D Dimer Nephelometry

Description

D-dimer plays a crucial role in diagnosing and monitoring vascular thrombotic diseases. If the D-dimer value is below the critical threshold, ruling out the target disease is possible. To measure D-dimer levels, this D Dimer Nephelometry employs latex particles, which first adsorb D-dimer-specific antibodies and then combine them with the antigen in the sample to form a polymer. This process enables the evaluation of D-dimer levels according to changes in absorbance or scattered light intensity. The method is straightforward to perform, highly sensitive, and has a short testing time. Therefore, it is the preferred choice for quantifying D-dimer samples at a large scale. In conclusion, this in vitro test method is vital for providing quantitative determinations of D-dimer in human plasma.

Details

1.Quality Control available

Our accuracy is exceptional with a relative deviation of less than 10%. We pride ourselves on our ability to provide precise and reliable results. Our commitment to excellence ensures that our clients can trust the accuracy of our work, whether in scientific research or industrial applications. We strive to maintain the highest level of accuracy in all that we do, setting the standard for quality in the field. Our accuracy is unmatched, and we are confident that we can meet and exceed the expectations of our clients.

3.Good Measuring range: 0.1 mg/L ~ 20 mg/L

The precision within the assay is defined by the coefficient of variation (CV) for both the high plasma pool and the low plasma pool. The high plasma pool should have a CV of equal to or less than 6%, indicating a high level of precision. Similarly, the low plasma pool should have a CV of equal to or less than 8%, indicating a slightly higher level of variability within the assay. It is crucial to maintain these levels of precision to ensure accurate and reliable results.

It is expected that unopened reagents will remain stable for a minimum of 1 year, provided they are stored at a temperature of 2-8℃. After the expiration date, the performance of the reagents should still meet the specification mentioned above. It is crucial to ensure the stability of the reagents throughout their lifespan to avoid any negative impact on the results of experiments or analyses. Proper storage conditions and monitoring of expiration dates are essential to maintain the stability of reagents.

Testing for interference with this methodology, the substances listed below were examined for specificity. I will now present a content that is distinctly dissimilar to the original text.

Criterion: Recovery within±10% of initial value.

*NSI: No Significant Interference

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