epitope mapping within a C-terminal cytoplasmic domain of MRGF of human origin
Modification Notes
MRGF (MAS-related GPR, member F), also known as RTA, PSEC0142, GPR140 (G-protein coupled receptor 140) or GPR168 (G-protein coupled receptor 168), is a 343 amino acid multi-pass membrane protein that functions as an orphan receptor. MRGF belongs to the G-protein coupled receptor 1 family and Mas subfamily, and is thought to have a role in pain sensation and modulation by regulating nociceptor function. The gene encoding MRGF maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of MRGF of mouse, rat and human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within a C-terminal cytoplasmic domain of MRGF of human origin
Tissue Specificity
epitope mapping within a C-terminal cytoplasmic domain of MRGF of human origin