,,

產(chǎn)品中心

人轉(zhuǎn)化生長(zhǎng)因子β2(TGFb2)微量上樣酶聯(lián)免疫吸附檢測(cè)試劑盒

一鍵復(fù)制產(chǎn)品信息

ELK4829MS

規(guī)格：	價(jià)格：
48T	￥1960.00
96T	￥2800.00
96T*5	￥11900.00

下載說明 ①

Overview

Product name:	Human TGFb2(Transforming Growth Factor Beta 2) Microsample ELISA Kit
Reactivity:	Human
Alternative Names:	TGF-B2; TGF-Beta2; G-TSF;? LAP; Cetermin; Polyergin; Latency-associated peptide; BSC-1 cell growth inhibitor; Glioblastoma-derived T-cell suppressor factor
Assay Type:	Sandwich
Sensitivity:	9 pg/mL
Standard:	2000 pg/mL
Detection Range:	31.25-2000 pg/mL
Sample Type:	Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Assay Length:	3.5h
Research Area:	Cytokine;Infection immunity;
Uniprot ID:	P61812
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 TGFb2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TGFb2. 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 TGFb2, 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 TGFb2 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
2000.00	2.213	2.118
1000.00	1.707	1.612
500.00	1.120	1.025
250.00	0.753	0.658
125.00	0.596	0.501
62.50	0.318	0.223
31.25	0.200	0.105
0.00	0.095	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 TGFb2 and the recovery rates were calculated by comparing the measured value to the expected amount of TGFb2 in samples.

Matrix	Recovery range	Average
serum(n=5)	86-119%	103%
EDTA plasma(n=5)	90-120%	105%
Heparin plasma(n=5)	88-113%	101%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of TGFb2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.