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人干擾素α(IFNa)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK1043

規(guī)格：	價(jià)格：
48T	￥1680.00
96T	￥2400.00

下載說(shuō)明 ①

Overview 文獻(xiàn)

Product name:	Human IFNa(Interferon Alpha) ELISA Kit
Reactivity:	Human
Alternative Names:	IFNα1; IFL; LeIF D; IFN; IFN-Alpha; IFNα13; IFN-A; IFNαP22; IFN-Alpha 1b; Interferon Alpha 1b; Interferon, Leukocytic; IFN, Leukocyte; Interferon alpha-D
Assay Type:	Sandwich
Sensitivity:	3 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;Infection immunity;
Uniprot ID:	P01562
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 IFNa. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IFNa. 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 IFNa, 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 IFNa in the samples is then determined by comparing the OD of the samples to the standard curve.

AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY

Active Heme Metabolism Suppresses Macrophage Phagocytosis via the TLR4/Type I IFN Signaling/CD36 in Uterine Endometrial Cancer

日期：2024-08-21 IF：2.1

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
500.00	2.274	2.204
250.00	1.359	1.289
125.00	0.701	0.631
62.50	0.365	0.295
31.25	0.211	0.141
15.63	0.179	0.109
7.82	0.087	0.017
0.00	0.070	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 IFNa and the recovery rates were calculated by comparing the measured value to the expected amount of IFNa in samples.

Matrix	Recovery range	Average
serum(n=5)	83-92%	85%
EDTA plasma(n=5)	84-108%	98%
Heparin plasma(n=5)	87-96%	92%

線性

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