- Antibody Type
- Polyclonal
- Target
- Phospho-HDAC4 (Ser632)/HDAC5 (Ser661)/HDAC7 (Ser486)
- Reactivity
- Human, Mouse
- Application
- WB
- MW(Calculated)
- 140 kDa / 140 kDa / 100 kDa
- MW(Observed)
- --
- Host Species
- Rabbit
- Isotype
- IgG
- Conjugate
- Unconjugated
- Modification
- Phosphorylation
- Modification Site
- HDAC4 Ser632, HDAC5 Ser661, HDAC7 Ser486
- Recommended dilution ratio
- WB 1:1000-1:2000
- Composition
- PBS, Glycerol, BSA
- Purification process
- Protein A affinity purification
- storageCondition
- Store at -20°C. Avoid repeated freeze-thaw cycles
- Stability
- Stable for 12 months from date of receipt / reconstitution.
- Concentration
- --
- Clonal
- Polyclonal
- Clone Number
- --
- Immunogen
- polypeptide
- Gene Name
- HDAC4, HDAC5, HDAC7
- Protein Name
- Histone deacetylase 4 / Histone deacetylase 5 / Histone deacetylase 7
- Alternative name
- --
- Organism-1
- Human
- Gene ID
- HDAC4: 9759; HDAC5: 10014; HDAC7: 51534
- SwissProt-1
- HDAC4: P56524; HDAC5: Q9UQL6; HDAC7: Q8WUI4
- --
- Background:
- Background
- Histone deacetylase 4, also known as HDAC4, is a protein that is encoded by the HDAC4 gene in human. Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. This protein does not bind DNA directly but through transcription factors MEF2C and MEF2D. Furthermore, HDAC4 is required for TGFbeta1-induced myofibroblastic differentiation. In addition, the highly conserved HDAC4 Ser632, HDAC5 Ser498 (Ser661) and HDAC7 Ser486 residues are all phosphorylated by CAMK and PKD kinases in response to multiple cell stimuli, including VEGF-induced angiogenesis in endothelial cells, B cell and T cell activation, and differentiation of myoblasts into muscle fiber.
- Cellular Localization
- Nucleus. Cytoplasm
- --
- Background:Histone deacetylase 4, also known as HDAC4, is a protein that is encoded by the HDAC4 gene in human. Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. This protein does not bind DNA directly but through transcription factors MEF2C and MEF2D. Furthermore, HDAC4 is required for TGFbeta1-induced myofibroblastic differentiation. In addition, the highly conserved HDAC4 Ser632, HDAC5 Ser498 (Ser661) and HDAC7 Ser486 residues are all phosphorylated by CAMK and PKD kinases in response to multiple cell stimuli, including VEGF-induced angiogenesis in endothelial cells, B cell and T cell activation, and differentiation of myoblasts into muscle fiber.
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