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人10kDa干擾素γ誘導(dǎo)蛋白(IP10)酶聯(lián)免疫吸附檢測試劑盒

ELK1278

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

下載說明 ①

Overview 文獻(xiàn)

Product name:	Human IP10(Interferon Gamma Induced Protein 10kDa) ELISA Kit
Reactivity:	Human
Alternative Names:	CXCL10; C7; IFI10; INP10; SCYB10; Crg2; GIP10; Mob1; Chemokine C-X-C Motif Ligand 10; Small Inducible Cytokine Subfamily B(Cys-X-Cys)Member 10
Assay Type:	Sandwich
Sensitivity:	6 pg/mL
Standard:	1000 pg/mL
Detection Range:	15.63-1000 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;
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 IP10. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IP10. 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 IP10, 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 IP10 in the samples is then determined by comparing the OD of the samples to the standard curve.

WOUND REPAIR AND REGENERATION

Foamy macrophages potentially inhibit tuberculous wound healing by inhibiting the TLRs/NF-κB signalling pathway

日期：2022-04-06 IF：3.617

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
1000.00	2.035	1.940
500.00	1.717	1.622
250.00	1.194	1.099
125.00	0.831	0.736
62.50	0.582	0.487
31.25	0.363	0.268
15.63	0.258	0.163
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 IP10 and the recovery rates were calculated by comparing the measured value to the expected amount of IP10 in samples.

Matrix	Recovery range	Average
serum(n=5)	92-105%	98%
EDTA plasma(n=5)	90-105%	97%
Heparin plasma(n=5)	85-97%	91%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of IP10 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.