- Size
- 8 Sample Kit
- Species
- Human
- Compatible Sample Types
- Cell Culture Supernatants, Plasma, Serum, Tissue Lysates, Cell Lysates
- Quantitative/Semi-Quantitative
- Semi-Quantitative
- Number of Targets Detected
- 507
- Solid Support
- Glass Slide
- Design Principle
- Label-based
- Method Of Detection
- Fluorescence Laser Scanner
- Research Area
- Post-Translational Modifications, Oxidative Stress
- Introduction
- Protein Oxidation has been linked to aging, cancer and other diseases. The Human Protein Oxidation Antibody Array 1 is specifically designed for simultaneous identification of the relative levels of oxidation of 507 different human proteins in cell lysate, culture supernatant, serum, plasma and other biological samples. By monitoring the changes in protein oxidation in your experimental model system, you can verify oxidative damage without spending excess time and effort performing an analysis of immunoprecipitation and/or Western Blot. The Human Protein Oxidation Antibody Arrays utilizes the 'biotin probes' method to biotin label carbonyl groups of oxidized proteins. In this method, the biotin probes first react with carbonyl groups of oxidized proteins to form the unstable Schiff bases, which are then further reduced to more stable amines. The biotin labeled sample then is added into antibody array glass slide wells. The antibody array slide wells are washed. After incubation with a fluorescent dye-conjugated streptavidin (Cy3 equivalent), the slides can then be imaged using a laser scanner, such as the Axon GenePix, using the Cy3 channel.
- Product Features
- High sensitivity and specificity;Low sample volume (10-100 µl per array);Large dynamic range of detection;Compatible with most sample types;Test 4 or 8 samples on each slide;Suitable for high-throughput assays
- Suggested Application
- Multiplexed Protein Detection; Detection of Relative Protein Expression; Detecting Patterns of Cytokine Expression; Biomarker Screening; Identifying Key Factors; Confirming a Biological Process
- Kit Components
- Glass Slide(s);Blocking Buffer;Fluorescent Dye-Conjugated Streptavidin (Cy3 equivalent);20X Wash Buffer I Concentrate;20X Wash Buffer II Concentrate;Wash Buffer III;2X Cell Lysis Buffer Concentrate;Protease Inhibitor Cocktail;Oxidation Buffer A;Oxidation Labeling Reagent;Oxidation Stabilizing Reagent;Centrifugal Filter Unit;Adhesive film
- Other Materials Required
- 20% (v/v) trichloroacetic acid (TCA) solution, ice‑cold;1:1 (v/v) ethanol:ethyl acetate;Desalting column or dialysis membrane;1.5 mL microcentrifuge tubes;15 mL tubes (polypropylene);<10 mL graduated cylinders (X2);Benchtop centrifuge and microcentrifuge (4°C);Precision pipettes to deliver 2 µl to 1 ml volumes;Adjustable 1‑25 ml pipettes for reagent preparation;Water bath or heat block;Shaker;Laser scanner for fluorescence detection;Aluminum foil;Distilled water;Plastic box;50 ml Centrifuge tube;Isopropanol (2‑propanol)
- Protocol Outline
- 1.Dry the Glass Slide;2.Blocking and Incubation;3.Fluorescence Detection
- Storage/Stability
- Upon receipt, the kit should be stored at ≤-20°C. Please use within 6 months from the date of shipment.