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Complement Factor H anticorps

L’anticorps Lapin Polyclonal anti-Complement Factor H a été validé pour ELISA. Il convient pour détecter Complement Factor H dans des échantillons de Humain.
N° du produit ABIN7670580

Aperçu rapide pour Complement Factor H anticorps (ABIN7670580)

Antigène

Voir toutes Complement Factor H (CFH) Anticorps
Complement Factor H (CFH)

Reactivité

  • 71
  • 12
  • 12
  • 2
  • 2
Humain

Hôte

  • 56
  • 27
  • 3
  • 2
Lapin

Clonalité

  • 52
  • 35
  • 1
Polyclonal

Conjugué

  • 54
  • 10
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp Complement Factor H est non-conjugé

Application

  • 65
  • 35
  • 25
  • 22
  • 19
  • 16
  • 13
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
ELISA
  • Fonction

    Complement Factor H/CFH Polyclonal Antibody(Capture/Detector)

    Purification

    Antigen Affinity Purification

    Immunogène

    Recombinant Human Complement Factor H/CFH protein expressed by Mammalian

    Isotype

    IgG
  • Indications d'application

    ELISA Capture 2-8 μg/mL,ELISA Detector 0.1-0.4 μg/mL

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Sterile PBS , pH 7.4

    Agent conservateur

    Without preservative

    Conseil sur la manipulation

    Avoid freeze / thaw cycles. This preparation contains no preservatives, thus it should be handled under aseptic conditions.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C Valid for 1 month or -20°C Valid for 12 months

    Date de péremption

    12 months
  • Antigène

    Complement Factor H (CFH)

    Autre désignation

    Complement Factor H/CFH

    Sujet

    CF-H,AHUS1,AMBP1,FH,FHL1,ARMD4,ARMS1,CFHL3,HF,HF1,HF2,HUS,Complement factor H (CFH) is an abundant plasma glycoprotein that regulates the function of the alternative complement pathway in fluid phase and on cellular surfaces. Factor H binds to C3b,accelerates the decay of the alternative pathway C3-convertase (C3bBb) and acts as a cofactor for the factor I-mediated proteolytic inactivation of C3b. It plays a critical role in the homeostasis of the complement system in plasma and in the protection of bystander host cells and tissues from damage by complement activation. Abnormalities in factor H have been associated with renal disease.

    UniProt

    P08603

    Pathways

    Système du Complément, Cellular Response to Molecule of Bacterial Origin
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