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Sample labels

Table 7.9 lists the estimated fractions of dyads of types m and r and the fractions of triads of types i, s, and h. These fractions represent the area under a specific peak (or four peaks in the case of the meso dyads) divided by the total area under all of the peaks in either the dyad or triad category. As expected for the sample labeled isotactic, 89% of the triads are of type i and 87% of the dyads are of type m. Likewise, in the sample labeled syndiotactic, 68% of the triads are s and 83% of the dyads are r. [Pg.484]

The sample labeled atactic in Fig. 7.10 was prepared by a free-radical mechanism and, hence, is expected to follow zero-order Markov statistics. As a test of this, we examine Fig. 7.9 to see whether the values of p, P, and Pj, which are given by the fractions in Table 7.9, agree with a single set of p values. When this is done, it is apparent that these proportions are consistent with this type... [Pg.484]

Adequate pre-shop provision, thorough training, and strict oversight of the shoppers, as described above, were critical to the successful execution of the sample collection phase of the OPMBS. Each shopper received a kit containing sample labels and containers to hold the sampled commodities, ice packs and packaging materials, labels and boxes for use in shipping the collected commodities, written instructions, and forms well before the scheduled date of collection. The sample coordinator monitored sample collection and advised shoppers of actions to take when problems inevitably arose. [Pg.241]

Thereafter, the primary functions of the study QA specialist fell into two main headings. First, GLP compliance during the collection and documentation of commodity samples had to be assured. This was done via observation of several collections for different shops (collection incidents) at various geographic locations. In these audits, the study QA specialist examined specific items, such as (1) did the shopper follow the written instructions, (2) were the correct types and numbers of samples collected, (3) was the documentation maintained as required, (4) were the samples labeled and packaged correctly, and (5) were the samples delivered to the shipper as required Findings were communicated to study management and used as appropriate in subsequent shops. [Pg.246]

Label sample bottles prior to sample collection and always double check the label prior to collecting a sample. All sample labels should include the study number... [Pg.807]

Innovatory boronated carbons (manufactured in the Institute of Chemistry and Technology of Petroleum and Coal, Wroclaw University of Technology, Poland) were obtained by co-pyrolysis of coal-tar pitch with a pyridine-borane complex. In the first stage of pyrolysis (520°C) the so-called semi-coke is obtained. Further carbonization at 2500°C leads to obtaining boron-doped carbonaceous material (sample labeled 25B2). [Pg.208]

Fig. 22. Arhennius plot of the hydrogen diffusion coefficient for n-type a—Si=H (HT 4[PH3]/SiH4]), comparing the fast diffusing component in columnar material with data for a noncolumnar sample (labeled normal) (Street and Tsai, 1988). Fig. 22. Arhennius plot of the hydrogen diffusion coefficient for n-type a—Si=H (HT 4[PH3]/SiH4]), comparing the fast diffusing component in columnar material with data for a noncolumnar sample (labeled normal) (Street and Tsai, 1988).
All rules pertaining to scientific notebooks are applicable to held notebooks and must be followed. Every entry must be dated and each sample labeled with their associated description in the book. No removed pages, no erasures, and no sections whited out are allowed. Sections may be crossed out if necessary, but in a manner in which the words can still be read. [Pg.157]

DR. WILLIAM TROGLER (Northwestern University) You looked at exchange between the monohydride anion of osmium and the neutral dihydride. Have you ever studied the bimolecular self-exchange for a neutral dihydride This could be followed by mixing one sample labelled with deuterium and one with hydrogen. [Pg.418]

Figure 4.19. Torsion constant a versus buffer concentration for supercoiled M13mp7 DNA in different buffers. All samples except that in 10 mM Tris contain 10 raW NaCl, so all have between 10 and 12 mM univalent positive ions. The sample in the middle contains only 10 mM NaCl. The numbers (1, 2, and 4) in the sample label refer to the gel electrophoretic mobilities, which reflect different tertiary structures, as described in the text. The a samples all contain varying amounts of Tris, while the b samples all contain citrate. Figure 4.19. Torsion constant a versus buffer concentration for supercoiled M13mp7 DNA in different buffers. All samples except that in 10 mM Tris contain 10 raW NaCl, so all have between 10 and 12 mM univalent positive ions. The sample in the middle contains only 10 mM NaCl. The numbers (1, 2, and 4) in the sample label refer to the gel electrophoretic mobilities, which reflect different tertiary structures, as described in the text. The a samples all contain varying amounts of Tris, while the b samples all contain citrate.
FIGURE 3 CE-SDS separations of non-reduced and reduced preparations of rMAb control samples labeled with 5-TAMRA SE, and a sample that exhibited evidence of a microbial infection during cell culture fermentation. The arrows indicate the appearance of new peaks in the infected rMAb samples. (Reprinted from reference 11, with permission.)... [Pg.406]

A limitation of the flow cytometric binding assay has been the precise determination of the receptor affinity and calculation of the receptors per cell. This limitation appears to have been overcome by the development of fluorescein and phycoerythrin compensation-calibration standards (Flow Cytometry Standards Corp., Research Triangle Park, NC). These standards have made it possible to quantify the fluorescence intensity of samples labeled with fluorescein or phycoerythrin, and relate the intensity to molecules of equivalent soluble fluorochrome. These standards have been utilized in quantitative studies of neutrophil chemoattractant-ligand interaction (4). [Pg.307]

Test results can be displayed and printed either by patient or test with cumulative storage. Patient data are automatically stored until specifically deleted. The Patient Identifier function permits accurate sample labelling and identification. [Pg.41]

Several samples labelled as undiscriminated samples on the binary plots are widely scattered on figure 1. Most of these samples were collected from areas adjacent to chemostratigraphic contacts. The spurious nature of these data may reflect the effect of mixed-source sampling. [Pg.279]

Two aspects of Q.C. sample labelling require discussion. 1) Which sample should be "A" and which "B" 2) Should samples be analyzed "blind" Labelling samples "A" and "B" is merely an operational convenience. The labels are only used to prepare Q.C. plots and compute sums, differences, and statistics. If the first Q.C. [Pg.259]

In terms of test substances, reagents, and samples, the QAU would want to look in the notebooks or logbooks to see if these substances are properly identified. It would also want to look at the container labels for proper identification (identity, concentration, composition, storage requirements, and expiration date). It would want to take note of expiration dates to see if all test substances and reagents are current. It would look for proper storage of substances, chain-of-custody documentation (date, quantity, distributor, receiver, etc.), and sample labels to see if they are adequate to avoid mixups. [Pg.72]

The sample tubes should be numbered consecutively from 1 up. Any plot codes, identifying letters, etc., should be kept by the person submitting the samples for later interpretation. This simplifies the sample labelling and record... [Pg.24]

Scores Plot (Sample Diagnostic) The score plot of score 2 vs. score 1 is shown in Figure 4.87, with the samples labeled with the corresponding concentrations. The scores on the first PC are related to concentration (the score value increases as the concentration increases) but there is no strong dependence with respect to score 2. This supports a one-component PCA model as being appropriate. [Pg.268]

Stores receiving labels are hxed on all containers and sample labels are affixed as appropriate. [Pg.142]

The samples collected can either be assayed individually or combined, and then a subset of the gross sample is assayed as depicted in Figure 1 and described below. Sample increments should be combined on a clean, dry surface or in a suitable container or bag. All containers that the sample comes into contact with should be inert and not chemically or physically react with the sample. In addition, accurate sample labeling and records must be kept. If the sample is divided, then the retained portion should be kept for possible future analysis and labeled with at least the date, gross field sample number, lot number, and/or reference number from bill of lading. The material to be tested should be labeled with at least the date, gross field sample... [Pg.400]


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See also in sourсe #XX -- [ Pg.47 ]




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