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PCR,

Some methods that paitly cope with the above mentioned problem have been proposed in the literature. The subject has been treated in areas like Cheraometrics, Econometrics etc, giving rise for example to the methods Partial Least Squares, PLS, Ridge Regression, RR, and Principal Component Regression, PCR [2]. In this work we have chosen to illustrate the multivariable approach using PCR as our regression tool, mainly because it has a relatively easy interpretation. The basic idea of PCR is described below. [Pg.888]

It may look weird to treat the Singular Value Decomposition SVD technique as a tool for data transformation, simply because SVD is the same as PCA. However, if we recall how PCR (Principal Component Regression) works, then we are really allowed to handle SVD in the way mentioned above. Indeed, what we do with PCR is, first of all, to transform the initial data matrix X in the way described by Eqs. (10) and (11). [Pg.217]

The profits from using this approach are dear. Any neural network applied as a mapping device between independent variables and responses requires more computational time and resources than PCR or PLS. Therefore, an increase in the dimensionality of the input (characteristic) vector results in a significant increase in computation time. As our observations have shown, the same is not the case with PLS. Therefore, SVD as a data transformation technique enables one to apply as many molecular descriptors as are at one s disposal, but finally to use latent variables as an input vector of much lower dimensionality for training neural networks. Again, SVD concentrates most of the relevant information (very often about 95 %) in a few initial columns of die scores matrix. [Pg.217]

Sections 9A.2-9A.6 introduce different multivariate data analysis methods, including Multiple Linear Regression (MLR), Principal Component Analysis (PCA), Principal Component Regression (PCR) and Partial Least Squares regression (PLS). [Pg.444]

The goal of PCR is to extract intrinsic effects in the data matrix X and to use these effects to predict the values of Y. [Pg.448]

PCR is a combination of PCA and MLR, which are described in Sections 9.4.4 and 9.4.3 respectively. First, a principal component analysis is carried out which yields a loading matrix P and a scores matrix T as described in Section 9.4.4. For the ensuing MLR only PCA scores are used for modeling Y The PCA scores are inherently imcorrelated, so they can be employed directly for MLR. A more detailed description of PCR is given in Ref. [5. ... [Pg.448]

The selection of relevant effects for the MLR in PCR can be quite a complex task. A straightforward approach is to take those PCA scores which have a variance above a certain threshold. By varying the number of PCA components used, the... [Pg.448]

This enzyme Is widely distributed, more particularly in plants. Three important sources of the enzyme are horse-radish, turnips and milk. Peroxidase is capable of activating both hydrogen peroxide and a suitable substrate so that the latter is oxidised, although hydrogen peroxide alone may be incapable of affecting this change. It sometimes happens that hydrogen pcr-... [Pg.521]

PCR can also be used to modify DNA sequences using primers differing at one or several positions from the target sequence. This is possible because PCR does not require perfect complementarity of a primer to the sequence flanking the target. Since all of the PCR products contain the primer sequence, an insertion or deletion can thus be incorporated into the product by modifying a primer. It is also possible to add new sequences to the 5 -ends of the primers. Modified or additional genetic information may thus be multiplied and transr ported. [Pg.227]

The mam use of PCR is to amplify or make hundreds of thousands—even mil lions—of copies of a portion of the polynucleotide sequence m a sample of DNA Sup pose for example we wish to copy a 500 base pair region of a DNA that contains a total of 1 million base pairs We would begin as described m Section 28 14 by cleaving the DNA into smaller fragments using restriction enzymes then use PCR to make copies of the desired fragment... [Pg.1183]

All of the substances necessary for PCR are present throughout and proceeding from one cycle to the next requires only changing the temperature after suitable time inter vals The entire process is carried out automatically and 30 cycles can be completed within a few hours... [Pg.1183]

PCR IS reviewed in the April 1993 issue of the Journal of Chemical Education pp 273-280 A PCR experi ment suitable for under graduate laboratories appears in the April 1994 issue pp 340-341... [Pg.1183]

FIGURE 28 14 The poly merase chain reaction (PCR) Three cycles are shown the target region appears after the third cycle Additional cycles lead to amplification of the target region... [Pg.1184]

Distribution of DNAs with Increasing Number of PCR Cycles... [Pg.1185]

More recently PCR proved to be a valuable detection and analytical tool during the terrorist inspired anthrax outbreak m the fall of 2001... [Pg.1186]

Cobalt difluoride, used primarily for the manufacture of cobalt trifluoride, CoF, is available from Advance Research Chemicals, Inc., Aldrich Chemicals, and PCR in the United States, Fluorochem in the UK, and Schuhardt in Germany. The 1993 price varied from 60 to 200/kg depending on the quantity and the price of cobalt metal. C0F2 is shipped as a corrosive and toxic material in DOT-approved containers. [Pg.178]

In spite of the many appHcations for copper(II) fluoride, demand is restricted to 1 to 10 kg lots. It is available ia the United States from Advance Research Chemicals, Aldrich Chemicals, Atomergic, Aesar, Johnson/Matthey, Cerac Corp., and PCR Corp. The 1993 price for the anhydrous copper(II) fluoride varied from 400 to 600/kg depending on the amount required. The dihydrate is available at 22/kg. [Pg.180]

The only reported industrial appHcation for Fep2 is its use in mst removal solutions based on oxalic acid (6). The anhydrous salt is commercially available in 100 g to 5 kg lots from Advance Research Chemicals, Aldrich Chemicals, Cerac, Johnson/Matthey, PCR, and other suppHers in the United States. As of 1993, the prices varied between 500 to 700/kg. [Pg.202]

Mercury(II) fluoride has been used in the process for manufacture of fluoride glass (qv) for fiber optics (qv) appHcations (11) and in photochemical selective fluorination of organic substrates (12). It is available from Advance Research Chemicals, Aldrich Chemicals, Johnson/Matthey, Aesar, Cerac, Strem, and PCR in the United States. The 1993 annual consumption was less than 50 kg the price was 800—1000/kg. [Pg.210]

Historically, the annual consumption of nickel fluoride was on the order of a few metric tons. Usage is droppiag because nickel fluoride is Hsted ia the EPA and TSCA s toxic substance iaventory. Nickel fluoride tetrahydrate is packaged ia 200—500-lb (90.7—227-kg) dmms and the 1993 price was 22/kg. Small quantities for research and pilot-plant work are available from Advance Research Chemicals, Aldrich Chemicals, Johnson/Matthey, Pfalt2 and Bauer, PCR, and Strem Chemicals of the United States, Fluorochem of the United Kingdom, and Morita of Japan. [Pg.214]

Uses. Silver fluoride has found many laboratory and special industrial appHcations. It is used as a soft (nHld) fluorinating agent for selective fluorination (7—17), as a cathode material in batteries (qv) (18), and as an antimicrobial agent (19). Silver fluoride is commercially available from Advance Research Chemicals, Inc., Aldrich Chemicals, Cerac Corp., Johnson/Matthey, PCR, Atochem, and other sources in the United States. The U.S. price of silver fluoride in 1993 was 1000— 1400/kg and the total U.S. consumption was less than 200 kg/yr. [Pg.235]

Inc., Allentown, Peimsylvania MarChem, Inc., Houston, Texas Ozark-Mahoning, Inc., Tulsa, Oklahoma and PCR, Inc., Gainesville, Florida. [Pg.278]


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Allele specific PCR

Amplification in PCR

Applications of PCR to agricultural biotechnology

Asymmetric PCR

Bases, Nucleosides, Nucleotides, Oligonucleotides, Nucleic Acids, and PCR Products

Basic principles of real-time PCR

Basic principles of the PCR

Biotinylated PCR products

Colony PCR

Competitive PCR

Continuous-flow PCR

Cytokine mRNA RT-PCR analysis

DNA Amplification by Polymerase Chain Reaction (PCR)

DNA and RNA sequences by the polymerase chain reaction (PCR)

Deoxyribonucleic acid profiling and PCR

Detection of T-DNA by Polymerase Chain Reaction (PCR)

Differential display PCR

Error-prone PCR

Exponential phase, of PCR

Extension PCR

Flow-Through PCR

Fusion PCR

Hot-Start PCR

Hybridization, PCR

Immuno-PCR

Immunocapture PCR

Integrated PCR-CE microdevice

Inverse PCR

Jumping PCR

Kinetic PCR

MPN-PCR

Micro-PCR devices

Microchip based PCR

Multiplex PCR

Mutagenesis and PCR

Mutagenic PCR

Mycoplasma Detection Methods using PCR

Nested PCR

Nucleic Acid Amplification - The Polymerase Chain Reaction (PCR)

One-Step RT-PCR

Optimization of PCR

Optimization of a PCR Reaction

PCA and PCR

PCR (polymerase chain

PCR , detection

PCR = polymerase chain reaction

PCR A Printing Press for Genes

PCR Calibration

PCR Lab-on-Chip Devices

PCR Prediction

PCR Product

PCR Product Polishing

PCR System Kit

PCR amplification reaction

PCR amplification techniques

PCR analysis

PCR and protein expression

PCR assay

PCR cloning

PCR contamination

PCR fingerprinting techniques

PCR for products of agricultural biotechnology

PCR in Action

PCR inhibitor

PCR labeling

PCR method

PCR mutagenesis

PCR process

PCR products analysis

PCR reverse transcription-polymerase chain

PCR techniques

PCR test

PCR, chamber

PCR, inhibition

PCR-DGGE

PCR-amplification

PCR-amplified

PCR-based analysis

PCR-based markers

PCR-based reverse genetics

PCR-denaturing gradient gel

PCR-denaturing gradient gel electrophoresis

PCR-mediated gene disruption

PCR-reaction

PCR/ESI

Polymerase Chain Reaction and Error-Prone PCR

Polymerase chain reaction (PCR amplification

Polymerase chain reaction PCR primers

Post-consumer recycled (PCR

Primary PCR of antibody genes

Primers, in PCR

Principal component regression (PCR

Principle of PCR

QIAquick PCR Purification Kit

QRT-PCR

Quantitative PCR

Quantitative polymerase chain reaction Q-PCR)

Quantitative real-time PCR

Quantitative reverse transcription PCR

RAPD-PCR

RT-PCR

RT-PCR (reverse

RT-PCR (reverse transcriptase

RT-PCR (reverse transcriptase-polymerase chain

RT-PCR (reverse transcription-polymerase

RT-PCR analyses

RT-PCR analyses of tumor necrosis factor TNF

RT-PCR products

RT-PCR reaction

Random amplified polymorphic DNA RAPD)-PCR

Random amplified polymorphic DNA-PCR

Reagents for PCR

Real-time PCR

Real-time PCR analysis

Real-time PCR applications

Real-time PCR assay

Real-time PCR instruments

Real-time PCR primer

Real-time PCR probes

Real-time RT-PCR

Real-time polymerase chain reaction RT-PCR)

Recursive PCR

Restriction fragment length polymorphism, PCR

Reverse transcriptase PCR

Reverse transcriptase-polymerase chain reaction RT-PCR)

Reverse transcription PCR

Reverse transcription PCR assays

Reverse transcription RT-PCR)

Reverse transcription polymerase chain reaction RT-PCR)

Sau-PCR

Sexual PCR

Single chain Fv antibodie jumping-PCR assembly

StEP PCR

Starting a PCR Reaction

Surface Passivation of PCR Chambers

The PCR Amplification Process

The Polymerase Chain Reaction (PCR)

The Principle of PCR

TruPoint®-PCR

Two-Step RT-PCR

What Is PCR

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