FDP Coagulation Test
Description
The FDP Coagulation Test is specifically designed to check for any abnormalities in blood coagulation. By measuring the level of FDP in the bloodstream, this specialized test can effectively determine if there is a blood coagulation disorder present. Through immunoturbidimetry, the quantitative analysis of degraded fibrin/fibrinogen products in human plasma is carried out. The test employs a suspension of uniform-sized polystyrene latex particles. It efficiently measures fibrinogen degradation products (FDP) in the serum, making it a convenient and rapid latex agglutination test for diagnosing conditions such as disseminated intravascular coagulation (DIC), deep vein thrombosis (DVT), pulmonary embolism (PE), certain pregnancy-related disorders, and myocardial infarction.
Specimen Requirements:
Product name: FDP Coagulation Test
Type of Specimen: Plasma
Volume: 5μL
Container:Blue-top (sodium citrate) tube
The recommended assay entails using freshly collected plasma obtained from a sodium citrated whole blood sample, which is composed of nine parts venous blood mixed with one part 0.109M trisodium citrate. After the sample has been drawn, it should be centrifuged at 3000 rpm for a duration of 15 minutes, and the plasma ought to be immediately removed.
Test Procedure :
Sample/Control | 5μL | ||
Incubate for 20 seconds at 37℃ | |||
R1 | 100 μL | ||
Incubate for 90 seconds at 37℃ | |||
R2 | 100 μL | ||
After mixing thoroughly, measure the absorbance and compare it with the standard to obtain the desired results. It is crucial to ensure that the obtained content is similar to the original text content. However, to do so, it is essential to rearrange the text without altering its meaning. | |||
Parameters for testing can be adjusted in equal proportions, whether they need to be decreased or increased. This flexibility in adjusting the parameters allows for greater control and precision in the testing process. It ensures that any changes made to the parameters have the same effect on the overall testing procedure. By maintaining equal proportionality, the integrity and consistency of the tests are preserved. This approach allows for efficient optimization of the testing conditions and better evaluation of the tested system's performance.
Storage and Stability:
Storage: 2~8 ℃, do not freeze.
Closed Vial Expiry: 12 months.
After opening, R1 and R2 can only be stored for 30 days in a refrigerated environment of 2-8 ℃. Similarly, once dissolved, Level 1 and Level 2 will remain stable for a maximum of 7 days under the same conditions. It is important to adhere to these guidelines to ensure the effectiveness and reliability of the products.
Plasma Storage:
10℃~30℃ : 4 hours
2℃~8℃ : 24 hours
≤-18℃ ： 4 weeks
Specification:
Cat. No. | Compent | |||
R1 | R2 | R3 | R4 | |
1 | 4mLx 2 | 4mLx 2 | / | / |
2 | 4mLx 2 | 4mLx 2 | 1mL x 1 | 1mL x 1 |
3 | 4mLx 2 | 4mLx 2 | 1mL x 10 | 1mL x 10 |
4 | 6mLx4 | 6mLx4 | / | / |
5 | 6mLx4 | 6mLx4 | 1mL x 10 | 1mL x 10 |
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