PTGS2 anticorps (N-Term)

N° du produit ABIN965923

Détail du produit anti-PTGS2 anticorps

Antigène: PTGS2 (Prostaglandin-Endoperoxide Synthase 2 (Prostaglandin G/H Synthase and Cyclooxygenase) (PTGS2))

Épitope: N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PTGS2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Souris, Rat (Rattus)

Réactivité croisée (Details): No cross reactivity with other proteins.

Attributs du produit: Rabbit IgG polyclonal antibody for Prostaglandin G/H synthase 2 (PTGS2) detection. Tested with WB, IHC-P in Human, Mouse, Rat.

Immunogène: A synthetic peptide corresponding to a sequence at the N-terminal of human COX-2, different from the related rat sequence by two amino acids.< br/>Immunogen was affinity purified.

Isotype: IgG

Information d'application

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 0.2 mL of distilled water will yield a concentration of 500 µg/mL.

Buffer: Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Thimerosal, 0.05 mg Sodium azide.

Agent conservateur: Sodium azide, Thimerosal (Merthiolate)

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: -20 °C

Stockage commentaire: At -20 °C for one year. After reconstitution, at 4 °C for one month. It can also be aliquotted and stored frozen at -20 °C for a longer time.

Références pour anticorps anti-PTGS2 (ABIN965923)

Wilkinson-Berka, Alousis, Kelly, Gilbert: "COX-2 inhibition and retinal angiogenesis in a mouse model of retinopathy of prematurity." dans: Investigative ophthalmology & visual science, Vol. 44, Issue 3, pp. 974-9, (2003) (PubMed).

Brewer, Khor, Vogt, Muglia, Fujiwara, Haegele, Sleckman, Muglia: "T-cell glucocorticoid receptor is required to suppress COX-2-mediated lethal immune activation." dans: Nature medicine, Vol. 9, Issue 10, pp. 1318-22, (2003) (PubMed).

Liu, Chang, Narko, Trifan, Wu, Smith, Haudenschild, Lane, Hla: "Overexpression of cyclooxygenase-2 is sufficient to induce tumorigenesis in transgenic mice." dans: The Journal of biological chemistry, Vol. 276, Issue 21, pp. 18563-9, (2001) (PubMed).

Détails sur PTGS2

Antigène: PTGS2 (Prostaglandin-Endoperoxide Synthase 2 (Prostaglandin G/H Synthase and Cyclooxygenase) (PTGS2))

Autre désignation: Prostaglandin G/H synthase 2 (PTGS2 Produits)

Synonymes: anticorps COX-2, anticorps COX2, anticorps GRIPGHS, anticorps PGG/HS, anticorps PGHS-2, anticorps PHS-2, anticorps hCox-2, anticorps Cox-2, anticorps Pghs2, anticorps TIS10, anticorps Cox2, anticorps cox-2, anticorps CEF147, anticorps PGHS2, anticorps PHSII, anticorps cox2, anticorps gripghs, anticorps pgg/hs, anticorps pghs-2, anticorps phs-2, anticorps PTGS2, anticorps hcox-2, anticorps fj02a10, anticorps ptgs2, anticorps unp1239, anticorps wu:fj02a10, anticorps zCOX-2, anticorps si:dkey-97o5.6, anticorps prostaglandin-endoperoxide synthase 2, anticorps prostaglandin G/H synthase 2, anticorps prostaglandin-endoperoxide synthase 2S homeolog, anticorps prostaglandin-endoperoxide synthase 2a, anticorps prostaglandin-endoperoxide synthase 2b, anticorps PTGS2, anticorps Ptgs2, anticorps LOC100136456, anticorps ptgs2.S, anticorps ptgs2, anticorps ptgs2a, anticorps ptgs2b

Sujet: Cyclooxygenase (Cox) is the key enzyme in conversion of arachidonic acid to PGs, and two isoforms, Cox-1 and Cox-2, have been identified. Cox-2 gene encodes an inducible prostaglandin synthase enzyme that is overexpressed in adenocarcinomas and other tumors. Deletion of the murine Cox-2 gene in Min mice reduced the incidence of intestinal tumors, suggesting that it is required for tumorigenesis. This gene is localized to sites associated with retinal blood vessels, and plays an important role in blood vessel formation in the retina. And the glucocorticoid receptor suppression of COX-2 is also crucial for curtailing lethal immune activation, and suggest new therapeutic approaches for regulation of T-cell-mediated inflammatory diseases.

Pathways: Brown Fat Cell Differentiation, Positive Regulation of fat Cell Differentiation