Kit for specifically detecting peptidoglycan
A technology of peptidoglycan and kits, which is applied in the field of kits for specific detection of peptidoglycans. It can solve the problems of inability to interpret chromogenic results, low sensitivity, mixed detection, etc., and meet the needs of clinical detection, sensitivity and The effect of high specificity and high coincidence rate
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Embodiment 1
[0019] A. Preparation of detection kits
[0020] Treatment solution: 0.5% KOH; biological buffer solution: 1% TAPS; diluent: pyrogen-free water; prophenoloxidase: obtained by extracting silkworm hemolymph and freeze-drying; chromogenic agent A: 5% 3,4-di Hydroxyphenylacetic acid (DhyAcA); Chromogenic agent B: 3% dopa; Standard: 1% peptidoglycan pyrogen-free aqueous solution, 3% peptidoglycan pyrogen-free aqueous solution, 5% peptidoglycan pyrogen-free aqueous solution, 7% Peptidoglycan pyrogen-free aqueous solution, 9% peptidoglycan pyrogen-free aqueous solution; stop solution: 8% citric acid.
[0021] B, the using method of kit of the present invention is:
[0022] 1) Sample pretreatment: Aseptic operation, extract 4ml of venous blood with a special non-pyrogenic vacuum blood collection tube (heparin anticoagulant), shake gently, and centrifuge at a speed of 3000rpm for 1 minute to obtain platelet-rich plasma; 40ul of plasma was added to the microplate, and 70ul of the trea...
Embodiment 2
[0027] A. Preparation of detection kits:
[0028] Treatment solution: 1% NaOH; biological buffer solution: 2% EPPS; diluent: pyrogen-free water; preparation of prophenoloxidase: extract the hemolymph of Mellonella mellonella moth and freeze-dry it; Color agent B: 3% catechol; standard product: 2% peptidoglycan pyrogen-free aqueous solution, 4% peptidoglycan pyrogen-free aqueous solution, 6% peptidoglycan pyrogen-free aqueous solution, 8% peptidoglycan pyrogen-free aqueous solution , 10% peptidoglycan pyrogen-free aqueous solution; stop solution: 5% benzoic acid.
[0029] B, the using method of kit of the present invention is:
[0030]1) Sample pretreatment: Aseptic operation, extract 4ml of venous blood with a special non-pyrogenic vacuum blood collection tube (heparin anticoagulant), shake gently, and centrifuge at a speed of 3000rpm for 1 minute to obtain platelet-rich plasma; 50ul of plasma was added to the microplate, and 80ul of the treatment solution was added. After s...
Embodiment 3
[0035] A. Preparation of detection kits
[0036] Treatment solution: 2% KOH; diluent: pyrogen-free water; prophenoloxidase: extracted from silkworm hemolymph and freeze-dried; color reagent A: 6% 3,4-dihydroxyphenylacetic acid (DhyAcA); Color agent B: 3.7% dopa; Standard product: 1% peptidoglycan pyrogen-free aqueous solution, 3% peptidoglycan pyrogen-free aqueous solution, 5% peptidoglycan pyrogen-free aqueous solution, 7% peptidoglycan pyrogen-free aqueous solution, 9% peptidoglycan pyrogen-free aqueous solution; stop solution: 7% citric acid.
[0037] B, the using method of kit of the present invention is:
[0038] 1) Sample pretreatment: Aseptic operation, extract 4ml of venous blood with a special non-pyrogenic vacuum blood collection tube (heparin anticoagulant), shake gently, and centrifuge at a speed of 3000rpm for 1 minute to obtain platelet-rich plasma; 40ul of plasma was added to the microplate, and 80ul of the treatment solution was added. After shaking well, the...
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