人促血管生(shēng)成素1(ANG1)酶聯免疫吸附檢測試劑盒-武汉义森科技有限责任公司

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人促血管生(shēng)成素1(ANG1)酶聯免疫吸附檢測試劑盒

ELK1005

規格：	價格：
48T	￥1680.00
96T	￥2400.00

下(xià)載說明 ①

Overview

Product name:	Human ANG1(Angiopoietin1) ELISA Kit
Reactivity:	Human
Alternative Names:	ANG1; AGP1; AGPT; ANG-I; ANGPT1; Angiopoietin 1
Assay Type:	Sandwich
Sensitivity:	0.11 ng/mL
Standard:	15 ng/mL
Detection Range:	0.24-15 ng/mL
Sample Type:	Serum, plasma, tissue homogenates and other biological fluids
Assay Length:	3.5h
Research Area:	Tumor immunity;Cardiovascular biology;
Uniprot ID:	Q15389
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 ANG1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ANG1. 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 ANG1, 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 ANG1 in the samples is then determined by comparing the OD of the samples to the standard curve.

标準曲線

Concentration (ng/mL)	OD	Corrected OD
15.00	2.035	1.932
7.50	1.593	1.490
3.75	1.194	1.091
1.88	0.831	0.728
0.94	0.582	0.479
0.47	0.363	0.260
0.24	0.215	0.112
0.00	0.103	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 ANG1 and the recovery rates were calculated by comparing the measured value to the expected amount of ANG1 in samples.

Matrix	Recovery range	Average
serum(n=5)	82-94%	88%
EDTA plasma(n=5)	85-97%	91%
Heparin plasma(n=5)	81-93%	87%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of ANG1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.