BD-PT2960

N/H/K-Ras Rabbit Polyclonal Antibody

NRAS; HRAS1; GTPase NRas; Transforming protein N-Ras; HRAS; HRAS1; GTPase HRas; H-Ras-1; Ha-Ras; Transforming protein p21; c-H-ras; p21ras; KRAS; KRAS2; RASK2; GTPase KRas; K-Ras 2; Ki-Ras; c-K-ras; c-Ki-ras

常规抗体

NRAS/HRAS/KRAS

GTPase Nras/GTPase Hras/GTPase Kras

WB

Human,Mouse,Rat

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

3265/3845/4893

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=3265

P01111/P01112/P01116

http://www.uniprot.org/uniprotkb/P01111/entry

15461/16653

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=15461

24605/293621/24525

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=24605

Q04970/P20171/P08644

http://www.uniprot.org/uniprot/Q04970

The antiserum was produced against synthesized peptide derived from human RASH/RASK. AA range:1-50

N/H/K-Ras Polyclonal Antibody detects endogenous levels of N/H/K-Ras protein.

WB 1:500 - 1:2000. IHC-p: 1:100-300 ELISA: 1:20000. IF 1:100-300 Not yet tested in other applications.

21kD

-20°C/1 year

Polyclonal, Rabbit,IgG

This is an N-ras oncogene encoding a membrane protein that shuttles between the Golgi apparatus and the plasma membrane. This shuttling is regulated through palmitoylation and depalmitoylation by the ZDHHC9-GOLGA7 complex. The encoded protein, which has intrinsic GTPase activity, is activated by a guanine nucleotide-exchange factor and inactivated by a GTPase activating protein. Mutations in this gene have been associated with somatic rectal cancer, follicular thyroid cancer, autoimmune lymphoproliferative syndrome, Noonan syndrome, and juvenile myelomonocytic leukemia. [provided by RefSeq, Jun 2011],

Bone marrow,Bone-marrow,Brain,Fibrosarcoma,Kidney,Leukemia,Lung car

Cell membrane ; Lipid-anchor ; Cytoplasmic side . Golgi apparatus membrane ; Lipid-anchor . Shuttles between the plasma membrane and the Golgi apparatus. .

MAPK_ERK_Growth;MAPK_G_Protein;ErbB_HER;Chemokine;Axon guidance;VEGF;Tight junction;Gap junction;Natural killer cell mediated cytotoxicity;T_Cell_Receptor;B_Cell_Antigen;Fc epsilon RI;Long-term potentiation;Neurotrophin;Long-term depression;Regulates Acti

disease:Defects in NRAS are a cause of juvenile myelomonocytic leukemia (JMML) [MIM:607785]. JMML is a pediatric myelodysplastic syndrome that constitutes approximately 30% of childhood cases of myelodysplastic syndrome (MDS) and 2% of leukemia.,disease:Mutations which change AA 12, 13 or 61 activate the potential of Ras to transform cultured cells and are implicated in a variety of human tumors.,enzyme regulation: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).,function:Ras proteins bind GDP/GTP and possess intrinsic GTPase activity.,online information:NRAS mutation db,online information:RAS proteins entry,PTM:Palmitoylated by the ZDHHC9-GOLGA7 complex. A continuous cycle of de- and re-palmitoylation regulates rapid exchange between plasma membrane and Golgi.,similarity:Belongs to the small GTPase superfamily. Ras family.,subcellular location:Shuttles between the plasma membrane and the Golgi apparatus.,

现货

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.