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Assay number

Oseltamivir carboxylate 18 is used in sialidase inhibition assays Numbering used is that of A/N2 Abed et al. (2008)... [Pg.142]

Figure 6.4 Raw image data from four-analyte human IgG subclass assay. Numbers beside microarray rows indicate expected concentration of each subclass in the four-component myeloma mixture assayed in a given image. (From Silzel, J.W. et al., Clin. Chem., 44, 2036-2043, 1998. With permission.)... Figure 6.4 Raw image data from four-analyte human IgG subclass assay. Numbers beside microarray rows indicate expected concentration of each subclass in the four-component myeloma mixture assayed in a given image. (From Silzel, J.W. et al., Clin. Chem., 44, 2036-2043, 1998. With permission.)...
Number of samples tested in the Abbott, Beckman, Dade-Behring, OCD, and Roche assays. Number of samples tested in die Tosoh assay. [Pg.1639]

Assay Number Analyst Log10 Transformed Estimates Sample Absorbance Cut Point... [Pg.231]

Assay Number Analyst r o o Transformed Estimates Absorbance Multiplicative Normalization Factor... [Pg.232]

End-group assay Number of end groups in polymeric chains 2x 10 ... [Pg.115]

Methods to Detect and Quantitate Viral Agents in Fluids. In order to assess the effectiveness of membrane filtration the abihty to quantitate the amount of vims present pre- and post-filtration is critical. There are a number of techniques used. The method of choice for filter challenge studies is the plaque assay which utilizes the formation of plaques, localized areas in the cell monolayer where cell death caused by viral infection in the cell has occurred on the cell monolayer. Each plaque represents the presence of a single infectious vims. Vims quantity in a sample can be determined by serial dilution until the number of plaques can be accurately counted. The effectiveness of viral removal may be determined, as in the case of bacterial removal, by comparing the vims concentration in the input suspension to the concentration of vims in the effluent. [Pg.143]

The General Tests and Assays. This section of the USP gives methods for tests that are general in nature and apply to a number of the substances. Procedures are iacluded for such tests as heavy metals, melting point, chloride, sulfate, sterility, bacterial endotoxins, and pyrogens. Also iacluded are descriptions of various analytical techniques, such as spectrophotometry, chromatography, and nmr, and descriptions of tests to be used on glass or plastic containers, mbber closures, etc. [Pg.445]

Process Design and Machinery. Following the field work of geologists and mining engineers and analyses (assays) to estabhsh the grades (concentrations) of values in ores, a mineral concentration flow sheet is estabhshed on the basis of a number of preliminary tests. These include studies of... [Pg.41]

Sample and status tracking Database searches Numbers of samples assayed Tests utilised... [Pg.517]

Biomedical Applications. TRIS AMINO is used for a number of purposes in its pure form, it is an acidimetric standard the USP grade can be utilized intraveneously for therapeutic control of blood acidosis TRIS AMINO also is useful in genetic engineering as a buffering agent for enzyme systems, industrial protein purification, and electrophoresis. AMP has found use as a reagent in enzyme-linked immunoassays. The primary appHcation is for alkaline phosphatase assays. [Pg.19]

Name CAS Registry Number Molecular formula Molecular weight Physical form at 25°C Boiling point, Freezing point, °C Density, g/mL Typical Assay Flash point, °C Molten color APHA... [Pg.58]

The amino group is readily dia2oti2ed in aqueous solution, and this reaction forms a basis for the assay of sulfas. Aldehydes also react to form anils, and the yellow product formed with 4-(dimethylamino)hen2a1dehyde can be used for detection in thiu-layer and paper chromatography. Chromatographic retention values have been deterrnined in a number of thiu layer systems, and have been used as an expression of the lipophilic character of sulfonamides (23). These values have corresponded well with Hansch lipophilic parameters determined in an isobutyl alcohol—water system. [Pg.466]

The dehydrogenation of the mixture of m- and -ethyltoluenes is similar to that of ethylbenzene, but more dilution steam is required to prevent rapid coking on the catalyst. The recovery and purification of vinyltoluene monomer is considerably more difficult than for styrene owing to the high boiling point and high rate of thermal polymerization of the former and the complexity of the reactor effluent, which contains a large number of by-products. Pressures as low as 2.7 kPa (20 mm Hg) are used to keep distillation temperatures low even in the presence of polymerization inhibitor. The finished vinyltoluene monomer typically has an assay of 99.6%. [Pg.489]


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See also in sourсe #XX -- [ Pg.61 , Pg.62 , Pg.63 , Pg.394 , Pg.395 , Pg.396 , Pg.397 ]




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Assay number basic data

Reliability assay number

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