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        COX1/Cyclooxygenase 1 Rabbit pAb
        EA023
        規(guī)格: 價(jià)格:
        50μL ¥1280.00
        100μL ¥1980.00

        Overview

        Product name: COX1/Cyclooxygenase 1 Rabbit pAb
        Reactivity: Human
        Source: Rabbit
        Dilutions: WB 1:1,000 IHC 1:100
        Immunogen: Synthetic Peptide
        Storage: PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid?repeated?freeze-thaw?cycles.
        Clonality: Polyclonal
        Isotype: IgG
        Concentration: 1mg/mL
        Observed Band: 70kDa
        GeneID: 5742
        Human Swiss-Prot No: P23219
        Cellular localization: Endoplasmic reticulum, Membrane, Microsome
        Background: Cyclooxygenase-1 (COX-1), also known as prostaglandin G/H synthase 1, prostaglandin-endoperoxide synthase 1 or prostaglandin H2 synthase 1, is an enzyme that in humans is encoded by the PTGS1 gene. There are two isozymes of COX encoded by distinct gene products: a constitutive COX-1 (this enzyme) and an inducible COX-2, which differ in their regulation of expression and tissue distribution. The expression of these two transcripts is differentially regulated by relevant cytokines and growth factors. A splice variant of COX-1 termed COX-3 was identified in the CNS of dogs, but does not result in a functional protein in humans. Two smaller COX-1-derived proteins (the partial COX-1 proteins PCOX-1A and PCOX-1B) have also been discovered, but their precise roles are yet to be describedGalectin 3 is one of the more extensively studied members of this family and is a 30 kDa protein. Due to a C-terminal carbohydrate binding site, Galectin 3 is capable of binding IgE and mammalian cell surfaces only when homodimerized or homooligomerized. Galectin 3 is normally distributed in epithelia of many organs, in various inflammatory cells, including macrophages, as well as dendritic cells and Kupffer cells. The expression of this lectin is up-regulated during inflammation, cell proliferation, cell differentiation and through trans-activation by viral proteins.
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