產(chǎn)品中心

人P物質(zhì)(SP)酶聯(lián)免疫吸附檢測試劑盒

ELK1039

規(guī)格：	價格：
48T	￥1680.00
96T	￥2400.00

下載說明 ①

Overview 文獻(xiàn)

Product name:	Human SP(Substance P) ELISA Kit
Reactivity:	Human
Alternative Names:	Substance P
Assay Type:	Sandwich
Sensitivity:	5.24 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:	Endocrinology;Neuro science;Hormone metabolism;
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 SP. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SP. 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 SP, 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 SP in the samples is then determined by comparing the OD of the samples to the standard curve.

Journal of Clinical and Diagnostic Research

Substance P Level in Patients with Degenerative Lumbar Spine Disorder undergoing Decompressive Surgery: An Observational Study.

日期：2024-06-01 IF：0.2

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
1000.00	2.270	2.201
500.00	1.529	1.460
250.00	0.885	0.816
125.00	0.495	0.426
62.50	0.266	0.197
31.25	0.163	0.094
15.63	0.118	0.049
0.00	0.069	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 SP and the recovery rates were calculated by comparing the measured value to the expected amount of SP in samples.

Matrix	Recovery range	Average
serum(n=5)	82-97%	90%
EDTA plasma(n=5)	88-106%	97%
Heparin plasma(n=5)	87-99%	93%

線性

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