COX-2 (Protein|Antibody|cDNA Clone|ELISA Kit)

All COX-2 reagents are produced in house and quality controlled, including 1 COX-2 Antibody, 14 COX-2 Gene, 1 COX-2 Lysate, 1 COX-2 Protein, 1 COX-2 qPCR. All COX-2 reagents are ready to use.

Recombinant COX-2 proteins are expressed by Baculovirus-Insect Cells with fusion tags as C-His.

COX-2antibodies are validated with different applications, which are IHC-P.

COX-2cDNA clones are full length sequence confirmed and expression validated. There are 13 kinds of tags for each COX-2 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.

COX-2 Protein (1)


COX-2 Protein, Human, Recombinant (His Tag)


Expression host: Baculovirus-Insect Cells

Human COX-2/PTGS2 Protein 9939

COX-2 Antibody (1)


Anti-COX-2 Antibody


Application: IHC-P

Clonality: PAb

Mouse COX-2 Immunohistochemistry(IHC) 19185

COX-2 cDNA Clone (14)


COX-2 qPCR Primer (1)

COX-2 Lysate (1)

PTGS2, also known as COX-2, is s component of Prostaglandin-endoperoxide synthase (PTGS). PTGS, also known as cyclooxygenase, is the key enzyme in prostaglandin biosynthesis, and acts both as a dioxygenase and as a peroxidase. There are two isozymes of PTGS: a constitutive PTGS1 and an inducible PTGS2, which differ in their regulation of expression and tissue distribution. PTGS2 is over expressed in many cancers. The overexpression of PTGS2 along with increased angiogenesis and GLUT-1 expression is significantly associated with gallbladder carcinomas. Furthermore the product of COX-2, PGH2 is converted by prostaglandin E2 synthase into PGE2, which in turn can stimulate cancer progression. Consequently inhibiting COX-2 may have benefit in the prevention and treatment of these types of cancer. PTGS2 is regulated by specific stimulatory events, suggesting that it is responsible for the prostanoid biosynthesis involved in inflammation and mitogenesis. It mediates the formation of prostaglandins from arachidonate and may have a role as a major mediator of inflammation and/or a role for prostanoid signaling in activity-dependent plasticity.

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