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人凝血因子ⅩⅢ(F13)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK1767

規(guī)格：	價(jià)格：
48T	￥1960.00
96T	￥2800.00

下載說(shuō)明 ①

Overview

Product name:	Human F13(Coagulation Factor XIII) ELISA Kit
Reactivity:	Human
Alternative Names:	FXIII; Fibrin Stabilizing Factor
Assay Type:	Sandwich
Sensitivity:	8 pg/mL
Standard:	1600 pg/mL
Detection Range:	25-1600 pg/mL
Sample Type:	plasma
Assay Length:	3.5h
Research Area:	Metabolic pathway;Hematology;
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 F13. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human F13. 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 F13, 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 F13 in the samples is then determined by comparing the OD of the samples to the standard curve.

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
1600.00	2.126	2.041
800.00	1.651	1.566
400.00	1.106	1.021
200.00	0.835	0.750
100.00	0.539	0.454
50.00	0.397	0.312
25.00	0.288	0.203
0.00	0.085	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 F13 and the recovery rates were calculated by comparing the measured value to the expected amount of F13 in samples.

Matrix	Recovery range	Average
serum(n=5)	96-107%	101%
EDTA plasma(n=5)	90-105%	97%
Heparin plasma(n=5)	85-97%	91%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of F13 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.