Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Myeloperoxidase Protein (MPO) (His tag)

This Recombinant Myeloperoxidase protein is expressed in Human Cells.
Catalog No. ABIN7320799

Quick Overview for Myeloperoxidase Protein (MPO) (His tag) (ABIN7320799)

Target

See all Myeloperoxidase (MPO) Proteins
Myeloperoxidase (MPO)

Protein Type

Recombinant

Origin

  • 12
  • 4
  • 3
  • 2
  • 2
  • 2
Mouse

Source

  • 14
  • 3
  • 2
  • 1
  • 1
Human Cells

Purity

> 90 % as determined by reducing SDS-PAGE.
  • Purification tag / Conjugate

    This Myeloperoxidase protein is labelled with His tag.

    Purpose

    Recombinant Mouse Myeloperoxidase/MPO Protein (His Tag)

    Sequence

    Met16-Thr718

    Characteristics

    Recombinant Mouse Myeloperoxidase is produced by our Mammalian expression system and the target gene encoding Met16-Thr718 is expressed with a 10His tag at the C-terminus.

    Endotoxin Level

    < 1.0 EU per μg as determined by the LAL method.
  • Want other Options for this Protein ?

    !
    Discover Our Predefined Custom Proteins and Custom Protein Services!

    Your project requires further customization? Contact us and discover our custom protein solutions

  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Please refer to the printed manual for detailed information.

    Buffer

    Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Target

    Myeloperoxidase (MPO)

    Alternative Name

    Myeloperoxidase/MPO

    Background

    Background: Myeloperoxidase (MPO) is a hemecontaining enzyme belonging to the XPO subfamily of peroxidases. It is an abundant neutrophil and monocyte glycoprotein that catalyzes the hydrogen peroxidedependent conversion of chloride, bromide, and iodide to multiple reactive species. MPO activity results in protein nitrosylation and the formation of 3-chlorotyrosine and dityrosine crosslinks. Modification of ApoB100, as well as the lipid and cholesterol components of LDL and HDL, promotes the development of atherosclerosis. MPO is also associated with a variety of other diseases, and inhibits vasodilation in inflammation by depleting the levels of NO. Serum albumin functions as a carrier protein during MPO movement to the basolateral side of epithelial cells. MPO is stored in neutrophil azurophilic granules. Upon cellular activation, it is deposited into pathogencontaining phagosomes. While mice lacking MPO are impaired in clearing select microbial infections,MPO deficiency in humans does not necessarily result in heightened susceptibility to infections.

    Synonym: Myeloperoxidase, MPO

    Molecular Weight

    81.1 kDa

    UniProt

    P11247

    Pathways

    Chromatin Binding
You are here:
Chat with us!