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人TGFβ誘導(dǎo)早期應(yīng)答基因1(TIEG1)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK1827

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

下載說(shuō)明 ①

Overview

Product name:	Human TIEG1(TGF Beta Inducible Early Response Gene 1) ELISA Kit
Reactivity:	Human
Alternative Names:	KLF10; EGRA; TIEG; Krueppel-Like Factor 10; TGFB Inducible Early Growth Response; EGR-alpha; Transforming growth factor-beta-inducible early growth response protein 1
Assay Type:	Sandwich
Sensitivity:	0.119 ng/mL
Standard:	20 ng/mL
Detection Range:	0.32-20 ng/mL
Sample Type:	Tissue homogenates, cell lysates and other biological fluids.
Assay Length:	3.5h
Research Area:	Signal transduction;Apoptosis;Tumor immunity;Infection immunity;Hepatology;
Uniprot ID:	Q13118
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 TIEG1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TIEG1. 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 TIEG1, 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 TIEG1 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
20.00	2.268	2.183
10.00	1.647	1.562
5.00	0.935	0.850
2.50	0.752	0.667
1.25	0.543	0.458
0.63	0.335	0.250
0.32	0.179	0.094
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 TIEG1 and the recovery rates were calculated by comparing the measured value to the expected amount of TIEG1 in samples.

Matrix	Recovery range	Average
serum(n=5)	82-95%	88%
EDTA plasma(n=5)	90-105%	97%
Heparin plasma(n=5)	87-99%	93%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of TIEG1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.