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氧化三甲胺(TMAO)酶聯(lián)免疫吸附檢測(cè)試劑盒
ELK8678
規(guī)格: 價(jià)格:
48T ¥1960.00
96T ¥2800.00

Overview 文獻(xiàn)

Product name: TMAO(Trimethylamine-N-oxide) ELISA Kit
Reactivity: General
Alternative Names: TMAO
Assay Type: Sandwich
Sensitivity: 4.93 ng/mL
Standard: 1000 ng/mL
Detection Range: 15.63-1000 ng/mL
Sample Type: serum, plasma, cell lysates, cell culture supernates and other biological fluids
Assay Length: 3.5h
Research Area: Immunology;Innate Immunity;Complement;Alternative Pathway, Immunology;Innate Immunity;Complement;Other
Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to TMAO. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TMAO. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain TMAO, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of TMAO in the samples is then determined by comparing the OD of the samples to the standard curve.

標(biāo)準(zhǔn)曲線

Concentration (ng/mL) OD Corrected OD
1000.00 1.952 1.855
500.00 1.582 1.485
250.00 1.116 1.019
125.00 0.896 0.799
62.50 0.555 0.458
31.25 0.364 0.267
15.63 0.225 0.128
0.00 0.097 0.000

精密度

Intra-assay Precision (Precision within an assay):CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays):CV%<10%

Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.

回收率

Matrices listed below were spiked with certain level of recombinant TMAO and the recovery rates were calculated by comparing the measured value to the expected amount of TMAO in samples.
Matrix Recovery range Average
serum(n=5) 83-97% 90%
EDTA plasma(n=5) 78-92% 85%
Heparin plasma(n=5) 80-95% 87%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of TMAO and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Matrix 1:2 1:4 1:8 1:16
serum(n=5) 85-94% 87-96% 89-101% 82-90%
EDTA plasma(n=5) 83-96% 81-94% 86-98% 92-101%
Heparin plasma(n=5) 83-96% 86-95% 90-102% 81-93%
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