Anti-SerpinA3 antibody

Cat.#: 102465

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Product Information

  • Product Name
    Anti-SerpinA3 antibody
  • Documents
  • Description
    Rabbit polyclonal to SerpinA3
  • Tested applications
    ELISA, WB
  • Species reactivity
    Human SerpinA3 / AACT
  • Alternative names
    AACT antibody; ACT antibody; alpha-1-antichymotrypsin antibody; GIG24 antibody; GIG25 antibody; MGC88254 antibody; SERPINA3 antibody
  • Immunogen
  • Isotype
    Rabbit IgG
  • Preparation
    Produced in rabbits immunized with purified, recombinant Human SerpinA3 (rh SerpinA3; NP_001076.2; Met 1-Ala 423). SerpinA3 specific IgG was purified by human SerpinA3 affinity chromatography.
  • Clonality
    Polyclonal
  • Formulation
    0.2 μm filtered solution in PBS with 5% trehalose
  • Storage instructions
    This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free.
    Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.
  • Applications

    WB: 5-10 μg/mL

    ELISA: 0.5-1 μg/mL

    This antibody can be used at 0.5-1 μg/mL with the appropriate secondary reagents to detect Human SERPINA3. The detection limit for Human SERPINA3 is approximately 0.0049 ng/well.

  • Validations

    SerpinA3 / AACT Antibody, Rabbit PAb, Antigen Affinity Purified, Western blot

    SerpinA3 / AACT Antibody, Rabbit PAb, Antigen Affinity Purified, Western blot

  • Background
    Human SerpinA3, also known as Alpha 1-antichymotrypsin (AACT), is a plasma alpha globulin glycoprotein, and is a member of serpin superfamily of the serine protease inhibitors consisting of at least 35 members. SerpinA3 has been demonstrated to inhibit the activity of certain serine proteases, such as cathepsin G found in neutrophils, and chymases present in mast cells, by inducing a major conformational rearrangement, and thus protects some tissues from damage caused by proteolytic enzymes. This enzyme is produced primarily in the liver, and is identified as an acute-phase inflammatory protein. SerpinA3 deficiency has been associated with liver disease, and mutations of this gene have been observed in patients with Parkinson disease and chronic obstructive pulmonary disease. In addition, ACT gene polymorphism has been implicated with Alzheimer’s disease (AD), cerebral amyloid angiopathy (CAA), as well as stroke, since SerpinA3 is a major constituent of the plaques in AD and an inhibitor of amyloid beta peptide degradation.
  • References
    • Nilsson, L.N. et al., 2001, J. Neurosci. 21: 1444-1451.
    • Ikari, Y. et al., 2001, J. Biol. Chem. 276: 11798-11803.
    • Vila, N. et al., 2000, Stroke. 31: 2103-2105
    • Eriksson, S. et al., 1995, Proc. Natl. Acad. Sci. USA. 92: 2313-2317.
    • Skeel, A. et al., 2001, J. Biol. Chem. 276: 21932-21937.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"