epitope corresponding to amino acids 33-119 mapping near the N-terminus (Ce)
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 (1). 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). RBA1 and RBA2 are the C. elegans homologues of RbAp46 and RBAp48 respectively. RbAp46 and RbAp48 are Rb and histone binding proteins and are components of the histone deacetylase complex (4-6).
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of HDA7 of Caenorhabditis elegans origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 33-119 mapping near the N-terminus (Ce)
Tissue Specificity
epitope corresponding to amino acids 33-119 mapping near the N-terminus (Ce)
Application
Application
Western blot analysis of C. elegans recombinant HDA7 fusion protein.
Application Notes
recommended for detection of HDA7 of Caenorhabditis elegans origin by WB, IP, IF 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.