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大鼠α1-酸性糖蛋白(a1AGP)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK5247

規(guī)格：	價(jià)格：
48T	￥1960.00
96T	￥2800.00

下載說(shuō)明 ①

Overview 文獻(xiàn)

Product name:	Rat a1AGP(Alpha-1-Acid Glycoprotein) ELISA Kit
Reactivity:	Rat
Alternative Names:	alpha1-AGP; AGP1; a1-AGP; ORM1; OMD 1; Orosomucoid 1
Assay Type:	Sandwich
Sensitivity:	2.88 ng/mL
Standard:	400 ng/mL
Detection Range:	6.25-400 ng/mL
Sample Type:	serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length:	3.5h
Research Area:	Infection immunity;Hepatology;Gastroenterology;Immunodeficiency;
Uniprot ID:	P02764
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 a1AGP. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat a1AGP. 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 a1AGP, 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 a1AGP in the samples is then determined by comparing the OD of the samples to the standard curve.

The Journal of Infectious Diseases

The Efficacy and Safety of an Intra-articular Dual-Acting Antibacterial Agent (TNP-2092) for Implant Infection–Associated Methicillin-Resistant Staphylococcus aureus

日期：2023-12-26 IF：3.2

標(biāo)準(zhǔn)曲線

Concentration (ng/mL)	OD	Corrected OD
400.00	2.172	2.089
200.00	1.694	1.611
100.00	1.196	1.113
50.00	0.782	0.699
25.00	0.555	0.472
12.50	0.336	0.253
6.25	0.199	0.116
0.00	0.083	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 a1AGP and the recovery rates were calculated by comparing the measured value to the expected amount of a1AGP in samples.

Matrix	Recovery range	Average
serum(n=5)	80-95%	87%
EDTA plasma(n=5)	81-95%	88%
Heparin plasma(n=5)	87-99%	93%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of a1AGP and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.