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小鼠巨噬細(xì)胞炎性蛋白1α(MIP1a)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK1116

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

下載說明 ①

Overview 文獻(xiàn)

Product name:	Mouse MIP1a(Macrophage Inflammatory Protein 1 Alpha) ELISA Kit
Reactivity:	Mouse
Alternative Names:	MIP1 Alpha; CCL3; MIP1-A; SCYA3; Chemokine C-C-Motif Ligand 3; Small Inducible Cytokine A3; Homologous To Mouse Mip-1a; Tonsillar Lymphocyte LD78 Alpha Protein
Assay Type:	Sandwich
Sensitivity:	5.9 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:	Cytokine;Infection immunity;
Uniprot ID:	P10855
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 Mouse MIP1a. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse MIP1a. 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 Mouse MIP1a, 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 Mouse MIP1a in the samples is then determined by comparing the OD of the samples to the standard curve.

iScience

Behenic acid alleviates inflammation and insulin resistance in gestational diabetes mellitus by regulating TLR4/NF-κB signaling pathway

日期：2024-10-18 IF：4.6

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
1000.00	2.354	2.281
500.00	1.790	1.717
250.00	0.915	0.842
125.00	0.505	0.432
62.50	0.340	0.267
31.25	0.230	0.157
15.63	0.116	0.043
0.00	0.073	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 MIP1a and the recovery rates were calculated by comparing the measured value to the expected amount of MIP1a in samples.

Matrix	Recovery range	Average
serum(n=5)	95-107%	101%
EDTA plasma(n=5)	90-105%	97%
Heparin plasma(n=5)	78-90%	84%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of MIP1a and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.