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Screen Format

When you stop work, save your m-files in a folder, so you can use them next time. You can also save the workspace, which will save all the numerical values that have been calculated. This is convenient if you have to interrupt your work for a short time and do not want to start over. Of course, most of your work is contained in your m-files, which you always want to save. [Pg.240]

If a simulation continues for a long time and you want to halt it, press Control-1-Break or Control-I-C on the PC or Control- -C on the Macintosh. This will stop the program as a forced quit. [Pg.240]

In MATLAB you write computer programs that are called m-files and are saved on your computer. The files can be used at any time by simply typing their name in the command line, and one m-file can use another m-file. You will want to include comments in your m-file that explain what the file does. This is done by inserting a % everything after % on a line is considered a comment. These comments remind you of details when you come back to the program at a later time. [Pg.241]


Tracks air pollution emissions. Screen formats for data input and output in Basic. User can customize using Basic. [Pg.282]

Screen formating Models need to be positioned on screen in the way they are to appear in Spartan View. Any graphical surfaces and maps that are to be available to Spartan View need to be displayed. (These will not be displayed upon opening of the SpARTANView screen.)... [Pg.287]

ReproducibiUty in a primary HTS even with a good a/ (quality metric) >0.5 is an issue [9]. The concordance in a tripUcate HTS with identical target, identical screening format and identical compounds seldom exceeds 65%. Problems persist post primary HTS. IC50 rankings and selectivity panels can be seriously flawed if nominal rather than actual concentration is used. AH competent drug discovery... [Pg.262]

Schullek JR, Butler JH, Ni ZJ, Chen D, Yuan ZY, A high-density screening format for encoded combinatorial libraries assay miniaturization and its application to enzymatic reactions, Anal. Biochem., 246 20-29, 1997. [Pg.232]

Batch Executed Semi-Automated Screen Format.190... [Pg.183]

Plants are not different from other natural product samples in that they too tend to interfere with various screening formats in nonspecific ways as nuisance compounds displaying unwanted color, inherent fluorescence, promiscuous or aggregate behaviors, detergent-like activities, or toxicity (Feng et al., 2005 Appleton, Buss, and Butler, 2007). Biochemical assays (cell-free defined systems) are notoriously sensitive to such interference by natural product extracts. Cell-based reporter assays and cell-based so-called phenotypic screens always require parental cell controls to determine extract toxicity. However, plants contain their own sets of components that are problematic to screening assays and compound identification. [Pg.215]

From a purely biological perspective, data analysis of small molecules and natural product screening differ only slightly. Certain screen formats such as enzyme-based screens are vulnerable to interference by extracts and can exhibit high false positive rates. The ability to flag troublesome extracts is vital to allow the identification of genuine active samples. Conversely, the identification of false negatives is afflicted by the very complex natures of natural products due to their inherent properties and extraction methods. [Pg.219]

Kolb, J.M. and Manly, S.P. 1997. Adaptation of time-resolved fluorescence to homogeneous screening formats. In Janzen, B., Ed. High-Throughput Screening The Discovery of Bioactive Substances, New York Marcel Dekker, pp. 377-388. [Pg.231]

Menu/display hierarchy Display structure Screen formats Screen access security Toolbar options Message bars... [Pg.717]

This can also be a problem when you have carefully laid out a screen format with blanks or boxes into which a user is supposed to enter information. You have no way to control... [Pg.46]

Press the 1 key to enter new questions and create a quiz. You ll then be asked if a file of quiz names exists. If this is the first time you ve used the program or if you re starting a new group of tests on a new disk, answer by hitting N. Next, provide a name for your quiz. The quiz name is stored in a SEQuential file called TEST TITLES. Quiz Generator accepts up to 15 quiz files for each disk (a limitation because of the menu s screen formatting). If you re covering more than one subject, you may want to have a separate disk for each—for... [Pg.90]

When you return to the menu, type 2 to review the questions. The screen formatting section of the program right justifies your questions, and the screen display ends each line with the last word which fits without hyphenation. [Pg.91]

The ability to run assays that require a separation step becomes limited as assay volumes are reduced in higher density array plates. Therefore, mix-and-read or homogeneous screening formats are essential to miniaturization, requiring only a series of additions to perform the screen. Examples of homogeneous assay formats that have been developed for low volume screens include prompt fluorescence, FRET including time-resolved FRET, fluorescence polarization, and laser scanning fluorimetry. [Pg.43]


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