methyl-L-lysine.,Disease:Defects in EHMT1 are the cause of chromosome 9q subtelomeric deletion syndrome (9q- syndrome) [MIM:610253]. Common features seen in these patients are severe mental retardation, hypotonia, brachy(micro)cephaly, epileptic seizures, flat face with hypertelorism, synophrys, anteverted nares, cupid bow or tented upper lip, everted lower lip, prognathism, macroglossia, conotruncal heart defects, and behavioral problems.,Domain:The SET domain mediates interaction with WIZ.,Function:Histone methyltransferase. Methylates 'Lys-9' of histone H3 (in vitro). H3 'Lys-9' methylation represents a specific tag for epigenetic transcriptional repression by recruiting HP1 proteins to methylated histones. Probably targeted to histone H3 by different DNA-binding proteins like E2F6, MGA, MAX and/or DP1. During G0 phase, it probably contributes to silencing of MYC- and E2F-responsive genes, suggesting a role in G0/G1 transition in cell cycle.,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,sequence Caution:Intron retention.,similarity:Belongs to the histone-lysine methyltransferase family.,similarity:Contains 1 pre-SET domain.,similarity:Contains 1 SET domain.,similarity:Contains 8 ANK repeats.,subcellular location:Associates with euchromatic regions.,subunit:Part of the E2F6.com-1 complex in G0 phase composed of E2F6, MGA, MAX, TFDP1, CBX3, BAT8, EUHMTASE1, RING1, RNF2, MBLR, L3MBTL2 and YAF2. Interacts with WIZ and EHMT2.,tissue specificity:Widely expressed.,
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