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Myeloperoxidase Antikörper (FITC)

Der Maus Monoklonal Anti-Myeloperoxidase-Antikörper wurde für IA validiert. Er ist geeignet, Myeloperoxidase in Proben von Maus zu detektieren. Es sind 4+ Publikationen verfügbar.
Produktnummer ABIN2191799

Kurzübersicht für Myeloperoxidase Antikörper (FITC) (ABIN2191799)

Target

Alle Myeloperoxidase (MPO) Antikörper anzeigen
Myeloperoxidase (MPO)

Reaktivität

  • 186
  • 65
  • 58
  • 8
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
Maus

Wirt

  • 147
  • 91
  • 1
  • 1
  • 1
Maus

Klonalität

  • 134
  • 107
Monoklonal

Konjugat

  • 125
  • 29
  • 28
  • 10
  • 9
  • 9
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Myeloperoxidase Antikörper ist konjugiert mit FITC

Applikation

  • 146
  • 94
  • 88
  • 60
  • 56
  • 52
  • 36
  • 20
  • 16
  • 14
  • 14
  • 13
  • 10
  • 7
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Immunoassay (IA)

Klon

8F4
  • Kreuzreaktivität (Details)

    Cross reactivity: Rat MPO : Yes

    Sterilität

    0.2 μm filtered

    Isotyp

    IgG1
  • Applikationshinweise

    For immunohistochemistry and flow cytometry, dilutions to be used depend on detection system applied. It is recommended that users test the reagent and determine their own optimal dilutions. The typical starting working dilution is 1:50 Positive Neutrophils isolated from digested infarcts control 1

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS, containing 1 % bovine serum albumin and 0.02 % sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C

    Informationen zur Lagerung

    Product should be stored at 4 °C. Under recommended storage conditions, product is stable for at least one year. The exact expiry date is indicated on the label.
  • Matthijsen, Huugen, Hoebers, de Vries, Peutz-Kootstra, Aratani, Daha, Tervaert, Buurman, Heeringa: "Myeloperoxidase is critically involved in the induction of organ damage after renal ischemia reperfusion." in: The American journal of pathology, Vol. 171, Issue 6, pp. 1743-52, (2007) (PubMed).

    van Leeuwen, Gijbels, Duijvestijn, Smook, van de Gaar, Heeringa, de Winther, Tervaert: "Accumulation of myeloperoxidase-positive neutrophils in atherosclerotic lesions in LDLR-/- mice." in: Arteriosclerosis, thrombosis, and vascular biology, Vol. 28, Issue 1, pp. 84-9, (2007) (PubMed).

    Wang, DCosta, Civin, Friedman: "C/EBPalpha directs monocytic commitment of primary myeloid progenitors." in: Blood, Vol. 108, Issue 4, pp. 1223-9, (2006) (PubMed).

    Huugen, Xiao, van Esch, Falk, Peutz-Kootstra, Buurman, Tervaert, Jennette, Heeringa: "Aggravation of anti-myeloperoxidase antibody-induced glomerulonephritis by bacterial lipopolysaccharide: role of tumor necrosis factor-alpha." in: The American journal of pathology, Vol. 167, Issue 1, pp. 47-58, (2005) (PubMed).

  • Target

    Myeloperoxidase (MPO)

    Andere Bezeichnung

    Myeloperoxidase

    Hintergrund

    The monoclonal antibody 8F4 recognizes mouse myeloperoxidase (MPO). MPO is a glycoprotein produced as a single precursor, which is subsequently cleaved into a alpha and beta chain. In human the biologically active MPO is a 150 kDa tetramer composed of 2 glycosylated alfa chains of 59-64 kDa and 2 beta chains of 14 kDa. MPO is stored in azurophilic granules of polymorphonuclear leukocytes and is rapidly released into the phagosome and extracellular space during inflammatory conditions.The enzyme catalyzes the conversion of chloride and hydrogen peroxide to hypochlorite, a potent oxidant, which functions in host defense against microorganisms. Involvement of MPO has been described in several human diseases, such as cardiovascular disease, airway inflammation, lung cancer, Alzheimer's disease and multiple sclerosis. A positive correlation between elevated MPO levels in serum and cardiovascular disease suggest an interesting role for MPO as an diagnostic marker, making it possible to identify patients at risk for future cardiac events. Furthermore, there are some autoimmune diseases, in which MPO is targeted by antineutrophil cytoplasm antibodies. Studies with MPO-knockout mice have shown an increased susceptibility to pneumonia following intratracheal infections. Moreover, MPO deficient mice are more susceptible to experimental autoimmune encephalitis, a T cell-dependent neuronal disease, and have an increased expression of arteriosclerotic plaques compared to wild-type mice. The anti-mouse MPO monoclonal antibody 8F4 recognizes natural MPO in biological solutions by ELISA, in frozen tissue sections fixed with acetone and in flow cytometry using a cell permeabilization method. The antibody 8F4 is cross-reactive with rat MPO. Immunogen Purified mouse MPO from WEHI-3 cells

    Pathways

    Chromatin Binding
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