recommended for detection of PARG of human origin by WB, IF, IHC(P) and ELISA
Modification Notes
The synthesis and rapid turnover of ADP-ribose polymers is an immediate cellular response to DNA damage. Poly (ADP-ribose) is a reversible covalent-modifier to chromosomal proteins and is synthesized by poly (ADP-ribose) polymerase (PARP-1) and other related enzymes. Poly (ADP-ribose) glycohydrolase (PARG) is the enzyme responsible for polymer turnover. Under normal growth conditions, PARG localizes to the cytoplasm. PARG is an enzymatically active protein that is cleaved to multiple fragments. PARG is cleaved during etoposide-, staurosporine-, and Fas-induced apoptosis in human cells by caspases, and generates two C-terminal fragments, which still contain the active site of the enzyme required to hydrolyze poly (ADP-ribose). Under normal growth, PARG is expressed only as a doublet by SDS-PAGE. The gene encoding PARG maps to human chromosome 10q11.23.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIFIHCELISA
WB:1:500~1:2000 IF:1:200~1:500 IHC:1:50~1:200 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 PARG of human origin by WB IF IHC(P) and ELISA
Tissue Specificity
recommended for detection of PARG of human origin by WB, IF, IHC(P) and ELISA