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人白介素17F(IL17F)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK1779

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

下載說(shuō)明 ①

Overview

Product name:	Human IL17F(Interleukin 17F) ELISA Kit
Reactivity:	Human
Alternative Names:	IL-17F; ML-1
Assay Type:	Sandwich
Sensitivity:	2.7 pg/mL
Standard:	500 pg/mL
Detection Range:	7.82-500 pg/mL
Sample Type:	serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length:	3.5h
Research Area:	Cytokine;Tumor immunity;Infection immunity;Immune molecule;
Uniprot ID:	Q96PD4
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 IL17F. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IL17F. 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 IL17F, 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 IL17F 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
500.00	1.948	1.861
250.00	1.593	1.506
125.00	1.183	1.096
62.50	0.852	0.765
31.25	0.553	0.466
15.63	0.331	0.244
7.82	0.190	0.103
0.00	0.087	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 IL17F and the recovery rates were calculated by comparing the measured value to the expected amount of IL17F in samples.

Matrix	Recovery range	Average
serum(n=5)	81-97%	89%
EDTA plasma(n=5)	84-99%	91%
Heparin plasma(n=5)	79-91%	85%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of IL17F and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.