產(chǎn)品詳情
簡單介紹:
HumanCytokineArrayC11
詳情介紹:
Purpose | C-Series Human Cytokine Antibody Array 11 Kit. Detects 37 Human Cytokines. Suitable for all liquid sample types. |
Sample Type | Plasma, Cell Culture Supernatant, Serum, Cell Lysate, Tissue Lysate |
Analytical Method | Semi-Quantitative |
Detection Method | Chemiluminescent |
Specificity | 2B4 (CD244), ADAM-9, APRIL, BMP-2, BMP-9, Cathepsin L, CD200, CD97, Chemerin, C5a, DcR3, FABP2, FAP, FGF-19, Galectin-3, HGFR, IFN-alpha / beta R2, IGF-2 R, IL-1 R6 (IL-1 Rrp2), IL-24, IL-33 (IL-1 F11), Kallikrein 14, Legumain, LOX-1, MBL, Neprilysin, Notch-1, NOV (CCN3), Osteoactivin (GPNMB), PD-1, PGRPs, SERPINA4, sFRP-3, Thrombomodulin, TLR2, Transferrin, WIF-1 |
Characteristics |
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Components |
Antibody Array Membranes Biotinylated Detection Antibody Cocktail Blocking Buffer Wash Buffers 1 and 2 Cell & Tissue Lysis Buffer Detection Buffers C and D Plastic Incubation Tray Protease Inhibitor Cocktail (in select kits) |
Material not included |
Pipettors, pipet tips and other common lab consumables Orbital shaker or oscillating rocker Tissue Paper, blotting paper or chromatography paper Adhesive tape or Saran Wrap Distilled or de-ionized water A chemiluminescent blot documentation system (such as UVP's ChemiDoc-It? or EpiChem II Benchtop Darkroom), X-ray Film and a suitable film processor, or another chemiluminescent detection system. |
Application Notes |
Perform ALL incubation and wash steps under gentle rotation or rocking motion (~0.5 to 1 cycle/sec) using an orbital shaker or oscillating rocker to ensure complete and even reagent/sample coverage. Rocking/rotating too vigorously may cause foaming or bubbles to appear on the membrane surface which, should be avoided. All washes and incubations should be performed in the Incubation Tray (ITEM 10) provided in the kit. Cover the Incubation Tray with the lid provided during all incubation steps to avoid evaporation and outside debris contamination. Ensure the membranes are completely covered with sufficient sample or reagent volume during each incubation. Avoid forceful pipetting directly onto the membrane, instead, gently pipette samples and reagents into a corner of each well. Aspirate samples and reagents completely after each step by suctioning off excess liquid with a pipette. Tilting the tray so the liquid moves to a corner and then pipetting is an effective method. Optional overnight incubations may be performed for the following step to increase overall spot signal intensities: - Sample Incubation - Biotinylated Antibody Cocktail Incubation - HRP-Streptavidin Incubation |
Comment |
The C-Series arrays feature chemiluminescent signal detection. The antibodies are spotted on nitrocellulose membrane solid supports and are handled in a very similar manner to Western blots. |
Sample Volume | 1 mL |
Plate | Membrane |
Protocol |
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Restrictions | For Research Use only |
Handling Advice | The antibody printed side of each membrane is marked by a dash (-) or number (#) in the upper left corner. Do not allow membranes to dry out during the experiment or they may become fragile and break OR high and/or uneven background may occur. Grasp membranes by the corners or edges only using forceps. DO NOT touch printed antibody spots. |
Storage | -20 °C |
Storage Comment | For best results, store the entire kit frozen at -20°C upon arrival. Stored frozen, the kit will be stable for at least 6 months which is the duration of the product warranty period. Once thawed, store array membranes and 1X Blocking Buffer a -20°C and all other reagents undiluted at 4°C for no more than 3 months. |
Supplier Images |
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