Sichuan Vacure Prelab Biotechnology Co.,Ltd.

No.603,District 2,No.618,Kelin West Road
Chengdu Cross-Strait Science and Technology Industry Develop
Chengdu,  Sichuan  611100

China
http://vacurebiotech.com
  • Booth: 320


 Press Releases

  • This device is a quantitative determination analyzer developed basing on modern optoelectronic technology and intended to be used in combination with fluorescent immunoassay strips to detect relevant parameters of human samples. The detection results could be used for clinical auxiliary diagnosis.

    The analyzer applies a time-resolved method for detection. The principle is to use the characteristics of the wide Stocks shift and long duration of the lanthanide elements labeled in the test strip, that is, after removing the excitation light, the lanthanide elements can still maintain the continuous emission of the emitted light for a long time. However, other substances that can be excited to emit fluorescence cannot generate emission light in a very short time after the excitation light is removed. It is the application of the time-resolved method for detection that after turning off the excitation light for a certain period of time, and after other interfering substances cannot generate the emitted light, the light intensity is read. Through the optimized design of the optical path and the amplifier circuit, the weak fluorescence emission light signal can be detected, so as to achieve the purpose of reducing the background and interference.

  • This device is a quantitative determination analyzer developed basing on modern optoelectronic technology and intended to be used in combination with fluorescent immunoassay strips to detect relevant parameters of human samples. The detection results could be used for clinical auxiliary diagnosis.

    The analyzer applies a time-resolved method for detection. The principle is to use the characteristics of the long-lasting fluorescence of the lanthanide elements labeled in the test strip, that is, after removing the excitation light, the lanthanide elements can still maintain the continuous emission of the emitted light for a long time. However, other substances that can be excited to emit fluorescence cannot generate emission light in a very short time after the excitation light is removed. It is the application of the time-resolved method for detection that after turning off the excitation light for a certain period of time, and after other interfering substances cannot generate the emitted light, the light intensity is read. Through the optimized design of the optical path and the amplifier circuit, the weak fluorescence emission light signal can be detected, so as to achieve the purpose of reducing the background and interference.

  • The FIA HbA1c Test is intended for in vitro accuarate quantitative detection of HbA1c in whole blood and fingertip blood in 10 minutes with a CV of less than 5%.

     

    It is a blood test to diagnose type 2 diabetes. It is also used to monitor blood glucose control in people with diabetes.

    It is for professional use only.

  • (May 06, 2025)

    This Total Vitamin D FIA Test is based on the fluorescence immunoassay method for the quantitative detection of Vitamin D in multiple human samples by self-developed LYOFIA® system, including whole blood, serum and plasma sample.

    For in vitro diagnostic use only.

    A blood test for vitamin D can determine whether osteoporosis has occurred. Pathological elevations of vitamin D in the blood can be seen in tuberculosis, lymphoma, hypercalcemia, and kidney stones, and serum vitamin D levels in children are higher than in adults. If children are deficient in vitamin D, they may develop vitamin D deficiency rickets, which manifests as irritability, excessive sweating, bone deformities, and muscle laxity. If adults are deficient in vitamin D, it can mainly manifest as osteoporosis, muscle weakness, easy falls and fractures, etc. In severe cases, it can lead to osteomalacia.

  • (May 06, 2025)

    This hs-cTnI blood test is a rapid test to quantitatively detect the amount of hs-cTnI in mutiple blood samples from human.  It is detected by LYOFIA® platform from VACURE Biotech.

    It's for professional use only.
     

     

    Method: Microfluidic Fluorescent Immunoassay
    Test: LYOFIA® hs-cTnI
    Format: Cassette
    Time: 10mins
    Linearity: 9~50000pg/mL
    Reference Interval: ≤27 pg/mL

     

    Why VACURE

     

    • Accurate

        L.od to 9pg/mL

     

    • Fast

        The hs-cTnI blood test detects hs-cTnI amout  in 10minutes

     

    • Easy

        Simple work flow

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