Tick-Borne Encephalitis Virus IgG and IgG Avidity ELISA 试剂盒
This 人 ELISA Kit is a Colorimetric ELISA Kit designed to quantify 人 .
Quick Overview for Tick-Borne Encephalitis Virus IgG and IgG Avidity ELISA 试剂盒 (ABIN459372)
抗原
Tick-Borne Encephalitis Virus IgG and IgG Avidity
适用
人
检测方法
Colorimetric
实验类型
Indirect ELISA
应用范围
ELISA
样品类型
Serum, Plasma
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原理
- anti-TBEV IgG and IgG avidity is a solid-phase immunoanalytical test.
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品牌
- ELISA-VIDITEST
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Analytical Method
- Semi-Quantitative
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组件
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- ELISA break-away strips in the handling frame coated with the specific antigen STRIPS Ag 1 x 12 pcs
- 1.3 mL of positive control human serum containing high avidity antibodies (High avidity control serum) r.t.u.1) HIGH AVID 1 vial
- 1.3 mL of positive control human serum containing low avidity antibodies (Low avidity control serum) r.t.u. LOW AVID 1 vial
- 1.3 mL Standard A = Negative control human serum, r.t.u. ST A/NC 1 vial
- 2.0 mL Standard D = Calibrator (human serum), r.t.u. ST D/CAL 1 vial
- / 1.3 mL Standard E = Positive control human serum, r.t.u. ST E/PC 1 vial
- 13 mL Anti-human IgG animal antibodies labelled with horseradish peroxidase (anti-IgG Px conjugate) r.t.u. CONJ 1 vial
- 55 mL Wash buffer, 10x concentrated WASH 10x 1 vial
- 60 mL Dilution buffer, r.t.u. DIL 1 vial
- 13 mL Chromogenic substrate TMB, r.t.u. (TMB/H2O2) TMB 1 vial
- 13 mL Urea solution, r.t.u. UREA 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
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试剂未包括
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- 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
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应用备注
- Optimal working dilution should be determined by the investigator.
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板类型
- Pre-coated
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实验流程
- anti-TBEV IgG and IgG avidity is a solid-phase immunoanalytical test. The polystyrene strips are coated with specific antigen which bear immunodominant epitopes of TBEV. Anti-TBEV antibodies in samples bind to the immobilized antigens. The antibodies that do not bind are washed away and those that formed complexes with the antigens are later on recognised by animal anti-human IgG antibodies labelled with horseradish peroxidase. The presence of labelled antibodies is revealed by an enzymatic reaction with a chromogenic substrate. Negative samples do not react and the mild change in colour, if present, may be attributed to the reaction background. To determine avidity, each sample is applied in parallel to two wells, with the appropriate antibodies binding to the immobilized antigens. In the next step, one well is incubated with the wash solution, the other well with the urea solution. In the first well, specific antibodies with high and low avidity remain bound to the antigen. In the second well, low-avidity antibodies are released due to the concentrated urea solution, and only high-avidity antibodies remain complex with the antigen. The ratio between the optical density of the well with the urea solution and the well with the washing solution in percent expresses the relative avidity index (RAI).
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限制
- 仅限研究用
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储存条件
- 4 °C
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- Tick-Borne Encephalitis Virus IgG and IgG Avidity
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物质类
- Antibody
抗原
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