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Validated All-in-One™ qPCR Primer for HDAC9(NM_014707.3) Search again
Product ID:
HQP023134
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
ARCND4, HD7, HD7b, HD9, HDAC, HDAC7, HDAC7B, HDAC9B, HDAC9FL, HDRP, MITR
Gene Description:
histone deacetylase 9
Target Gene Accession:
NM_014707.3(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:
Summary
Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events.
Gene References into function
- Chromosomal organization on chromsome 7
- ICP0 of Herpes simplex virus Type 1 interacts with and controls the repressor activity of class II HDAC7
- The crystal structure of a histone deacetylase 9 (HDAC9)/myocyte enhancer factor-2 (MEF2)/DNA complex reveals that HDAC9 binds to a hydrophobic groove of the MEF2 dimer.
- Moraxella catarrhalis-induced cytokine expression is regulated by acetylation of histone residues and controlled by histone deacetylase activity.
- The role of ACTN4 in MEF2A transcription via HDAC7 antagonism is reported.
- FOXP3 interactions with histone acetyltransferase and class II histone deacetylases are required for repression
- Endogenous HDAC activity plays a crucial role in maintaining the balance of pre-established T(H)1-like and T(H)2-like responses, inhibiting excessive T(H)2 immunity.
- amino enhancer of split has apoptotic activity in neurons and suggest that neuroprotection by histone deacetylase-related protein is mediated by the inhibition of this activity through direct interaction.
