Mouse IL23 Single Analyte ELISArray Kit
SEM03763A
Applications
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Pathway
Apoptosis
Biomarkers
Cell Cycle
Cytokine & Inflammation
ECM & Adhesion
Neuroscience
Signal Transduction
Stem Cell & Development
Toxicology & Drug ADME
Diseases
Cancer
Cardiovascular Diseases
CNS Disorders
Immune Disorders
Infectious Diseases
Metabolic Diseases
 
Description
The Mouse IL23 Single Analyte ELISArray Kit is designed to quantitatively measure the amount of this cytokine in cell culture supernatant, serum or plasma using a conventional enzyme-linked immunosorbent assay (ELISA). Each 96-well plate (8 wells/strip, 12 strips) is coated with the protein-specific capture antibody. We screened all commercially available antibodies to identify the best capture and detection antibodies. The high sensitivity, good linearity and low background of the Single Analyte ELISArray Kits provide reliable and reproducible results for your cytokine and chemokine analyses.
Product Resources
Pricing and Ordering Related Array Products Assemble Your Own ELISArray
More information on IL23 from Wikipedia:
"IL-23 is an important part of the inflammatory response against infection. It promotes upregulation of the matrix metalloprotease MMP9, increases angiogenesis and reduces CD8+ T-cell infiltration. Recently, IL-23 has been implicated in the development of cancerous tumors. In conjunction with IL-6 and TGF-β1, IL-23 stimulates naive CD4+ T cells to differentiate into a novel subset of cells called Th17 cells, which are distinct from the classical Th1 and Th2 cells. Th17 cells produce IL-17, a proinflammatory cytokine that enhances T cell priming and stimulates the production of proinflammatory molecules such as IL-1, IL-6, TNF-alpha, NOS-2, and chemokines resulting in inflammation. Knockout mice deficient in either p40 or p19, or in either subunit of the IL-23 receptor (IL-23R and IL12R-β1) develop less severe symptoms of multiple sclerosis and inflammatory bowel disease highlighting the importance of IL-23 in the inflammatory pathway."
Kit Contents / Storage Conditions/ Shelf Life
Please check the kit components immediately after you receive this package. SuperArray is only responsible for missing items reported within two (2) business days of receipt.

Enough reagents are provided to process the included plate of 12 ELISA strips.

Component / Description  Quantity
BOX 1: Shipped on blue ice packs. Store at -20 ºC.
Antigen Standard (1 mg/ml)  1.5-ml tube
Detection Antibody  1.5-ml tube
Avidin-HRP Conjugate  1.5-ml tube
10% BSA  15 ml bottle
Donkey Serum  15 ml bottle
BOX 2: Shipped at ambient temperature. Store at 4 ºC.
Pre-coated Capture Antibody 8-well strips  One plate of 12 strips in a pouch
Sample Dilution Buffer Stock  60 ml bottle
Assay Buffer Stock  60 ml bottle
Wash Buffer (10X Concentrate)  125 ml bottle
Development Solution  60 ml bottle
Stop Solution  60 ml bottle

Storage Conditions: All reagents are stable at the recommended temperature for 6 months after receipt of the kit. Do not use kit beyond the expiration date printed on the label.

Brief Protocol
The Brief Protocol is meant for experience users only. First-time users should refer to the User Manual.
  1. Prepare replicate serial dilutions of the Antigen Standard and your experimental samples.
  2. Pipette 50 µl of Assay Buffer into each well of the 8-well ELISA strips.
  3. Transfer 50 µl samples and/or standards to the appropriate wells of the ELISA strips.
  4. Gently shake or tap plate for 10 s. Incubate for 2 h at room temp.
  5. Washing ELISA Wells:
    Decant or aspirate well contents. Add 350 µl 1X Washing Buffer. Gently shake or tap plate for 10 s. Decant or aspirate. Blot array upside down on absorbent paper to remove any residual buffer. Repeat wash twice more.
  6. Pipette 100 µl of Detection Antibody solution. Incubate 1 h at room temp.
  7. Wash ELISA wells as described above.
  8. Add 100 µl Avidin-HRP solution to all wells. Incubate for 30 min at room temp.
  9. Wash ELISA wells for a total of 4 washes.
  10. Add 100 µl of Development Solution to each well. Incubate the plate for 15 min at room temp in the dark.
  11. Add 100 µl of Stop Solution to each well. The color changes from blue to yellow.
  12. Read absorbance at 450 nm within 30 min of stopping the reaction. If wavelength correction is available, subtract readings at 570 nm from the reading at 450 nm.
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