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Glutaraldehyde Solution

Harvested samples should be immediately prepared for the SEM by fixation in a 0.5% osmium tetroxide solution in the dark for 1 h. If the sample is collected in the field, store in buffered 3% glutaraldehyde solution (pH 7.2) until samples can be fixed. [Pg.203]

Diatom colonies formed in polystyrene culture dishes were fixed by adding a 2.5% glutaraldehyde solution to culture dish. [Pg.203]

Dextrose Solution Glutaraldehyde Solution Glycerine Tannic Acid Glycerine... [Pg.54]

Glutaraldehyde Solution Acetylacetone N-Amyl Mercaptan N-Amyl Alcohol Pentaerythritol 1-Pentene Amyl Acetate N-Amyl Alcohol Ethyl Butanol N-Amyl Chloride N-Amyl Methyl Ketone N - Amyltrochlorosilane Peracetic Acid Urea Peroxide Perchloric Acid Perchloric Acid... [Pg.74]

Aldehydes Acetaldehyde Acrolein (inhibited) Butyraldehyde Dec aldehyde Ethylhexald ehyde Formaldehyde Glutaraldehyde Solution Glyoxal Solution Methylbutyraldehyde Octyl Aldehyde Pentyl Aldehyde Propionaldehyde Valeraldehyde... [Pg.273]

Glutaraldehyde Solution — Fire Hazards Flash Point (deg. F) Non flammable solution ... [Pg.374]

Ruijgrok, J. M., Boon, M. E., and de Wijn, J. R. 1990. The effect of heating by microwave irradiation and by conventional heating on the aldehyde concentration in aqueous glutaraldehyde solutions. Histochem. J. 22 389-393. [Pg.338]

Equipment used in medical practice for disease diagnosis, which come into contact with the body, must be sterilized. Nonsterilizations can cause transmission of infection from one person to other. Commonly, 2% glutaraldehyde solution is used. Instruments must be kept in the solution for at least 3 hours, but high-level disinfection is achieved in 20 to 30 minutes for most. Glutaraldehyde is an irritant and may cause sensitization. Alternatively, paracetic acid, chlorine dioxide, and superoxidized water are used for this purpose. [Pg.310]

Introduction of the Glutaraldehyde Spacer. The y-amino-propyltrimethoxysilane modified surface was treated with 5% v/v aqueous glutaraldehyde solution. The reaction was performed at ambient temperature for 24 hours. The film was washed with water and dried. [Pg.65]

Glutaraldehyde solution Make a 2.5% solution of glutaraldehyde by diluting 25% stock solution 1/10 with PBS. This solution should be prepared fresh each time. [Pg.182]

Add 2.5% glutaraldehyde solution to the Petri dish, (1 mL to 3-cm dishes, 5 mL to 6-cm dishes) and leave for 10 min. Note All manipulations involving gluteraldehyde should be carried out in a fume hood. [Pg.186]

Enzyme membrane patterning procedures were utilized similar to the monofunctional FET biosensors, except that the membranes were developed in water instead of a glutaraldehyde solution. The center FET element was used as a reference FET employing a bovine serum albumini-immobilized membrane. After the three membranes were deposited on the FET surface, they were cross-linked by immersing them in a glutaraldehyde solution to make them mechanically strong. [Pg.173]

Place the F(ab )2 solution on magnetic stirrer and add 0.4 ml of glutaraldehyde solution dropwise from a Pasteur pipette. [Pg.123]

Dissolve 10 mg of peroxidase in 0.2 ml of a freshly prepared 1 25 dilution of the stock glutaraldehyde solution in phosphate buffer and allow to stand at room temperature for 18 hr. [Pg.133]

The beads of calcium alginate gel containing BLs were prefixed with 2% glutaraldehyde solution in 0.1 M Cacodylate buffer. [Pg.477]

Enzyme-collagen membranes have also been prepared by a simple casting method. A collagen fibril suspension containing enzyme In the pH range 4 to 5 Is cast on a Teflon plate at 4 C to form a membrane and dried at room temperature. The membrane Is then dipped In lZ(wt/vol) glutaraldehyde solution at pH 7. [Pg.450]


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