These Goat polyclonal antibodies are affinity purified and adsorbed against human proteins in order to avoid cross reactivity on human origin tissue. Depending of their labelling, they are suitable for use in: immunofluorescence, immunoperoxidase, western blot, flow cytometry, ELISA... In case blood cells are present in the studied specimens, preferably use F(ab’)2 fragment antibodies in order to avoid non specific binding due to Fc receptors. Recommended working dilutions: FITC-Microscopy: 1/50-1/250, HRP-Microscopy: 1/50-1/250, HRP-ELISA: 1/1000-1/5000, HRP-Blotting: 1/500-1/3000.

These Goat polyclonal antibodies are affinity purified and adsorbed against human proteins in order to avoid cross reactivity on human origin tissue. Depending of their labelling, they are suitable for use in: immunofluorescence, immunoperoxidase, flow cytometry... Recommended working dilutions: FITC-Microscopy: 1/50-1/250, HRP-Microscopy: 1/50-1/250.

This buffer is suitable for dilution and/or washing steps of almost all antibodies listed in this catalog (refer to products package insert). The fluorescence with Fluorescein Isothiocyanate labelled antibodies is maximized when the pH is slightly alkaline (pH 7.2). Reconstitution: Each vial contains sufficient powder for 1 liter of ready to use PBS. Use only distilled water for reconstitution. Composition For 1 liter: NaCl:7.650 g / Na2HPO4:724 g / KH2PO4: 0.210 g.

Provides red contrasting of cells in immunofluorescence. Reconstitution: Evans blue 1% is used in the range of 1/50 to 1/500 diluted in PBS (1/5 000-1/50 000 final).

Teflon coated slides 10 wells 6 mm diameter. These slides are suitable for use with acetone or methanol and for deep-freeze.

Buffered glycerol solution recommanded for the use of Argene monoclonal antibodies in immunofluorescence for mounting coverslips over microscope preparations

Gelatinous solution of polyvinylic alcohol, glycerol, and Tris buffer designed for fixing coverslips over microscopic preparation, particularly for Immunofluorescence. With FLUOKEEP™ the preparation can be stored without loss of fluorescence for a few days stored at +2/+8°C.

Single use 10 wells plastic slides to count the leukocytes before the cytocentrifugation in the CMV pp65 antigenemia technic.

This buffer is suitable for the coating of antibodies on plastic (microplates, beads). Each tablet is sufficient for 100 mL of ready to use buffer. Reconstitution: Each tablet is dissolved in 100 mL of distilled water.

This kit allows preparation of AEC substrate simply by mixing 1 drop of each of the 3 reagents in 1 mL of distilled water. This substrate will produce a red colored deposit upon reaction with peroxidase. Kit content: A. 1 dropper bottle (12 mL) of buffer concentrate (20x), B. 1 dropper bottle (12 mL) of chromogen concentrate (20x), C. 1 dropper bottle (12 mL) of concentrate hydrogen peroxide (20x). Preparation of substrate / chromogen mixture: To 1 mL of distilled water add 1 drop of reagent A (mix well), 1 drop of reagent B, 1 drop of reagent C (mix again). The substrate/chromogen mixture is ready to use. This solution should be kept away from light and used within 30 min. Recommended guidelines for use: Incubate the substrate/chromogen mixture with the specimen for 3-5 mn. If desired incubation times up to 30 mn can be done with satisfactory results. Color development may be monitored under a microscope. After the color is adequately developed, the specimen may be counterstained and mounted with an aqueous or permanent mounting solution.