Double Antibody Latex Enhanced Retinol Binding Protein Detection Kit
A protein-binding and latex-enhanced technology, applied in biological testing, material inspection products, etc., can solve problems such as insufficient sensitivity and inability to simultaneously RBP, etc., to achieve the effect of ensuring accuracy
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Embodiment 1
[0060] Embodiment 1: RBP kit 1 composition
[0061] Reagent 1 component:
[0062] Buffer MOPS0.15mol / LpH=6.5,
[0063] PEG600010%,
[0064] NaN 3 0.1%,
[0065] EDTA100mmol / L,
[0066] Reagent 2 components:
[0067] Buffer MOPS0.15mol / LpH=8.5,
[0068] Monoclonal antibody A0.45mg / ml (source: mouse anti-human, antigen: retinol binding protein extracted from human urine, potency: greater than 1:5000),
[0069] Latex particle A (for monoclonal antibody A coating) 104nm 0.35% (manufacturer: JSR carboxyl content: 0.238meq / g, concentration: 5%),
[0070] Monoclonal antibody B0.5mg / ml (source: mouse anti-human, antigen: retinol binding protein extracted from human urine, potency: greater than 1:1000),
[0071] Latex particles B (for monoclonal antibody B coating) 77nm 0.5% (manufacturer: JSR, carboxyl content: 0.274meq / g, concentration: 5%),
[0072] Calibrators: Serum calibrators with concentrations of 130, 100, 50, 25, 12.5, 0mg / L,
[0073] Calibrator: urine calibrators, ...
Embodiment 2
[0074] Embodiment 2: The sensitivity performance evaluation of the kit 1 of the present application
[0075] Instrument: Olympus AU400
[0076] Table 1: Parameters:
[0077]
[0078] Urine calibrator 4, 2, 1, 0.5, 0.25, 0mg / L,
[0079] Control reagent:
[0080] A well-known foreign brand A:
[0081] Its main components:
[0082] Reagent R1: GOOD’S buffer,
[0083] Reagent R2: latex-coated rabbit anti-human RBP antibody IgG,
[0084] Detection principle:
[0085] Latex particles coated with multiple anti-RBP antibodies bind to the RBP antigen in the sample to form an immune complex, and the turbidity change is detected at 570nm, and the degree of change is proportional to the RBP content in the sample.
[0086] Urine calibrator 5, 2.5, 1.25, 0.625, 0.31, 0mg / L,
[0087] Sensitivity evaluation method:
[0088] Dilute the sample prepared from pure RBP so that a certain concentration is close to the sensitivity limit, repeat 10 times to detect the water blank and sampl...
Embodiment 3
[0108] Example 3: Linear performance evaluation of kit 1 of the present application
[0109] Instrument: Olympus 400
[0110] Table 8: Parameters:
[0111]
[0112] Serum calibrator: the concentrations are 130, 100, 50, 25, 12.5, 0mg / L,
[0113] Linear evaluation method:
[0114] Serum samples were diluted in a gradient of 1 / 10, 1 / 40, 1 / 20, 1 / 10, 2 / 10, 3 / 10, 4 / 10, 5 / 10, 6 / 10, 7 / 10, 8 / 10, 9 / 10, 1, each concentration was tested 3 times. Take the dilution ratio as the X-axis, and use the measured value as the Y-axis to draw a graph. The results are shown in figure 1 .
[0115] Table 9: Linearity detection data:
[0116]
[0117]Linear regression plotting was performed on the data, and the results are shown in the appendix figure 1 Evaluation criteria: The deviation between the detection and theoretical value should be within ±10%, which is acceptable.
[0118] Conclusion: when the sample concentration is greater than 130 mg / L, prozone will appear in the detection; t...
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