CE Certification Troponin I Result Suppliers – Troponin I test – Laihe

CE Certification Troponin I Result Suppliers – Troponin I test – Laihe


Sample type:

    Product Advantage:

    • High Detection accuracy
    • High cost performance
    • Quality assurance
    • Fast delivery
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    CE Certification Troponin I Result Suppliers –Troponin I test – LaiheDetail:

    WechatIMG1795

    Please read the instructions carefully before use and the dry fluorescence immunoanalyzer of Hangzhou Laihe Biotech Co.,Ltd.

    (1)Preparation: open the dry fluorescence immunoanalyzer of Hangzhou Laihe Biotech Co.,Ltd.

    (2)Prior to testing reagent, buffer, reaction tube sealed refrigeration, ID card and sample return to room temperature under test (15-30℃),the recommended reagents is restored to room temperature and opended.

    (3)Calibration: Confirm that the ID card is matched with the batch number of the reagent, insert ID card after correct, and click read ID card after entering the test interface, and the reagent can be detected after the calibration is completed.

    (4)Add the sample:

    ①75μl mixture into the reagent plate.

    ②Tube detection buffer injection method:If the samples were to be tested, the serum/plasma would be removed 75μl, if the whole blood sample is removed from 150μl to the detection buffer,fully mix (30s-1min), and absorb 75μl mixture into the reagent plate.

    (5)Modle:
    According to the type of sample, the serum/plasma mode or whole blood mode is selected in the sample type option on the dry fluorescence immunoanalyzer.

    (6)Test:
    ①Standard test: when the reagent card is added, the device will be inserted immediately, then click the “test button” the system will automatically countdown, and the automatic reading card will give the test results.

    ②Instant test: After the reagent card is added, the external reaction of the machine is 12 minutes, after the reaction, the reagent card is inserted into the instrument. Click the “test button”, the system will automatically read the card and give the test results.

    (7)Click “print” and the system will automatically print the test results on the printer paper.

    (8)After test of the reagent card, the excess premix, the used tip and the excess clinical sample were inactivated.


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