• Western blot analysis of extracts of various cell lines, using SUV39H1 antibody (STJ111182) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (STJS000856) at 1:10000 dilution. Lysates/proteins: 25 Mu g per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s.

Anti-SUV39H1 antibody (1-412) (STJ111182)

SKU:
STJ111182

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Host: Rabbit
Applications: WB/IHC
Reactivity: Human/Mouse/Rat
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit polyclonal antibody anti-SUV39H1 (1-412) is suitable for use in Western Blot and Immunohistochemistry research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: PBS with 0.01% Thimerosal, 50% Glycerol, pH7.3.
Purification: Affinity purification
Dilution Range: WB 1:500-1:1000
IHC-P 1:50-1:200
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: SUV39H1
Gene ID: 6839
Uniprot ID: SUV91_HUMAN
Immunogen Region: 1-412
Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-412 of human SUV39H1 (NP_003164.1).
Immunogen Sequence: MAENLKGCSVCCKSSWNQLQ DLCRLAKLSCPALGISKRNL YDFEVEYLCDYKKIREQEYY LVKWRGYPDSESTWEPRQNL KCVRILKQFHKDLERELLRR HHRSKTPRHLDPSLANYLVQ KAKQRRALRRWEQELNAKRS HLGRITVENEVDLDGPPRAF VYINEYRVGEGITLNQVAVG CECQDCLWAPTGGCCPGASL HKFAYNDQGQVRLRAGLPIY
Post Translational Modifications Phosphorylated on serine residues, and to a lesser degree, on threonine residues. The phosphorylated form is stabilized by SBF1 and is less active in its transcriptional repressor function. Ubiquitinated by the DCX(DCAF13) E3 ubiquitin ligase complex, leading to its degradation. Acetylated at Lys-266, leading to inhibition of enzyme activity. SIRT1-mediated deacetylation relieves this inhibition. (Microbial infection) A higher molecular weight form is also seen in M.bovis infected cells.
Function Histone methyltransferase that specifically trimethylates 'Lys-9' of histone H3 using monomethylated H3 'Lys-9' as substrate. Also weakly methylates histone H1 (in vitro). H3 'Lys-9' trimethylation represents a specific tag for epigenetic transcriptional repression by recruiting HP1 (CBX1, CBX3 and/or CBX5) proteins to methylated histones. Mainly functions in heterochromatin regions, thereby playing a central role in the establishment of constitutive heterochromatin at pericentric and telomere regions. H3 'Lys-9' trimethylation is also required to direct DNA methylation at pericentric repeats. SUV39H1 is targeted to histone H3 via its interaction with RB1 and is involved in many processes, such as repression of MYOD1-stimulated differentiation, regulation of the control switch for exiting the cell cycle and entering differentiation, repression by the PML-RARA fusion protein, BMP-induced repression, repression of switch recombination to IgA and regulation of telomere length. Component of the eNoSC (energy-dependent nucleolar silencing) complex, a complex that mediates silencing of rDNA in response to intracellular energy status and acts by recruiting histone-modifying enzymes. The eNoSC complex is able to sense the energy status of cell: upon glucose starvation, elevation of NAD(+)/NADP(+) ratio activates SIRT1, leading to histone H3 deacetylation followed by dimethylation of H3 at 'Lys-9' (H3K9me2) by SUV39H1 and the formation of silent chromatin in the rDNA locus. Recruited by the large PER complex to the E-box elements of the circadian target genes such as PER2 itself or PER1, contributes to the conversion of local chromatin to a heterochromatin-like repressive state through H3 'Lys-9' trimethylation. (Microbial infection) Plays a role in defense against mycobacterial infections. Methylates M.tuberculosis HupB on 'Lys-140', probably methylates HupB of M.bovis also. Methylation has an inhibitory effect on mycobacterial growth in the host. Macrophages expressing about 60% SUV39H1 are slightly more susceptible to M.bovis or M.tuberculosis infection. Chaetocin (an inhibitor of this enzyme) increases macrophage survival of M.tuberculosis. This protein inhibits biofilm formation by M.tuberculosis via 'Lys-140' trimethylation.
Protein Name Histone-Lysine N-Methyltransferase Suv39h1
Histone H3-K9 Methyltransferase 1
H3-K9-Hmtase 1
Lysine N-Methyltransferase 1a
Position-Effect Variegation 3-9 Homolog
Suppressor Of Variegation 3-9 Homolog 1
Su(Var3-9 Homolog 1
Database Links Reactome: R-HSA-3214841
Reactome: R-HSA-427359
Cellular Localisation Nucleus
Nucleus Lamina
Nucleoplasm
Chromosome
Centromere
Associates With Centromeric Constitutive Heterochromatin
Cytoplasmic Vesicle
Phagosome Lumen
Cell Membrane
(Microbial Infection) Upon Infection With M
Bovis Most Protein Is Found Associated With Bacteria In Phagolysosomes
While Part Is Also Found In The Cell Membrane
Localization Requires Bacterial Hupb
When It Is Deleted Suv39h1 Is Not Phagosomal
Alternative Antibody Names Anti-Histone-Lysine N-Methyltransferase Suv39h1 antibody
Anti-Histone H3-K9 Methyltransferase 1 antibody
Anti-H3-K9-Hmtase 1 antibody
Anti-Lysine N-Methyltransferase 1a antibody
Anti-Position-Effect Variegation 3-9 Homolog antibody
Anti-Suppressor Of Variegation 3-9 Homolog 1 antibody
Anti-Su(Var3-9 Homolog 1 antibody
Anti-SUV39H1 antibody
Anti-KMT1A antibody
Anti-SUV39H antibody

Information sourced from Uniprot.org

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