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A d-dimer latex-enhanced immune turbidimetric detection kit used in conjunction with an ion stabilizer and a suspension stabilizer

A suspension stabilizer and detection kit technology, which is applied in the field of D-dimer latex-enhanced immunoturbidimetric detection kits, can solve time-consuming problems, achieve the effects of increasing sensitivity, ensuring cross-linking effect, and simplifying operation methods

Active Publication Date: 2016-03-30
ZYBIO INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, colloidal gold method is widely used clinically. ELISA operation is strict and time-consuming. As a qualitative or semi-quantitative method, colloidal gold is slightly insufficient for quantification.

Method used

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  • A d-dimer latex-enhanced immune turbidimetric detection kit used in conjunction with an ion stabilizer and a suspension stabilizer
  • A d-dimer latex-enhanced immune turbidimetric detection kit used in conjunction with an ion stabilizer and a suspension stabilizer
  • A d-dimer latex-enhanced immune turbidimetric detection kit used in conjunction with an ion stabilizer and a suspension stabilizer

Examples

Experimental program
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Effect test

Embodiment 1

[0039] A D dimer latex enhanced immune turbidimetric detection kit, comprising the following preparation steps:

[0040] (1) Preparation of reagent R1:

[0041] Weigh 1.9g stachyose, 0.5g alum, 1.9g sodium fructose diphosphate, 0.3g sodium hexametaphosphate, 1.8g glycine, 27gNaCl, 35gPEG8000, 0.5g sodium azide, 10g bovine serum albumin and 1.42g EDTA dissolved in Adjust the pH to 7.4 in 0.8L distilled water, and dissolve 1L to obtain reagent R1.

[0042] (2) Preparation of reagent R2:

[0043] The above-mentioned washed polystyrene latex microspheres were diluted to a mass concentration of 1% with PBS buffer solution having a pH of 7.4 and a concentration of 50 mmol / L. Add 0.01g of EDC to 1L of the above latex dilution, stir and react at room temperature for 60min, centrifuge after the reaction and wash with PBS buffer to remove unreacted EDC, then add D-dimer antibody, stir and react at 37°C for 4h , add stop solution for 4h to terminate the reaction, centrifuge and wash t...

Embodiment 2

[0045] A D dimer latex enhanced immune turbidimetric detection kit, comprising the following preparation steps:

[0046] (1) Preparation of reagent R1:

[0047] Weigh 1.9g of stachyose, 0.5g of alum, 1.9g of sodium fructose diphosphate, 0.3g of sodium hexametaphosphate, 1.8g of glycine, 30g of NaCl, 50g of PEG8000, 0.5g of sodium azide, 50g of bovine serum albumin and 7.1g of EDTA in Adjust the pH to 7.4 in 0.8L distilled water, and dissolve 1L to obtain reagent R1.

[0048] (2) Preparation of reagent R2:

[0049] Dilute the polystyrene latex microspheres to a mass concentration of 3% with MES buffer solution with a pH of 6.5 and a concentration of 100 mmol / L. Add 0.01g of EDC to 1L of the above latex dilution, stir and react at room temperature for 30min, centrifuge after the reaction and wash with PBS buffer to remove unreacted EDC, then add D-dimer antibody, stir and react at room temperature for 8h, Add stop solution for 4h to terminate the reaction, centrifuge and wash...

Embodiment 3

[0051] A D dimer latex enhanced immune turbidimetric detection kit, comprising the following preparation steps:

[0052] (1) Preparation of reagent R1:

[0053] Weigh 1.9g of stachyose, 0.5g of alum, 1.9g of sodium fructose diphosphate, 0.3g of sodium hexametaphosphate, 1.8g of glycine, 15g of NaCl, 24g of PEG8000, 0.5g of sodium azide, 10g of bovine serum albumin and 7.1g of EDTA in Adjust the pH to 7.4 in 0.8L distilled water, and dissolve 1L to obtain reagent R1.

[0054] (2) Preparation of reagent R2:

[0055] Dilute the polystyrene latex microspheres to a mass concentration of 2% with MES buffer at a pH of 6.0 and a concentration of 100 mmol / L. Add 0.02g of EDC to 1L of the above latex dilution, stir and react at room temperature for 30min, centrifuge after the reaction and wash with PBS buffer to remove unreacted EDC, then add D-dimer antibody, stir and react at room temperature for 8h, Add stop solution for 4h to terminate the reaction, centrifuge and wash the obtain...

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Abstract

The invention relates to an in vitro diagnostic kit and in particular relates to a D-dimmer latex-reinforced immunonephelometry detection kit cooperatively adopting an ion stabilizer and a suspension stabilizer. The D-dimmer latex-reinforced immunonephelometry detection kit cooperatively adopting the ion stabilizer and the suspension stabilizer comprises two components, namely a reagent R1 and a reagent R2, wherein the reagent R1 mainly consists of a buffer solution 1, a stabilizer 1, a preservative 1, a coagulation accelerator and a protective agent 1; the reagent R2 mainly consists of a buffer solution 2, two polystyrene latex microspheres crosslinked with different D-dimmer monoclonal antibodies, a stabilizer 2, a protective agent 2 and a preservative 2, and the stabilizer 2 in the reagent R2 adopts the ion stabilizer and the suspension stabilizer which are used cooperatively. Compared with the prior art, the D-dimmer latex-reinforced immunonephelometry detection kit cooperatively adopting the ion stabilizer and the suspension stabilizer has the advantages that a latex-reinforced immunonephelometry method is adopted, and detection can be carried out under the condition that wavelength is 400-800nm, so that the detection is easier and the D-dimmer latex-reinforced immunonephelometry detection kit cooperatively adopting the ion stabilizer and the suspension stabilizer can be applied in clinical more easily.

Description

technical field [0001] The invention relates to an in vitro diagnostic kit, in particular to a D-dimer latex-enhanced immune turbidimetric detection kit used in conjunction with an ion stabilizer and a suspension stabilizer. Background technique [0002] The fibrinolytic system is the most important anticoagulant system in the human body and consists of four main components: plasminogen, plasminogen activator, plasmin, and plasmin inhibitor. When a fibrin clot is formed, in the presence of plasminogen activators, plasminogen is activated and converted into plasmin, the process of fibrinolysis begins, and plasmin degrades the fibrin clot to form various soluble fragments, Formation of fibrin product (FDP), FDP is composed of X-oligomer, D-dimer, middle fragment and fragment E (FragmentE). Among them, both X-oligomer and D-mer contain D-dimer unit. [0003] The fibrinolytic system of the human body plays an important role in maintaining the normal permeability of blood vesse...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/577
CPCG01N33/577
Inventor 高昂
Owner ZYBIO INC