久久精品国产久精国产AV_人紅細胞生成素(EPO)酶聯(lián)免疫吸附檢測試劑盒-科鹿（武漢）生物科技有限責任公司

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人紅細胞生成素(EPO)酶聯(lián)免疫吸附檢測試劑盒

ELK1011

規格：	價(jià)格：
48T	￥1680.00
96T	￥2400.00

下載說(shuō)明 ①

Overview 文獻

Product name:	Human EPO(Erythropoietin) ELISA Kit
Reactivity:	Human
Alternative Names:	EP; Epoetin; Erythropoetin; Hematopoietin; Hemopoietin
Assay Type:	Sandwich
Sensitivity:	11.5 pg/mL
Standard:	2000 pg/mL
Detection Range:	31.25-2000 pg/mL
Sample Type:	serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length:	3.5h
Research Area:	Cytokine;Endocrinology;Hematology;Hormone metabolism;
Uniprot ID:	P01588
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 EPO. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human EPO. 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 EPO, 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 EPO in the samples is then determined by comparing the OD of the samples to the standard curve.

Naunyn-Schmiedeberg's Archives of Pharmacology

Impact of Calcium Channel Blockers and Angiotensin Receptor Blockers on Hematological Parameters in Type 2 Diabetic Patients

日期：2023-09-20 IF：3.6

標準曲線(xiàn)

Concentration (pg/mL)	OD	Corrected OD
2000.00	2.258	2.192
1000.00	1.563	1.497
500.00	0.908	0.842
250.00	0.571	0.505
125.00	0.295	0.229
62.50	0.179	0.113
31.25	0.120	0.054
0.00	0.066	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 EPO and the recovery rates were calculated by comparing the measured value to the expected amount of EPO in samples.

Matrix	Recovery range	Average
serum(n=5)	81-95%	88%
EDTA plasma(n=5)	83-97%	90%
Heparin plasma(n=5)	87-95%	91%

線(xiàn)性

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