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Stains hands

Potassium permanganate, approximately saturated solution - (Note wear rubber gloves to prevent staining hands.) dissolve 50 g KMnO in I I water (solubility = 65 g at 20°C). Store in a brown glass bottle. [Pg.126]

Caution. Toxic and stains hands, clothing, and other things on prolonged contact. The free base of p-phenylenediamine and its water soluble salts may cause eczema or other skin irritations. Always wear a good dust mask when working with the powder and gloves when working with the powder or the solutions. [Pg.185]

Cardiovascular Effects. Elevated pulse rates have been observed in humans exposed to DNOC by inhalation. A male factory worker who had been employed for 17 days pouring DNOC powder had a pulse rate of 130 beats per minute (Hunter 1950). Although his yellow- stained hands and feet indicated dermal exposure, he reported that he had periodically inhaled DNOC aerosols. A pulse rate of 100 beats per minute, a blood pressure of 155/70 mm Hg, and a normal electrocardiogram were found for an employee who was involved with mixing DNOC, refilling sprayer tanks with DNOC, and occasionally spraying DNOC for 5 weeks (Pollard and Filbee 1951). The patient s clinical history also suggested that exposure was probably a combination of inhalation and dermal. [Pg.19]

Apart from the sheer complexity of the static stmctures of biomolecules, they are also rather labile. On the one hand this means that especial consideration must be given to the fact (for example in electron microscopy) that samples have to be dried, possibly stained, and then measured in high vacuum, which may introduce artifacts into the observed images [5]. On the other, apart from the vexing question of whether a protein in a crystal has the same stmcture as one freely diffusing in solution, the static stmcture resulting from an x-ray diffraction experiment gives few clues to the molecular motions on which operation of an enzyme depends [6]. [Pg.2815]

The apphcation of stains to substrates includes spray, flow, dip, roU-coat, or hand appHcation, ie, bmsh or rag methods. The type of appHcation method used depends on the function of the stain itself as well the type of product being manufactured. [Pg.337]

Pad stains are divided into two groups spray pads and hand pads. The difference between them, not surprisingly, can only be defined by the means of apphcation. Like the shade stains, they are usually appHed over the sealer or first topcoat and subsequendy are topcoated themselves. [Pg.339]

Silicones. SUicones are exceeded only by fluorochemicals in the volume used as repeUents for textiles. They are widely used on ceUulosic and synthetic fiber fabrics. SUicones provide water-based stain resistance good durabUity to washing improved tear strength a soft, sUck hand and improved fabric sewabUity. [Pg.308]

Detector tube kits generally include a hand pump that draws a known volume of air through a chemically treated tube intended to react with certain contaminants. The length of color stain resulting in the tube correlates to chemical concentration. [Pg.239]

In general, grafting of hydrophillic monomers have been found to lead to an increase in wettability, adhesion, dyeing, and rate of release of oil stains by detergent solution. On the other hand, if the monomer is hydro-phobic, the result will be decreased wetting by all liquids including oil stains. If grafting is not restricted to surface alone but encompasses the bulk of the backbone polymer, then the properties such as flame resistance, water sorption, crease resistance, etc. will be affected. [Pg.497]

Penetration of rust through an otherwise intact paint film is usually a result of inadequate surface preparation before painting, especially over weathered and hand-cleaned steel. However, superficial rust staining may be traceable to dissolved iron salts, e.g. in bilge water from a ship s deck. [Pg.607]

Figure 52-3. Diagrammatic representation of the major proteins of the membrane of the human red blood cell separated by SDS-PAGE. The bands detected by staining with Coomassie blue are shown in the two left-hand channels, and the glycoproteins detected by staining with periodic acid-Schiff (PAS) reagent are shown in the right-hand channel. (Reproduced, with permission, from Beck WS, Tepper Ri Hemolytic anemias iii membrane disorders, in Hematology, 5th ed. Beck WS [editor]. The MiT Press, 1991.)... Figure 52-3. Diagrammatic representation of the major proteins of the membrane of the human red blood cell separated by SDS-PAGE. The bands detected by staining with Coomassie blue are shown in the two left-hand channels, and the glycoproteins detected by staining with periodic acid-Schiff (PAS) reagent are shown in the right-hand channel. (Reproduced, with permission, from Beck WS, Tepper Ri Hemolytic anemias iii membrane disorders, in Hematology, 5th ed. Beck WS [editor]. The MiT Press, 1991.)...
The proglottid is examined under a dissecting microscope or with a hand lens, and the uterine branching is observed. Glycerine and beechwood creosote can also be used with good results. Cleared proglottids may be mounted or stained if desired. [Pg.25]

The staining of flagella is a difficult technique, especially in the hands of the beginner. For this reason many methods have been proposed. Regardless of the method employed, the film must first be treated with a mordant to make the flagella take the stain heavily. Mordants consist usually of a mixture of tannic acid and some metallic... [Pg.97]

Figure 16.1 Montage of images, after immunostaining of peptides. The antibody clones for these analytes are D07 (p53), 9C2 (HER2), 1D5 (ER), and 636 (PR). The peptides were spotted in duplicate, adjacent to each other. The left-hand column ( Not Fixed ) illustrates stained peptide spots that were not fixed, representing a baseline condition. The middle column was fixed in formalin and not antigen retrieved. The peptides for p53 and HER2 lost immunoreactivity whereas the peptides for ER and PR continued to be immunoreactive. The right-hand column of peptide spots were both formalin fixed and antigen retrieved. Adapted with permission from Reference 16, 2004 American Society for Clinical Pathology. Figure 16.1 Montage of images, after immunostaining of peptides. The antibody clones for these analytes are D07 (p53), 9C2 (HER2), 1D5 (ER), and 636 (PR). The peptides were spotted in duplicate, adjacent to each other. The left-hand column ( Not Fixed ) illustrates stained peptide spots that were not fixed, representing a baseline condition. The middle column was fixed in formalin and not antigen retrieved. The peptides for p53 and HER2 lost immunoreactivity whereas the peptides for ER and PR continued to be immunoreactive. The right-hand column of peptide spots were both formalin fixed and antigen retrieved. Adapted with permission from Reference 16, 2004 American Society for Clinical Pathology.
FIG. 2. Confocal image of an isolated smooth muscle cell from guinea-pig ileum which has been permeabilized with staphylococcal os-toxin and incubated with 150 /iM Fluo-3 acid which stains the SR. The SR is predominantly localized to the periphery of this type of smooth muscle as seen on the left hand side where the image plane is through the centre of the cell, whereas an extensive network is seen where the image plane is adjacent to the plasma membrane as seen in the right hand portion of the cell. [Pg.260]

The medium for maceration (HC1 or NaOH) depends on the material and purpose of staining. If fresh material is at hand, NaOH is best. It keeps material at the proper pH even after washing a few times in water. It is very important to achieve a pH of 9.0-10.0 to obtain the proper fluorescence of callose after staining with aniline blue. [Pg.94]

Yet every part of the walnut is useful to people. The outer husk produces a dark reddish stain that is hard to remove from the hands of the person who opens the nut, and this pigment is widely used in dyes and wood stains. The inner shell is used as an abrasive to clean jet engines. And the meat of the nut is extensively used in cooking, ice cream, flavorings—and just eaten raw. [Pg.185]

One hour prior to installation of the test substance, both eyes of each rabbit are examined for signs of irritation and comeal defects with a hand-held slit lamp. All eyes are stained with 2.0% sodium fluorescein and examined to confirm the absence of comeal lesions. [Pg.375]


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See also in sourсe #XX -- [ Pg.310 ]




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