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Anti-Complement Factor H Antibody ELISA Kit

This Colorimetric ELISA kit is designed for the quantitative measurement of Human .
Catalog No. ABIN459353

Quick Overview for Anti-Complement Factor H Antibody ELISA Kit (ABIN459353)

Target

Anti-Complement Factor H Antibody

Reactivity

Human

Detection Method

Colorimetric

Method Type

Indirect ELISA

Application

ELISA

Sample Type

Serum, Plasma
  • Purpose

    anti-complement factor H is an enzyme linked immunosorbent assay designed to detect IgG antibodies against complement factor H.

    Brand

    ELISA-VIDITEST

    Analytical Method

    Quantitative

    Components

    • ELISA strips coated with human factor H purified from human plasma STRIPS Ag 1 x 6 strips
    • 50 μL Anti-CFH IgG standard STANDARD 1 vial
    • 0.1 mL IgG-HRP conjugate - detection anti-human antibody labelled by horseradish peroxidase,101x concentrated CONJ 101x 1 vial
    • 55 mL Wash buffer 10x concentrated WASH 10x 1 vial
    • 60 mL Dilution buffer (DB) r.t.u. 1) DIL 1 vial
    • 13 mL Chromogenic substrate (TMB-BF substrate) r.t.u. (TMB/H2O2) TMB-BF 1 vial
    • 13 mL Stop solution r.t.u. (0.4 M sulfuric acid) STOP 1 vial
    • Instruction manual
    • Quality control certificate 1) r.t.u. ready to use

    Material not included

    • Distilled or deionised water for dilution of buffer and standard concentrates
    • appropriate and calibrated equipment for pipetting
    • temperature controlled incubator
    • spectrophotometer or platereader with the appropriate filters
    • empty microtiter plate for pre-incubation
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Plate

    Pre-coated

    Protocol

    anti-complement factor H is an enzyme linked immunosorbent assay designed to detect IgG antibodies against complement factor H. The wells of the microtitrate plate are coated with purified human complement factor H. Antibodies against factor H present in serum sample bind to the immobilized factor H. Other antibodies, unbound to the factor H, are washed away during the next step. Then anti-human IgG antibodies labelled with horseradish peroxidase are added and those detect the antibodies from the sample that previously bound to factor H. The unbound labelled antibodies are washed away and the remaining labelled antibodies are visualized with a chromogenic substrate. The peroxidase activity leads to a change in colour of the solution. The reaction is stopped by adding an acidic solution. The colour intensity is directly proportional to the amount of anti-factor H antibodies in the sample.

    Restrictions

    For Research Use only
  • Storage

    4 °C
  • Target

    Anti-Complement Factor H Antibody

    Target Type

    Antibody
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