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- mouse monoclonal IgG1; 100 µg/ml
- raised against a recombinant protein
- recommended for detection of H-Ras p21 of mouse, rat and human origin by WB, IP, IF and IHC(P)
- does not block binding of H-Ras to Raf
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H-Ras Background Information The mammalian Ras (also designated v-Ha-Ras, Harvey rat sarcoma viral oncogene homolog, HRAS1, K-Ras, N-Ras, RASH1 or c-bas/has) gene family consists of the Harvey and Kirsten Ras genes (c-H-Ras1 and c-K-Ras2), an inactive pseudogene of each (c-H-Ras2 and c-K-Ras1) and the N-Ras gene. The three Ras oncogenes, H-Ras, K-Ras and N-Ras, encode proteins with GTP/GDP binding and GTPase activity. Ras proteins alternate between an inactive form bound to GDP and an active form bound to GTP, activated by a guanine nucleotide-exchange factor (GEF) and inactivated by a GTPase-activating protein (GAP). Ras nomenclature originates from the characterization of human DNA sequences homologous to cloned DNA fragments containing oncogenic sequences of a type C mammalian retrovirus, the Harvey strain of murine sarcoma virus (HaMSV), derived from the rat. Under normal conditions, Ras family members influence cell growth and differentiation events in a subcellular membrane compartmentalization-based signaling system. Oncogenic Ras can deregulate processes that control both cell proliferation and apoptosis. The Ras superfamily of GTP hydrolysis-coupled signal transduction relay proteins can be subclassified into Ras, Rho, Rab and ARF families.
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See how others have used H-Ras (F235): sc-29 antibody and or H-Ras (F235) antibody conjugates.
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H-Ras (F235)
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H-Ras (F235): sc-29. Immunoperoxidase staining of formalin fixed, paraffin-embedded mouse colon tissue showing cytoplasmic localization.
H-Ras (F235): sc-29. Western blot analysis of human recombinant H-Ras fusion protein.
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