KRAS (Protein|Antibody|cDNA Clone|ELISA Kit)

All KRAS reagents are produced in house and quality controlled, including 3 KRAS Antibody, 26 KRAS Gene, 3 KRAS Protein, 1 KRAS qPCR. All KRAS reagents are ready to use.

Recombinant KRAS proteins are expressed by E. coli with fusion tags as N-His.

KRAS antibodies are validated with different applications, which are ELISA, WB, IHC-P.

KRAS cDNA clones are full length sequence confirmed and expression validated. There are 13 kinds of tags for each KRAS of different species, especially GFP tag, OFP tag, FLAG tag and so on. There are three kinds of vectors for choice, cloning vector, expression vector and lentivrial expression vector.

KRAS Protein (3)


KRAS Protein, Human, Recombinant (His Tag)


Expression host: E. coli

Human KRAS/K-RAS Protein 10023

KRAS Protein, Human, Recombinant (12 Asp, His Tag)


Expression host: E. coli

Human KRAS/K-RAS Protein 10024

KRAS Protein, Human, Recombinant (12 Cys, His Tag)


Expression host: E. coli

Human KRAS/K-RAS Protein 10025

KRAS Antibody (3)

Application Clonality

Anti-KRAS Antibody


Specificity: Human

Application: ELISA

Clonality: PAb

Anti-KRAS Antibody


Application: WB,IHC-P

Clonality: PAb

Human KRAS Western blot (WB) 22275

Anti-KRAS Antibody


Specificity: Human

Application: WB

Clonality: PAb

Human KRAS/K-RAS Western blot (WB) 6914

KRAS cDNA Clone (26)


KRAS qPCR Primer (1)

K-Ras belongs to the small GTPase superfamily, Ras family. As other members of the Ras family, K-Ras is a GTPase and is an early player in many signal transduction pathways. It is usually tethered to cell membranes because of the presence of an isoprenyl group on its C-terminus. K-Ras functions as a molecular on/off switch. Once it is turned on it recruits and activates proteins necessary for the propagation of growth factor and other receptors' signal, such as c-Raf and PI 3-kinase. It binds to GTP in the active state and possesses an intrinsic enzymatic activity which cleaves the terminal phosphate of the nucleotide converting it to GDP. Upon conversion of GTP to GDP, K-Ras is turned off. The rate of conversion is usually slow but can be sped up dramatically by an accessory protein of the GTPase activating protein class, for example RasGAP. In turn K-Ras can bind to proteins of the Guanine Nucleotide Exchange Factor class, for example SOS1, which forces the release of bound nucleotide. Subsequently, K-Ras binds GTP present in the cytosol and the GEF is released from ras-GTP. Besides essential function in normal tissue signaling, the mutation of a K-Ras gene is an essential step in the development of many cancers. Several germline K-Ras mutations have been found to be associated with Noonan syndrome[4] and cardio-facio-cutaneous syndrome. Somatic K-Ras mutations are found at high rates in Leukemias, colon cancer, pancreatic cancer and lung cancer.Immune Checkpoint   Immunotherapy   Cancer Immunotherapy   Targeted Therapy