recommended for detection of Ser 246 phosphorylated HDAC4 of human origin and correspondingly phosphorylated Ser 245 of mouse origin; Ser 259 phosphorylated HDAC5 of human origin and correspondingly phosphorylated Ser 250 of mouse origin and Ser 200 phosph
Modification
Phosphoralated
Modification Notes
In the intact cell, DNA closely associates with histones and other nuclear proteins to form chromatin. The remodeling of chromatin is believed to be a critical component of transcriptional regulation and a major source of this remodeling is brought about by the acetylation of nucleosomal histones. Acetylation of lysine residues in the amino terminal tail domain of histone results in an allosteric change in the nucleosomal conformation and an increased accessibility to transcription factors by DNA. Conversely, the deacetylation of histones is associated with transcriptional silencing. The histone deacetylases (HDAC) include HDAC1–9. Subject to post-translational modifications, HDAC4, 5 and 9 contain phosphoserine residues at Ser-246, Ser-259 and Ser-220, respectively.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIP
WB:1:500~1:2000 IP:1:100~1:500 Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of Ser 246 phosphorylated HDAC4 of human origin and correspondingly phosphorylated Ser 245 of mouse origin Ser 259 phosphorylated HDAC5 of human origin and correspondingly phosphorylated Ser 250 of mouse origin and Ser 200 phosph
Tissue Specificity
recommended for detection of Ser 246 phosphorylated HDAC4 of human origin and correspondingly phosphorylated Ser 245 of mouse origin; Ser 259 phosphorylated HDAC5 of human origin and correspondingly phosphorylated Ser 250 of mouse origin and Ser 200 phosphorylated HDAC9 of human and mouse origin by WB and IP