Irisin ELISA Assay Kit
The Irisin ELISA Assay Kit is For Research Use Only
Size: 1×96 wells
Sensitivity: 6.8 ng/ml
Dynamic Range: 0.1-1000 ng/mL
Incubation Time: 5 hours
Sample Type: Serum, Plasma
Sample Size: 50 µL
Alternative Name: Multispecies Irisin ELISA
Cross Reactivity
The cross-reactivity with the following factors were as below:
Irisin (Human, Rat, Mouse): 100%
Irisin (aa. 42-112) (Human, Rat, Mouse): 100%
Irisin precursor, C-terminal 48mer/ FNDC5 (aa. 149-196) (Human)/ FNDC5 (aa. 162-209) (Rat, Mouse): 0%
Irisin (aa. 42-95) (Human, Rat, Mouse): 0%
Assay Principle
This is a Competitive Enzyme Immunoassay for the quantification of Irisin in Serum and plasma samples This assay employs the competitive enzyme immunoassay technique. A secondary antibody has been pre-coated onto a microtiter plate and nonspecific binding sites were blocked. Fc regions of primary antibodies specific for target peptides can bind to the secondary antibodies on microtiter plate. The Fab regions of primary antibodies are competitively bound by biotinylated peptide and targeted peptides in samples or standards. The biotinylated peptide interacts with streptavidin-horseradish peroxidase (SA-HRP) which catalyzes the substrate solution. The reaction is monitored by a color change which is readable at OD of 450 nm±2 nm. Quantification of unknown samples is achieved by comparing their absorbance with a reference curve prepared with known standards. The intensity of color development is inversely proportional to the amount of Irisin in the samples.
Related Products
High Sensitive Irisin ELISA
Human Prolactin ELISA Assay
Glucagon ELISA Assay Kit
Assay Background
This gene encodes a secreted protein that is released from muscle cells during exercise. The encoded protein may participate in the development of brown fat. Translation of the precursor protein initiates at a non-AUG start codon at a position that is conserved as an AUG start codon in other organisms. Alternative splicing results in multiple transcript variants. Irisin: mediates beneficial effects of muscular exercise. Induces browning of white adipose tissue by stimulating UCP1 expression, at least in part, via the nuclear receptor PPARA.
Assay Procedure
1. Add 50 μl of 1X assay buffer as Total Binding. Keep another Two Empty Wells as Blank.
2. Add 50 μl of peptide standards (1000 ng/ml, 100 ng/ml, 10 ng/ml, 1 ng/ml and 0.1 ng/ml), 50 μl positive controls or 50 μl samples into corresponding wells. It is advisable to assay each condition in duplicates.
3. Add 25 μl of primary antibody into each well except the Blank wells.
4. Add 25 μl of Biotinylated peptide into each well except the Blank wells. It is not recommended to use a multi-channel pipette to load the primary antibody and biotinylated peptide.
5. Seal the microtiter plate with acetate plate sealer (APS). Incubate for 2 hours at room temperature (20-23°C). Orbital shaking at 300-400 rpm with a microplate shaker is recommended.
6. Centrifuge Streptavidin-HRP vial to spin down the solution in the vial and pipette 12 μl of Streptavidin-HRP into 12ml of 1X Assay buffer. Vortex thoroughly. Prepare fresh.
7. Remove sealer from plate.
8. Aspirate each well and wash, repeating the process 3 times for a total 4 washes. Wash by filling each well with 1× Assay Buffer (350 μl) using a squirt bottle, manifold dispenser, or autowasher. Complete removal of liquid at each is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating, decanting or blotting against clean paper towels.
9. Add 100 μl diluted Streptavidin-HRP solution into each well.
10. Reseal the plate with sealer. Incubate for 1 hour at room temperature (20- 23°C). Orbital shaking at 300-400 rpm with a microplate shaker is recommended.
11. Remove sealer from plate.
Package Inserts
Please note: All documents above are for reference use only and should not be used in place of the documents included with this physical product. If digital copies are needed, please contact us.
