Assay-kits

SensoLyte® Anti-MOG(35-55) IgG Quantitative ELISA Kit (mouse/rat) Colorimetric - 1 kit

582.00
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  • Cat.Number : AS-54465
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    In stock
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MOG peptide fragment (35-55) [Cat# AS-60130] induces autoantibody production and relapsing-remitting neurological disease causing extensive plaque-like demyelination. Autoantibody response to MOG (35-55) is present in multiple sclerosis (MS) patients and MOG (35-55)-induced experimental autoimmune encephalomyelitis (EAE) mice.
The SensoLyte® Anti-MOG (35-55) IgG Quantitative ELISA Kit (mouse/rat) provides a convenient, quantitative assay for detecting anti-MOG (35-55) IgG. This colorimetric assay, useful for determining the amount of anti-MOG (35-55) IgG present, can help provide information on the role anti-MOG (35-55) IgG plays in the development of EAE, an in vivo animal model for MS pathogenesis. The assays are performed in a convenient 96-well (strips format).

Specifications

Packaging
Kits components
  • Component A: MOG (35-55) coated and BSA blocked 8-well strips: 12 strips. Component B: Mouse anti-MOG (35-55) IgG standard: 110 µl (5 µg/ml). Component C: 1X Sample Dilution Buffer: 30 ml. Component D: 10X Wash Buffer: 50 ml. Component E: TMB color substrate solution: 10 ml. Component F: Stop Solution: 10 ml. Component G: Secondary antibody, Goat anti-Mouse IgG-HRP: 30 µl. Component H: Secondary antibody, Goat anti-Rat IgG-HRP: 30 µl. Component J: Rat anti-MOG (35-55) IgG standard: 110 µl (5 µg/ml)
Chemistry
UniProt number
  • Q61885, Q63345
Storage & stability
Storage Conditions
  • Store all components at 4°C for up to 6 months. Components B and J must be stored at -20 °C in small aliquots. Protect components E, G, and H from light.
Activity
Application
Biomarker Target
Detection Method
Detection Limit
  • 1 ng/ml
Research Area
Sub-category Research Area
Usage
  • Research use
Codes
Code Nacres
  • NA.32

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Citations

Cerebrospinal fluid dendritic cells infiltrate the brain parenchyma and target the cervical lymph nodes under neuroinflammatory conditions

PLoS ONE . 2008 Oct 02 ; 3 e3321 | DOI : 10.1371/journal.pone.0003321

  • E. Hatterer
  • et al