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Complement Factor H Antikörper

Dieses Maus Monoklonal-Antikörper erkennt spezifisch Complement Factor H in WB, FACS und IA. Er zeigt eine Reaktivität gegenüber Maus.
Produktnummer ABIN2191858

Kurzübersicht für Complement Factor H Antikörper (ABIN2191858)

Target

Alle Complement Factor H (CFH) Antikörper anzeigen
Complement Factor H (CFH)

Reaktivität

  • 79
  • 15
  • 13
  • 3
  • 2
Maus

Wirt

  • 64
  • 32
  • 3
  • 2
Maus

Klonalität

  • 60
  • 40
  • 1
Monoklonal

Konjugat

  • 64
  • 12
  • 7
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Dieser Complement Factor H Antikörper ist unkonjugiert

Applikation

  • 78
  • 49
  • 32
  • 32
  • 26
  • 17
  • 13
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunoassay (IA)

Klon

1A2
  • Kreuzreaktivität (Details)

    Cross reactivity: (Yes/No) Rat : Yes

    Sterilität

    0.2 μm filtered

    Isotyp

    IgG1
  • Applikationshinweise

    For immunohistology and Western blotting, 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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS, containing 0.1 % 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 one year.

    Haltbarkeit

    12 months
  • Target

    Complement Factor H (CFH)

    Andere Bezeichnung

    Factor H

    Hintergrund

    Monoclonal antibody 1A2 recognizes mouse complement factor H (CFH). CFH is the first regulatory protein of the alternative pathway of the complement system. There are three pathways of complement activation, classical, alternative, and lectin activation pathway. These pathways converge to form C3/C5 convertases that generate C3a, C3b,C5a, and C5b, each with substantial biologic activity. Complement regulators are necessary to prevent the injudicious production of these mediators and potential injury to self-tissue. The plasma proteins CFH, C4-binding protein and the cell membrane proteins complement receptor 1 (CR1, CD35), decay-accelerating factor (CD55), and membrane co-factor protein (CD46) all are members of the regulators of complement activation family. These proteins have natural affinity for C3b and/or C4b, which confers on them the ability to accelerate the intrinsic decay of C3/C5 convertases and/or act as co-factor for the cleavage and inactivation (i) of C3b and C4b by complement factor I (CFI). Genetic human analyses reveals a clear association of CFH with different human diseases. These include diseases of the kidney, the atypical form of Hemolytic Uremic Syndrome (aHUS) and membranoproliferative glomerulonephritis (MPGN). Furthermore, CFH is associated with age-related macular degeneration (AMD), a disease of the eye. Immunogen Mouse factor H-human IgG fusion protein

    Pathways

    Komplementsystem, Cellular Response to Molecule of Bacterial Origin
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