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斑馬魚(yú)白介素1β(IL1β)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK0988

規(guī)格：	價(jià)格：
48T	￥2240.00
96T	￥3200.00

下載說(shuō)明 ①

Overview 文獻(xiàn)

Product name:	Zebrafish IL1β(Interleukin 1 Beta) ELISA Kit
Reactivity:	Zebrafish
Alternative Names:	IL-1B;IL1-B; IL1-Beta; IL1F2; IL-1β; Interleukin-1 Family Member 2; Catabolin
Assay Type:	Sandwich
Sensitivity:	1.37 pg/mL
Standard:	200 pg/mL
Detection Range:	3.13-200 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;
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 Zebrafish IL1β. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Zebrafish IL1β. 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 Zebrafish IL1β, 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 Zebrafish IL1β in the samples is then determined by comparing the OD of the samples to the standard curve.

Clinical Complementary Medicine and Pharmacology

A Single Dose Intraperitoneal Injection of P. gingivalis Outer Membrane Vesicle (OMV) Stimulated Expressions of Neuroinflammatory Markers and Histopathological Changes in the Brain of Adult Zebrafish

日期：2024-09-10 IF：0

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
200.00	2.096	2.014
100.00	1.527	1.445
50.00	1.223	1.141
25.00	0.828	0.746
12.50	0.487	0.405
6.25	0.318	0.236
3.13	0.189	0.107
0.00	0.082	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 IL1β and the recovery rates were calculated by comparing the measured value to the expected amount of IL1β in samples.

Matrix	Recovery range	Average
serum(n=5)	82-95%	88%
EDTA plasma(n=5)	87-95%	91%
Heparin plasma(n=5)	80-97%	88%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of IL1β and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.