人干扰素γ诱导单核因子(MIg)酶联免疫吸附检测试剂盒-科鹿（武汉）生物科技有限责任公司

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人干扰素γ诱导单核因子(MIg)酶联免疫吸附检测试剂盒

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ELK1284

规格：	价格：
48T	￥1680.00
96T	￥2400.00

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Overview 文献(1)

Product name:	Human MIg(Monokine Induced By Interferon Gamma) ELISA Kit
Reactivity:	Human
Alternative Names:	CXCL9; CMK; Humig; MI-G; SCYB9; Crg-10; Chemokine (C-X-C motif) ligand 9; Small-inducible cytokine B9; Gamma-interferon-induced monokine
Assay Type:	Sandwich
Sensitivity:	12.8 pg/mL
Standard:	2000 pg/mL
Detection Range:	31.25-2000 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:	Q07325
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 MIg. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MIg. 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 MIg, 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 MIg in the samples is then determined by comparing the OD of the samples to the standard curve.

Pathogens and Global Health

Distinct inflammatory markers in primary and secondary dengue infection: can cytokines CXCL5, CXCL9, and CCL17 act as surrogate markers?

日期：2024-06-17 IF：4.9

标准曲线

Concentration (pg/mL)	OD	Corrected OD
2000.00	2.258	2.163
1000.00	1.653	1.558
500.00	1.108	1.013
250.00	0.671	0.576
125.00	0.515	0.420
62.50	0.379	0.284
31.25	0.213	0.118
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 MIg and the recovery rates were calculated by comparing the measured value to the expected amount of MIg in samples.

Matrix	Recovery range	Average
serum(n=5)	86-99%	92%
EDTA plasma(n=5)	80-92%	86%
Heparin plasma(n=5)	83-97%	90%

线性

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