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小鼠消退素D1(RvD1)酶聯(lián)免疫吸附檢測(cè)試劑盒

一鍵復(fù)制產(chǎn)品信息

ELK0494

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

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Overview 文獻(xiàn)(2)

Product name:	Mouse RvD1(Resolvin D1) ELISA Kit
Reactivity:	Mouse
Alternative Names:	RvD1
Assay Type:	Competitive Inhibition
Sensitivity:	12.9 pg/mL
Standard:	2000 pg/mL
Detection Range:	31.25-2000 pg/mL
Sample type:	serum, plasma and other biological fluids
Assay length:	2.5h
Research Area:	Immunology & Inflammation
Test principle:	This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse RvD1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse RvD1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Mouse RvD1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
2000.00	0.185
1000.00	0.413
500.00	0.596
250.00	0.997
125.00	1.197
62.50	1.522
31.25	1.889
0.00	2.101

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 RvD1 and the recovery rates were calculated by comparing the measured value to the expected amount of RvD1 in samples.

Matrix	Recovery range	Average
serum(n=5)	84-106%	100%
EDTA plasma(n=5)	87-99%	93%
Heparin plasma(n=5)	87-93%	90%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of RvD1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.