Human IL-16 ELISA Kit
Size: 96T
Range: 31.2 pg/ml - 2000 pg/ml
Sensitivity < 5 pg/ml
Application: For quantitative detection of IL-16 in human serum, plasma, body fluids, tissue lysates or cell culture supernatants.
--------------------------------------------------------------------------------------------------------------
Price: $360.00
Catalog No.: BEK1304
Size: 96T
Range: 31.2 pg/ml - 2000 pg/ml
Sensitivity < 5 pg/ml
Storage and Expiration: Store at 2-8℃ for 6 months, or at -20℃ for 12 months.
Application: For quantitative detection of IL-16 in human serum, plasma, body fluids, tissue lysates or cell culture supernatants.
Introduction
Interleukin 16 is a pro-inflammatory pleiotropic cytokine. Its precursor, pro-interleukin-16 is a protein that in humans is encoded by the IL16 gene. The cytokine encoded by this gene is a pleiotropic cytokine that functions as a chemoattractant, a modulator of T cell activation, and an inhibitor of HIV replication. The signaling process of this cytokine is mediated by CD4. The product of this gene undergoes proteolytic processing, which is found to yield two functional proteins. The cytokine function is exclusively attributed to the secreted C-terminal peptide, while the N-terminal product may play a role in cell cycle control. Caspase 3 is reported to be involved in the proteolytic processing of this protein. Two alternatively spliced transcript variants encoding distinct isoforms have been reported.
Principle of the Assay
This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti- IL-16 polyclonal antibody was pre-coated onto 96-well plates. And the biotin conjugated anti- IL-16 polyclonal antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and wash with wash buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the IL-16 amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of IL-16 can be calculated.
Kit components
- One 96-well plate pre-coated with anti-human IL-16 antibody
- Lyophilized human IL-16 standards: 2 tubes (10ng / tube)
- Sample / Standard diluent buffer: 30ml
- Biotin conjugated anti-human IL-16 antibody (Concentrated): 130μl. Dilution: 1:100
- Antibody diluent buffer: 12ml
- Avidin-Biotin-Peroxidase Complex (ABC) (Concentrated): 130μl. Dilution: 1:100
- ABC diluent buffer: 12ml
- TMB substrate: 10ml
- Stop solution: 10ml
- Wash buffer (25X): 30ml
- Note: Reconstitute standards and test samples with Kit Component 3.
Material Required But Not Provided
- 37℃ incubator
- Microplate reader (wavelength: 450nm)
- Precise pipette and disposable pipette tips
- Automated plate washer
- ELISA shaker
- 1.5ml of Eppendorf tubes
- Plate cover
- Absorbent filter papers
- Plastic or glass container with volume of above 1L