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Human RANKL(Receptor Activator of Nuclear factor-kB Ligand) Microsample ELISA Kit
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ELK9869MS
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48 T $320.00
96 T $458.00
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Overview

Product name: Human RANKL(Receptor Activator of Nuclear factor-kB Ligand) Microsample ELISA Kit
Reactivity: Human
Alternative Names: CD254; TNFSF11; ODF; OPGL; TRANCE; HRANKL2; SOdf; Tumor Necrosis Factor(ligand)superfamily Member 11; TNF-related activation-induced cytokine; RANkL; Receptor Activator Of Nuclear Factor Kappa B Ligand
Assay Type: Sandwich
Sensitivity: 22.9 pg/mL
Standard: 5000 pg/mL
Detection Range: 78.13-5000 pg/mL
Sample Type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length: 3.5h
Research Area: Signal transduction;Metabolic pathway;Apoptosis;Tumor immunity;Bone metabolism;
Uniprot ID: O14788
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 RANKL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human RANKL. 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 RANKL, 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 RANKL in the samples is then determined by comparing the OD of the samples to the standard curve.

Standard curve

Concentration (pg/mL) OD Corrected OD
5000.00 1.990 1.898
2500.00 1.539 1.447
1250.00 1.086 0.994
625.00 0.732 0.640
312.50 0.523 0.431
156.25 0.321 0.229
78.13 0.230 0.138
0.00 0.092 0.000

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 RANKL and the recovery rates were calculated by comparing the measured value to the expected amount of RANKL in samples.
Matrix Recovery range Average
serum(n=5) 92-107% 100%
EDTA plasma(n=5) 92-97% 95%
Heparin plasma(n=5) 92-105% 99%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of RANKL 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) 86-93% 89-116% 82-110% 89-117%
EDTA plasma(n=5) 92-111% 86-113% 90-105% 90-103%
Heparin plasma(n=5) 85-110% 81-117% 80-118% 85-110%

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