Simplified fungus 1-3-beta-D glucan detection kit
A detection kit, dextran technology, which is applied in the direction of material analysis, biochemical instruments, and biochemical cleaning devices by observing the impact on chemical indicators, which can solve the problems of easy introduction of interfering substances, long detection time, and low accuracy. and other problems, to achieve the effect of shortening the operation time, reducing the procurement cost and facilitating the operation.
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Embodiment 1
[0026] Example 1: Preparation of detection kit
[0027] Such as figure 1 As shown, the kit includes a box body 10, an integrated reagent filling and reaction device 20, a main reaction agent 30, a main agent compound solution 40, a sample processing solution 50, and a quality control product 60:
[0028] Preparation of main reaction agent 30: Add factor B, factor C inhibitor—serine protease inhibitor, and peptide color matrix Boc-Leu-Gly-Arg—PNA-Cl or Boc-Ile-Gly-Arg— to the lysate of horseshoe crab blood cells PNA-Cl, so that the content of serine protease inhibitor in each milliliter of solution is 0.5-3mg, and the content of peptide color matrix is 0.5-2mg. Stir and mix the solution evenly and dispense it into the reaction cup, the volume is between 50-200ul , Vacuum freeze-drying is carried out to obtain the main reaction agent 30. The excipient is one or a combination of mannitol, lactose, glycine, and skim milk.
[0029] Preparation of main compound solution 40: Weigh Tris ...
Embodiment 2
[0033] Example 2 Use of integrated reagent filling and reaction device
[0034] Such as figure 2 As shown, a reagent filling and reaction device provided by the present invention includes a reaction cup 1, a rear chamber 2, a front chamber 3, and a push rod 4 connected in sequence, and the push rod 4 is inserted into the front chamber 3 and oriented relative to the front chamber 3. The inner movement pierces the sealing film 33 at the bottom of the front cabin 3, so that the push rod 4 and the front cabin 3 form an integral body. The rear cabin 2 moves inward to pierce the cone structure at the bottom of the rear cabin 2, the outer wall of the front cabin 3 and the inner wall of the rear cabin 2. In a sealed fit, the push rod 4, the front chamber 3, and the rear chamber 2 form an integrally moving inner cavity of the reaction cup 1, and the outer wall of the rear chamber 2 and the inner wall of the reaction cup 1 are in a sealed fit.
[0035] The outer sides of the upper end of th...
Embodiment 3
[0044] Example 3 Detection steps
[0045] Specific use:
[0046] 1) Sample processing: Aseptically, draw 4ml of venous blood with a dedicated pyrogen-free vacuum serum collection tube, shake it gently, leave it at room temperature for about 30 minutes, and then centrifuge it in a low-temperature centrifuge at 1000 rpm for 10-15 minutes, use a pipette or 15-80ul of serum is sucked by a Pasteur pipette and added to the front chamber 3 containing the sample processing solution 50, placed in the automatic microplate reader (model), shaken and mixed, and incubated for 5-15 minutes.
[0047] 2) After the incubation is completed, the automatic microplate reader will automatically press the integrated reagent filling and reaction pack 20, so that the push rod 4 pierces the sealing film at the lower end of the front chamber 3, and the sample processing solution 50 in the front chamber 3 flows with the sample together Rear chamber 2, mix with the main agent compound solution 40 in rear chambe...
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