Elisa Teaching KIts

Product Price :Get Latest Price

Product Details:

The Sandwich ELISA measures the amount of antigen between two layers of antibodies (i.e. capture and detection antibody). The antigen to be measured must contain at least two antigenic sites capable of binding to antibody, since at least two antibodies act in the sandwich.Either monoclonal or polyclonal antibodies can be used as the capture and detection antibodies in Sandwich ELISA systems. Monoclonal antibodies recognize a single epitope that allows fine detection and quantification of small differences in antigen. A polyclonal is often used as the capture antibody to pull down as much of the antigen as possible.

Components

• Antigen (-20°C)
• Antibody (4°C)
• Coating buffer (4°C)
• Blocker (4°C)
• 96 well plate (RT)
• 1X PBST (RT)
• 10X Wash Buffer (RT)
• Antibody-HRP Conjugate (4°C)
• Stop solution (4°C)
• DAB(Chromogen) (4°C)
• H2O2(Substrate) (4°C)
• Protocol

Product Price :Get Latest Price

Product Details:

Antibody capture ELISA is a sophisticated, complex test that has proved useful in the diagnosis of many infectious diseases (e.g. rubella, measles, and toxoplasmosis). Antibody capture ELISA are particularly sensitive in demonstrating IgM responses early in illness. Reasons for this increase in sensitivity are: specific antibody isotypes in the patient''s specimen are bound to the solid phase by the capture antibody allowing the specific antibody-antigen reaction to occur in the absence of competing isotypes; soluble antigen is added in excess (allowing the antigen and antibody to react in antigen excess); and the antibody capture ELISA measures the proportion of specific to total antibody of a given isotype (which may be detectable earlier than simply measuring specific antibodies as in an ELISA test).

Components

• Antigen (-20°C)
• Blocking buffer (4°C)
• Test Antibody (-20°C)
• Antibody (Stock) (-20°C)
• Secondary Antibody( HRP- Conjugate) (-20°C)
• Coating Buffer (4°C)
• 10X PBS (RT)
• 96 well plate (RT)
• Stop solution (RT)
• Substrate (4°C)
• Wash buffer (RT)
• Protocol

Product Price :Get Latest Price

Product Details:

In this technique, antibody is first incubated in solution with a sample containing antigen. The antigen-antibody mixture is then added to an antigen coated microtiter well. The more antigen present in the sample, the less free antibody will be available to bind to the antigen-coated well. Addition of an enzyme-conjugated secondary antibody (Ab2) specific for the isotype of the primary antibody can be used to determine the amount of primary antibody bound to the well as in an indirect ELISA. In the competitive assay, however, the higher the concentration of antigen in the original sample, the lower the absorbance.

Components

• Antibody (-20 DegreeC)
• Antigen (1mg/ml stock) (-20 DegreeC)
• Blocking buffer (4 DegreeC)
• Coating Buffer (4 DegreeC)
• Secondary Antibody( HRP- Conjugate) (-20 DegreeC)
• Test Antigen (-20 DegreeC)
• 10X PBS (RT)
• 96 well plate (RT)
• Stop solution (RT)
• Substrate (4 DegreeC)
• Wash buffer (RT)
• Protocol

MOQ 5 Exps