Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Labeling choice

Generally, the knowledge of microenvironment effects greatly simplifies label choice. This is an advantage of organic dyes as the spectroscopic properties of many... [Pg.25]

Note far best results, individual reagents should be titrated before use. The quantities specified below, when possible, are for rou guidance only. The labelling suggested here is biotin but as an example only. See Section 4 for labelling choices. [Pg.317]

Am, H. J.S. Cleeve. 1971. A double-label choice test for the simultaneous determination of diet preference and ingestion by the aphid Amphorophora agathonica. Entomol. Exp. Appl. 14 377-387. [Pg.261]

Hie common acrylic ester monomers are combustible liquids. Commercially, acrylic monomers are shipped with DOT red labels in bulk quantities, tank cars, or tank tmcks. Mild steel is the usual material of choice for the constmction of bulk storage facilities for acrylic monomers. Moisture must be excluded to avoid msting of the tanks and contamination of the monomers. Copper or copper alloys must not be allowed to contact acrylic monomers intended for use in polymerization because copper is an inhibitor (67). [Pg.165]

The flavor chemist is responsible for the basic knowledge of sensory and appHcation properties of each of this large number of raw materials the large number of possible combinations of these items to produce specifically flavored finished compounds is readily apparent. It is not uncommon to develop a flavor that combines essential oils, plant extractive, fmit juices, and synthetics. The choice of materials depends on type of product, conditions of manufacture, labeling, and intended use. [Pg.15]

Commonly, a juice drink contains 10% fruit juice, which usually is a blend of several fruits. The 1990 Federal Nutrition and Labeling Act requites declaration of juice content so that the consumer can make a more informed choice (3). With cocktails and juice drinks, added sugars, acids, flavorings, colorings, and nutrients can be used to provide a wide variety of stable products of uniform quaUty. Because drinks requite less juice than 100% juice products, the drinks can be sold at a lower price. [Pg.575]

In the labeling market, hot melts provide the capability to bond non-porous films to plastic cans and bottles. Hot melt usage has grown with the prevalence of such plastic to plastic laminations. The choice of hot melts depends on the equipment, the substrates, whether the bottles are filled or unfilled, and any post-labeling processing (e.g. pasteurization, or heat shrinkage of the film). [Pg.747]

Decau.se its longer half-life and lower energy make it more convenient to handle, is replacing "" P as the radioactive tracer of choice in. sequencing by the Sanger method. "" S-ct-labeled deoxynucleotide analogs provide die. source for incorporating radioactivity into DNA. [Pg.357]

Theoreticians did little to improve their case by proposing yet more complicated and obviously unreUable parameter schemes. For example, it is usual to call the C2 axis of the water molecule the z-axis. The molecule doesn t care, it must have the same energy, electric dipole moment and enthalpy of formation no matter how we label the axes. I have to tell you that some of the more esoteric versions of extended Hiickel theory did not satisfy this simple criterion. It proved possible to calculate different physical properties depending on the arbitrary choice of coordinate system. [Pg.144]

The location of the primary dull characteristic is described in the fourth space. There are six choices cone, nose, taper, shoulder, gauge, and all areas. Figure 4-167 shows four possible fixed cutter bit profiles with the different areas labeled. It is recognized that there are profiles for which the exact boundaries between areas are debatable and for which certain areas may not even exist. Notice that in the bottom profile there is no taper area shown. However, using Figure 4-167 as a guide, it should be possible to clearly define the different areas on most profiles. [Pg.811]

While the rows and columns of A obviously depend on a particular choice of vertex labels, the generic structural j)roperties of G must remain invariant under a permutation of rows and columns. Much of this structural information can in fact be extracted from the spectrum of G the spectrum of a graph G,... [Pg.33]

The minor difference in form between L and L is due to our choice of er G 0,1 variables as opposed to S G +1,-1 variables. This particular form for V just happens to be more convenient to work with when using a variables. The reader is encouraged to retrace our steps using S inste2id of a variables and the same L as used in proving Theorem 5. How our variables are labeled obviously cannot affect the dynamics. [Pg.277]

Which liquid should be given Label No. 1, Label No. 2, Label No. 3 Explain how each type of measurement influenced your choices. [Pg.319]

I ordered a Pink Puppy from the specialty cocktail list, which was labeled Elixirs So Many Choices, So LittleTime. Who s in a hurry in Minneapolis Only your hormones, if you re single. [Pg.46]

The choice of a labeled compound, able to react with the active transition metal-carbon bond. This compound should have an inhibiting effect strong enough to result in completely stopping polymerization on its addition in a quantity comparable with that of the transition metal compound in the polymerization system. [Pg.196]

Fischer projection of acyclic form, 56-57 glycosides, 132-135 C-glycosyl compounds, 139-140 N-glycosyl derivatives, 137-139 glycosyl halides, 136-137 glycosyl residues, 125 isotopic substitution and isotopic labelling, 91 me so forms, 59 optical rotation, 59 parent structure choice, 53... [Pg.487]

Because the choice of designations of groups in the periodic table is currently in a state of flux, it was decided to conform to the practice of several leading inorganic texts. To avoid confusion an appropriately labeled periodic table is printed on the back endpaper. [Pg.23]

Adequate precision and accuracy are only likely to be achieved if some standardization procedure is employed and the nature of this, internal or external standards or the method of standard additions, needs to be chosen carefully. If internal standardization procedures are adopted then appropriate compound(s) must be chosen and their effect on the chromatographic and mass spectrometry methods assessed. The ideal internal standard is an isotopically labelled analogue of the analyte but, although there are a number of commercial companies who produce a range of such molecules, these are not always readily available. An analytical laboratory is then faced with the choice of carrying out the synthesis of the internal standard themselves or choosing a less appropriate alternative with implications on the accuracy and precision of the method to be developed. [Pg.270]

The tacit assumption above is that the monodromy matrix is defined with respect to the primitive unit cell, with sides (5v, 8fe) = (0,1) and (1, 0), because the twist angle that determines the monodromy is given by A9 = — (Sv/Sfe)j.. However, situations can arise where other choices are more convenient. For example, the energy levels within a given Fermi resonance polyad are labeled by a counting number v = 0,1,... and an angular momentum that takes only even or only odd values. Thus the convenient elementary cell has sides (8v, 8L) = (0,2) and (1, 0), and the natural basis, say, y, is related to the primitive basis, x, by... [Pg.54]

The turnover rate of a transmitter can be calculated from measurement of either the rate at which it is synthesised or the rate at which it is lost from the endogenous store. Transmitter synthesis can be monitored by administering [ H]- or [ " C]-labelled precursors in vivo these are eventually taken up by neurons and converted into radiolabelled product (the transmitter). The rate of accumulation of the radiolabelled transmitter can be used to estimate its synthesis rate. Obviously, the choice of precursor is determined by the rate-limiting step in the synthetic pathway for instance, when measuring catecholamine turnover, tyrosine must be used instead of /-DOPA which bypasses the rate-limiting enzyme, tyrosine hydroxylase. [Pg.82]

For human studies, the choice of stable isotopes is limited because radioisotopes are associated with ionization radiation and thus with some potential harmful effects for humans. Studying the bioavailability of compounds labeled with stable isotopes requires complex techniques such as gas chromatography coupled with mass spectrometry (GC-MS), liquid chromatography coupled with MS (LC-MS), and atmo-... [Pg.151]


See other pages where Labeling choice is mentioned: [Pg.16]    [Pg.16]    [Pg.2814]    [Pg.76]    [Pg.89]    [Pg.35]    [Pg.439]    [Pg.53]    [Pg.110]    [Pg.181]    [Pg.221]    [Pg.11]    [Pg.162]    [Pg.163]    [Pg.179]    [Pg.51]    [Pg.37]    [Pg.380]    [Pg.600]    [Pg.766]    [Pg.433]    [Pg.183]    [Pg.42]    [Pg.245]    [Pg.199]    [Pg.94]    [Pg.43]    [Pg.128]   
See also in sourсe #XX -- [ Pg.271 ]




SEARCH



Labels choice

© 2024 chempedia.info