H-Ras

Harvey rat sarcoma viral oncogene homolog

human, recombinant, E. coli

Catálogo Nº Apresentação Preço (R$) Comprar / Observação
PR-107 50 μg Sob demanda Adicionar ao Carrinho

For general laboratory use.

Envio: shipped on dry ice

Condições de armazenamento: store at -80 °C
avoid freeze/thaw cycles

Validade: 12 months

Peso molecular: 21.3 kDa (189 amino acids)

Número de acesso: NP_005334

Número de acesso: NP_005334

Pureza: > 90 % (SDS-PAGE)

Forma: liquid (Supplied in 25 mM HEPES pH 7.2, 40 mM NaCl, 3 mM DTT, 2 mM MgCl2 and 0.01 mM GDP)

Atividade: GTPγS binding: >750 mmol/mol.

Descrição:
Ras proteins are members of the superfamily of small GTP-binding proteins that function as molecular switches controlling a variety of signaling and transport pathways. H-Ras is one of the classic human Ras proteins (H-, N-, K-Ras4A, and K-Ras4B). Suitable as a substrate for farnesyltransferase. Protein preparation is 98% GDP- and 2% GTP-loaded, measured by HPLC.

Referências selecionadas:
Sasazuki et al. (2005) Transformation by Oncogenic RAS Sensitizes Human Colon Cells to TRAIL-induced Apoptosis by Up-regulating Death Receptor 4 and Death Receptor 5 through a MEK-dependent Pathway. J Biol. Chem. 280:22856. Marshall (1995) Ras target proteins in eukaryotic cells. FASEB J. 9:1311. Reiss et al. (1990) Inhibition of purified p21ras farnesyl-protein transferase by Cys-aaX tetrapeptides. Cell 62:81. Chaussade et al. (2009) Functional differences between two classes of oncogenic mutation in the PIK3CA gene. Biochemical and Biophysical Research Communications 381 (4):577-581.