ELISA
 
Introduction to Elisa: Enzyme-Linked ImmunoSorbent Assay, or ELISA, is a biochemical technique used mainly in immunology to detect the presence of an antibody or an antigen in a sample. The ELISA has been used as a diagnostic tool in medicine and plant pathology, as well as a quality control check in various industries. In simple terms, in ELISA an unknown amount of antigen is affixed to a surface, and then a specific antibody is washed over the surface so that it can bind the antigen. This antibody is linked to an enzyme, and in the final step a substance is added that the enzyme can convert to some detectable signal. Thus in the case of fluorescence ELISA, when light is shone upon the sample, any antigen/antibody complexes will fluoresce so that the amount of antigen in the sample can be measured.

 

 

Protocol 1. Basic Elisa Protocol 

 

Protocol 2. Indirect Elisa Protocol

 

Protocol 2. Detection of recombinant proteins by Elisa

 

Protocol 3. The procedure for optimized Elisa Protocol

 

Protocol 4. Enzyme-Linked Immunosorbent Assay (ELISA) Protocol

 

Protocol 5. Double antibody sandwich Elisa (DAS-Elisa)

 

Protocol 6. Cytokine Elisa Protocol

 

Protocol 7. Qualitative PCR?CELISA protocol for the detection and typing of viral genomes

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Protocols / Immunology-immunohistology

Preparing silanized (+plus) slides

Microscopy Techniques
Electron microscopy
HE staining 
Nucleic acid stain
Special cell & cell fraction stains
Antibody purification
Antibody storage and handling
Conjugation of monoclonal antibodies 
Antigen retrieval
Elisa
FRQs for histochemistry
Immunoperoxidase staining techniques
Immunofluorohistochemistry  
Confocal microscope technique 
Laser Capture Microdissection
Immunoprecipitation
ChIP assay

Hybridization in situ

Histotechnology--technical methods

Flow cytometry (FCM)

Kinase assay
 

 

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