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FAQs

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Q:

Are the plates pre-coated? How do I store the remaining wells or plates if I can't use them all at once?

A:

Yes. We provide pre-coated plates. The strips are detachable and it’s recommended to separate those wells needed for assay and store the rest at -20℃ without germ contamination.


Q:

What is the shelf life of OUR ELISA products?

A:

6 months since the production date. Please refer to the box label for the shelf life.


Q:

How to store the ELISA Kit?

A:

If the unopened kit is not supposed to be used up within 1 month, please store the Pre-coated Assay Plate, Standard, Biotin-antibody (100×), and Streptavidin-HRP (100×) at -20℃, other reagents at 2-8°C. , avoiding repeated freezing and thawing.

Opened reagents should be used as soon as possible. Unused parts should be stored properly and the date of opening should be recorded.


Q:

How long can I store lyophilized standards after dilution?

A:

It needs to be used within 24 hours.


Q:

Q: Can I use antibodies or reagents from different manufacturers?

A:

It is usually not recommended to use reagents from different manufacturers as they may be incompatible with other reagents in the Kit and may lead to inaccurate results.


Q:

How can I ensure reliable results from ELISA experiments?

A:

1) Ensure the linear range of the standard curve; 2) follow instructions closely and maintain reagent consistency; 3) perform duplicate experiments to increase the reliability of results.


Q:

How are ELISA results expressed?

A:

Typically, ELISA results can be expressed as optical density (OD) values, which are calculated and converted to the concentration of the target molecule (e.g. ng/mL or pg/mL).


Q:

What should I do if the results are abnormal?

A:

1)Check the reagent and sample preparation steps to ensure that there is no mishandling; 2) ensure that the reagents have not expired and check that the storage conditions are as required; 3) consider repeating the experiment if the results deviate significantly.


Q:

What is a common misconception in ELISA experiments?

A:

1)Not mixing samples or reagents sufficiently; 2) ignoring the effect of temperature and time on the experimental results; 3) inappropriate choice of standard curve range.


Q:

What is the reason for the low or high signal intensity?

A:

Low signal: This may be related to low sample concentration, insufficient reaction time, or reagent inactivation.

High signal: This may be due to high sample concentration, improper operation, etc.


Q:

How to deal with ELISA waste?

A:

Waste generated from ELISA experiments (e.g., samples, reagent tubes, etc.) should be disposed of under biosafety regulations to ensure that they do not pose a hazard to the environment or health.


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