epitope corresponding to amino acids 400-706 mapping at the carboxy terminus of HDA1 of Saccharomyces cerevisiae origin
Modification Notes
Remodeling of chromatin structure is believed to be a critical component of transcriptional regulation. A major source of remodeling is brought about by the acetylation of nucleosomal histones. Acetylation results in an allosteric change in the nucleosomal conformation and an increased accessibility of DNA to transcription factors. Conversely, the deacetylation of histones is associated with transcriptional silencing. HDA1, HDA2, HDA3, HDA4, HDA5, HDA6 and HDA7 have been identified as histone deacetylases in C. elegans and are homologous with histone deacetylase proteins in both yeast and mammalian systems (2,3). Histone deacetylase HDA1 (also known as Hda1 or N2819 in yeast), deacetylates Histone H2A, H2B, H3 and H4.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
recommended for detection of HDA1 of Saccharomyces cerevisiae origin by WB, IP and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 400-706 mapping at the carboxy terminus of HDA1 of Saccharomyces cerevisiae origin
Tissue Specificity
epitope corresponding to amino acids 400-706 mapping at the carboxy terminus of HDA1 of Saccharomyces cerevisiae origin
Application
Application
Western blot analysis of yeast recombinant Hda1 fusion protein.
Application Notes
recommended for detection of HDA1 of Saccharomyces cerevisiae origin by WB, IP and ELISA:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.