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Validated All-in-One™ qPCR Primer for SETD7(NM_030648.3) Search again
Product ID:
HQP019798
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
KMT7, SET7, SET7/9, SET9
Gene Description:
SET domain containing 7, histone lysine methyltransferase
Target Gene Accession:
NM_030648.3(click here to view gene page)
Estimated Delivery:
Approximately 1-3 weeks, but may vary. Please email sales@genecopoeia.com or call 301-762-0888 to confirm ETA.
Important Note:
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Validated result:
Gene References into function
- purification and functional characterization of a histone H3-lysine 4-specific methyltransferase
- crystal structure of human SET7/9 shows residues essential for catalytic activity with histone H3
- Crystal structure and catalytic mechanism of the human histone methyltransferase SET7/9
- This enzyme and human Sin3 deacetylase are tethered together selectively by the cell-proliferation factor HCF-1.
- SET7/9 recognizes a conserved K/R-S/T/A motif preceding the lysine substrate and has a propensity to bind aspartates and asparagines on the C-terminal side of the lysine target
- RBP2 associates with MRG15 complex to maintain reduced H3K4 methylation at transcribed regions, which may ensure the transcriptional elongation state
- Results suggest that the cross talk between lysine methylation and acetylation is critical for p53 activation in response to DNA damage and that Set7/9 may play an important role in tumor suppression.
- Results show that estrogen receptor alpha is directly methylated at lysine 302 (K302) by the SET7 methyltransferase.
- This report shows that H3K9 monomethylation is dependent upon the PR-Set7 H4K20 monomethyltransferase but independent of its catalytic function, indicating that PR-Set7 recruits an H3K9 monomethyltransferase to establish the trans-tail histone code.
- a novel role for SET7/9 in inflammation and diabetes.
