answersLogoWhite

0

To prevent unspecific binding of antibody to the plastic of the microtiter plate.

User Avatar

Wiki User

16y ago

What else can I help you with?

Continue Learning about Natural Sciences

Describe the mechanism of Enzyme linked Immunosorbent Assay ELISA?

Enzyme Linked Immuno Sorbant Assay (ELISA) is so sensitive because of the detection method, i.e. using antibody, and visual detection. A positive control is needed because of the relative selectivity of the antibody. It can always bind to other stuff and give artifactually high values. Nonspecific, unoccupied binding sites in the microtiter plate (as well as other places) have to be blocked or they will give a signal as though they were the analyte of interest.


How do you say hi my name is elisa in spanish?

Hola me llamo Elisa. That is how you say hi my name is Elisa in Spanish.


What is Elisa used for?

Elisa (Enzyme-Linked Immunosorbent Assay) is a common laboratory technique used to detect the presence of antibodies or antigens in a sample. It is widely used in medical diagnostics, food testing, and research settings to identify and quantify specific molecules.


ELISA test what is a meaning of non reactive?

In the context of an ELISA test, "non-reactive" means that no antibodies or antigens of interest were detected in the sample. This result indicates the absence of a specific immune response to the tested substance.


When testing for HIV a test produces more accurate results than the ELISA test?

The Western blot test is often used as a confirmatory test after a positive ELISA result for HIV. It is more specific but can also produce false positive results due to its high sensitivity. Consulting a healthcare provider for interpretation of test results and appropriate follow-up is important in HIV testing.

Related Questions

What is the different between sandwich elisa and a competitive elisa?

There are different methods for different analytes.It is typically used sandwich ELISA for macromolecules.This name because two antibodies are combined with the analyte,the complexes like a sandwich. Competitive ELISA is suitable for small molecules that can't combine with two antibodies.In competitive ELISA,The antigen that be tested and the enzyme-labeled antigen compete for binding to the antibody that wascoatedThe antigen and the enzyme-labeled antigen compete for binding to the antibody that was coated on microtiter plates,so this method called competitive ELISA.Meretciel offer ELISA kits both sandwich ELISA and competitive ELISA.


What is indirect elisa?

In the Indirect ELISA ,An antigen is added to the microtiter plate well and the antigen attaches to the walls of the microtiter plate.After rinsing to remove excess antigen, the serum suspected of containing the antibodies is added.Enzyme-linked antibody capable of reacting with the constant region of other antibodies is the added, followed by addition of the colorless substrate. Development of color indicates the presence of the antibody being identified.


What is the effect of not including the antigen or the primary antibody in the ELISA reaction?

Not including the antigen will prevent the primary antibody from binding to it which will disrupt the results of the ELISA. Not including the primary antibody will prevent the secondary antibody from binding it, which will again negatively affect the results of the ELISA. All components are necessary to get an accurate ELISA.


Describe the mechanism of Enzyme linked Immunosorbent Assay ELISA?

Enzyme Linked Immuno Sorbant Assay (ELISA) is so sensitive because of the detection method, i.e. using antibody, and visual detection. A positive control is needed because of the relative selectivity of the antibody. It can always bind to other stuff and give artifactually high values. Nonspecific, unoccupied binding sites in the microtiter plate (as well as other places) have to be blocked or they will give a signal as though they were the analyte of interest.


How to store the detachable Elisa plate after disassembly?

The Hawach high binding Elisa plate is detachable. After disassembly, it can be put into a pollution-free bag and sealed, and stored in the refrigerator at 2-8 degrees.


What is the agid and elisa test?

The AGID test is the agar gel immunodiffusion test and ELISA is the enzyme-linked immunosorbent assay. Both test for the presence of certain proteins (called antigens) by binding them with antibodies.


What is elisa kits?

ELISA(enzyme-linked immunosorbent assay) is a method for detecting the concentration of some kind antigen or antibody,using the characteristic of specific binding between antigen-antibody. The method is suitable for determination of serum, plasma,tissue fluid, urine samples and cell culture supernatant.The ELISA kit is a useful tool to detect cytokines,hormones and Small molecules of food safety. Meretciel is one commmon brand of ELISA kits in China.


Why blocking buffer is used in Elisa?

Blocking buffer is used in ELISA to prevent non-specific binding of proteins or antibodies to the surface of the wells. By coating the surface with a blocking buffer, it helps to reduce background noise and increase the specificity of the assay by ensuring that the detection antibodies bind specifically to the target antigen.


When was Elisa's created?

Elisa's was created in 2009.


What is the birth name of Elisa Veek?

Elisa Veek's birth name is Elisa Vignochi Veeck.


What is the birth name of Elisa Aldridge?

Elisa Aldridge's birth name is Elisa Deanne Aldridge.


What is the birth name of Elisa Bridges?

Elisa Bridges's birth name is Elisa Rebeca Bridges.