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Validated All-in-One™ qPCR Primer for HDAC5(NM_001015053.1) Search again
Product ID:
HQP000023
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
HD5, NY-CO-9
Gene Description:
histone deacetylase 5
Target Gene Accession:
NM_001015053.1(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:
Summary
Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events.
Gene References into function
- Class II histone deacetylases are directly recruited by BCL6 transcriptional repressor
- Histone deacetylase 5 is not a p53 target gene, but its overexpression inhibits tumor cell growth and induces apoptosis.
- MITR, HDAC4, and HDAC5 associate with heterochromatin protein 1 (HP1), an adaptor protein that recognizes methylated lysines within histone tails and mediates transcriptional repression by recruiting histone methyltransferase
- HDAC5 binds to Ca(2+)/calmodulin and inhibits MEF2a binding
- ICP0 of herpes simplex virus Type 1 is able to overcome the HDAC5 amino-terminal- and MITR-induced MEF2A repression in gene reporter assays
- The HDAC5, a class II HDAC involved in myogenesis, was not detected in the tissues.
- G betagamma binds HDAC5 and inhibits its transcriptional co-repression activity
- novel transcriptional pathway under the control of class II HDACs and suggest a role for these transcriptional repressors as signal-responsive regulators of antigen presentation
- NO-dependent PP2A activation plays a key role in nuclear translocation of class II HDACs HDAC4 and HDAC5
- AMP-activated protein kinase (AMPK) regulates GLUT4 transcription through the histone deacetylase (HDAC)5 transcriptional repressor.
- Chronic upregulation/activation of CaMKIID, and PKD in heart failure shifts HDAC5 out of the nucleus, derepressing transcription of hypertrophic genes.
- Protein kinase D-HDAC5 pathway plays an important role in VEGF regulation of gene transcription and angiogenesis
- These results indicate that HDAC4 and HDAC5 increase the transactivation function of HIF-1alpha by promoting dissociation of HIF-1alpha from FIH-1 and association with p300.
