Recombinant Human HRAS Protein

Cat.No. : HRAS-2135H
Product Overview : Recombinant wild-type human HRAS protein without tag was expressed in E. coli.
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Species : Human
Source : E.coli
Description : This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, cognitive disability, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in this gene are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma. Multiple transcript variants, which encode different isoforms, have been identified for this gene.
Form : Liquid
Purity : ≥ 95% (SDS-PAGE)
Storage : At -80 centigrade.
Storage Buffer : In 20mM TRIS-HCl, pH 8.0, containing 45mM sodium chloride, 1mM DTT, 5mM magnesium chloride and 50% glycerol.
Shipping : Dry Ice
Gene Name HRAS HRas proto-oncogene, GTPase [ Homo sapiens (human) ]
Official Symbol HRAS
Synonyms HRAS; HRas proto-oncogene, GTPase; CTLO; HAMSV; HRAS1; RASH1; p21ras; C-H-RAS; H-RASIDX; C-BAS/HAS; C-HA-RAS1; GTPase HRas; GTP- and GDP-binding peptide B; Ha-Ras1 proto-oncoprotein; Harvey rat sarcoma viral oncogene homolog; Harvey rat sarcoma viral oncoprotein; Ras family small GTP binding protein H-Ras; c-has/bas p21 protein; p19 H-RasIDX protein; transformation gene: oncogene HAMSV; transforming protein p21; v-Ha-ras Harvey rat sarcoma viral oncogene homolog; EC 3.6.5.2
Gene ID 3265
mRNA Refseq NM_176795
Protein Refseq NP_789765
MIM 190020
UniProt ID P01112

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