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ELK Biotechnology

ELK9785

Human SDMA(Symmetric dimethylarginine) ELISA Kit

Human SDMA(Symmetric dimethylarginine) ELISA Kit

Sensitivity

Human SDMA(Symmetric dimethylarginine) ELISA Kit

Overview

Product name: Human SDMA(Symmetric dimethylarginine) ELISA Kit
Reactivity: Human
Alternative Names: Symmetric dimethylarginine
Assay Type: Competitive Inhibition
Sensitivity: 0.119 nmol/mL
Standard: 20 nmol/mL
Detection Range: 0.32-20 nmol/mL
Sample Type: EDTA Plasma, Serum
Assay Length: 2h
Research Area: Signal transduction;Developmental science;Bone metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human SDMA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SDMA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 SDMA in the samples is then determined by comparing the OD of the samples to the standard curve.

Standard curve

Concentration (ng/mL) OD Corrected OD
20.00 0.197 —
10.00 0.357 —
5.00 0.651 —
2.50 0.878 —
1.25 1.225 —
0.63 1.592 —
0.32 1.877 —
0.00 2.123 —

Precision

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.

Recovery

Matrices listed below were spiked with certain level of recombinant SDMA and the recovery rates were calculated by comparing the measured value to the expected amount of SDMA in samples.
Matrix Recovery range Average
serum(n=5) 90-105% 97%
EDTA plasma(n=5) 89-103% 96%
Heparin plasma(n=5) 87-99% 93%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of SDMA 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) 85-96% 89-102% 98-102% 81-94%
EDTA plasma(n=5) 87-96% 97-105% 95-102% 81-92%
Heparin plasma(n=5) 85-94% 87-105% 92-101% 79-90%
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