人骨橋素(OPN)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

人骨橋素(OPN)酶聯免疫吸附檢測試劑盒

ELK1047

規格：	價格：
48T	￥1680.00
96T	￥2400.00

下(xià)載說明 ①

Overview 文獻

Product name:	Human OPN(Osteopontin) ELISA Kit
Reactivity:	Human
Alternative Names:	SPP1; BNSP; BSPI; ETA1; Secreted Phosphoprotein 1; Bone Sialoprotein I; Early T-Lymphocyte Activation 1; Nephropontin; Urinary stone protein; Uropontin
Assay Type:	Sandwich
Sensitivity:	0.263 ng/mL
Standard:	40 ng/mL
Detection Range:	0.63-40 ng/mL
Sample Type:	serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length:	3.5h
Research Area:	Tumor immunity;Bone metabolism;
Uniprot ID:	P10451
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 OPN. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human OPN. 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 OPN, 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 OPN in the samples is then determined by comparing the OD of the samples to the standard curve.

CLINICS

Patients who received sleeve gastrectomy have lower plasma osteopontin levels than those who did not

日期：2024-04-01 IF：2.7

标準曲線

Concentration (ng/mL)	OD	Corrected OD
40.00	2.095	1.940
20.00	1.621	1.466
10.00	1.088	0.933
5.00	0.677	0.522
2.50	0.441	0.286
1.25	0.289	0.134
0.63	0.239	0.084
0.00	0.155	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 OPN and the recovery rates were calculated by comparing the measured value to the expected amount of OPN in samples.

Matrix	Recovery range	Average
serum(n=5)	80-95%	87%
EDTA plasma(n=5)	90-107%	98%
Heparin plasma(n=5)	87-99%	93%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of OPN and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.