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大鼠神經(jīng)元特異性烯醇化酶(NSE)酶聯(lián)免疫吸附檢測試劑盒
ELK2589
規(guī)格: 價(jià)格:
48T ¥1960.00
96T ¥2800.00

Overview 文獻(xiàn)

Product name: Rat NSE(Enolase, Neuron Specific) ELISA Kit
Reactivity: Rat
Alternative Names: ENO2; Enolase 2; Gamma Enolase; 2-phospho-D-glycerate hydro-lyase; Neural enolase
Assay Type: Sandwich
Sensitivity: 0.237 ng/mL
Standard: 40 ng/mL
Detection Range: 0.63-40 ng/mL
Sample Type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length: 3.5h
Research Area: Enzyme & Kinase;Tumor immunity;Infection immunity;Neuro science;
Uniprot ID: P07323
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 Rat NSE. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NSE. 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 Rat NSE, 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 Rat NSE in the samples is then determined by comparing the OD of the samples to the standard curve.

標(biāo)準(zhǔn)曲線

Concentration (ng/mL) OD Corrected OD
40.00 2.054 1.958
20.00 1.636 1.540
10.00 1.128 1.032
5.00 0.901 0.805
2.50 0.567 0.471
1.25 0.312 0.216
0.63 0.179 0.083
0.00 0.096 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 NSE and the recovery rates were calculated by comparing the measured value to the expected amount of NSE in samples.
Matrix Recovery range Average
serum(n=5) 91-99% 95%
EDTA plasma(n=5) 82-95% 88%
Heparin plasma(n=5) 83-98% 91%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of NSE and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Matrix 1:2 1:4 1:8 1:16
serum(n=5) 88-97% 79-92% 85-93% 89-97%
EDTA plasma(n=5) 85-94% 87-96% 79-95% 95-102%
Heparin plasma(n=5) 95-102% 97-105% 92-101% 85-92%
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