人氧化三甲胺(TMAO)酶聯免疫吸附檢測試劑盒-武汉义森科技有限责任公司

産品中(zhōng)心

人氧化三甲胺(TMAO)酶聯免疫吸附檢測試劑盒

ELK8356

規格：	價格：
48T	￥1960.00
96T	￥2800.00

下(xià)載說明 ①

Overview 文獻

Product name:	Human TMAO(Trimethylamine-N-oxide) ELISA Kit
Reactivity:	Human
Alternative Names:	TMAO
Assay Type:	Sandwich
Sensitivity:	0.065 μmol/L
Standard:	10 μmol/L
Detection Range:	0.16-10 μmol/L
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 Human TMAO. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human 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 Human 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 Human TMAO in the samples is then determined by comparing the OD of the samples to the standard curve.

EXCLI Journal

Optimization of enzyme-linked immunosorbent assay kit protocol to detect trimethylamine N-oxide levels in humans

日期：2023-02-20 IF：4.6
Journal of Functional Foods

Effect of soluble dietary fiber on gut microbiota and derived metabolites in stage 3 to 5 chronic kidney disease patients: A randomized controlled trial

日期：2024-04-20 IF：5.6

标準曲線

Concentration (μmol/L)	OD	Corrected OD
10.00	2.256	2.168
5.00	1.628	1.540
2.50	1.216	1.128
1.25	0.752	0.664
0.63	0.509	0.421
0.32	0.265	0.177
0.16	0.196	0.108
0.00	0.088	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)	87-95%	91%
Heparin plasma(n=5)	81-95%	88%

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.