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人前腦源性神經(jīng)營(yíng)養(yǎng)因子(ProBDNF)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK8417

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

下載說(shuō)明 ①

Overview 文獻(xiàn)

Product name:	Human ProBDNF(Pro Brain Derived Neurotrophic Factor) ELISA Kit
Reactivity:	Human
Alternative Names:	Neurotrophin; Abrineurin
Assay Type:	Sandwich
Sensitivity:	6.3 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;Infection immunity;Neuro science;
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 ProBDNF. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ProBDNF. 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 ProBDNF, 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 ProBDNF in the samples is then determined by comparing the OD of the samples to the standard curve.

Scientific Reports

Alcohol use disorder disrupts BDNF maturation via the PAI-1 pathway which could be reversible with abstinence

日期：2024-09-29 IF：3.8

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
1000.00	1.842	1.753
500.00	1.507	1.418
250.00	1.279	1.190
125.00	0.887	0.798
62.50	0.594	0.505
31.25	0.355	0.266
15.63	0.208	0.119
0.00	0.089	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 ProBDNF and the recovery rates were calculated by comparing the measured value to the expected amount of ProBDNF in samples.

Matrix	Recovery range	Average
serum(n=5)	83-99%	95%
EDTA plasma(n=5)	94-105%	98%
Heparin plasma(n=5)	82-94%	88%

線性

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