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人核因子κB亞基p105(NFKB-p105)微量上樣酶聯(lián)免疫吸附檢測試劑盒
一鍵復(fù)制產(chǎn)品信息
ELK2228MS
規(guī)格: 價(jià)格:
48T ¥1960.00
96T ¥2800.00
96T*5 ¥11900.00

Overview

Product name: Human NF-κBp105(Nuclear factor NF-kappa-B p105 subunit) Microsample ELISA Kit
Reactivity: Human
Alternative Names: NF-KB1; EBP-1; KBF1; NF-Kappa-B; NFKB-P105; NFKB-P50; Nuclear Factor Of Kappa Light Polypeptide Gene Enhancer In B-Cells 1; Nuclear factor NF-kappa-B p105 subunit; NFkB; Nuclear Factor Kappa B
Assay Type: Sandwich
Sensitivity: 0.058 ng/mL
Standard: 10 ng/mL
Detection Range: 0.16-10 ng/mL
Sample Type: tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length: 3.5h
Research Area: Signal transduction;
Uniprot ID: P19838
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 NF-κBp105. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NF-κBp105. 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 NF-κBp105, 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 NF-κBp105 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
10.00 2.189 2.108
5.00 1.566 1.485
2.50 1.128 1.047
1.25 0.824 0.743
0.63 0.516 0.435
0.31 0.320 0.239
0.16 0.155 0.074
0.00 0.081 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 NF-κBp105 and the recovery rates were calculated by comparing the measured value to the expected amount of NF-κBp105 in samples.
Matrix Recovery range Average
serum(n=5) 80-109% 95%
EDTA plasma(n=5) 88-123% 106%
Heparin plasma(n=5) 85-91% 88%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of NF-κBp105 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) 85-91% 87-118% 89-102% 83-110%
EDTA plasma(n=5) 95-109% 94-102% 93-117% 80-95%
Heparin plasma(n=5) 85-113% 94-116% 80-102% 80-112%

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