recommended for detection of M-Ras of human origin by WB, IP and ELISA
Modification Notes
The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode proteins that are ubiquitously expressed in vertebrate cells. c-H- and c-K-Ras are cellular homologs of the v-H- and v-K-Ras sequences originally isolated from the Harvey and Kirsten strains of rat sarcoma virus. p21Ras-encoded proteins bind GDP and GTP with high affinity and possess a low level intrinsic GTPase activity that can be stimulated over 100-fold by interaction with cytosolic GTPase activating protein (GAP), a potential effector for Ras p21 function. Point mutations at amino acids 12, 13, 59 and 61 within domains responsible for GTP binding and hydrolysis activate Ras proteins to their oncogenic form and block the ability of their GTPase activities to be stimulated by GAP. M-Ras has been identified as a GTPase that shares structural similarities to the Ras family proteins. M-Ras is thought to play a role in reorganization of the actin cytoskeleton.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
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 M-Ras of human origin by WB IP and ELISA
Tissue Specificity
recommended for detection of M-Ras of human origin by WB, IP and ELISA