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Registro Completo |
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Biblioteca(s): |
Embrapa Semiárido. |
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Data corrente: |
04/09/2007 |
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Data da última atualização: |
17/02/2009 |
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Autoria: |
STEPHENSON, F. H. |
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Título: |
Calculations in molecular biology and biotechnology: a guide to mathematics in the laboratory. |
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Ano de publicação: |
2003 |
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Fonte/Imprenta: |
Amsterdam: Academic Press, 2003. |
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Descrição Física: |
1 CD-ROM. |
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Idioma: |
Inglês |
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Conteúdo: |
Introduction, Significant Digits, Rounding Off Significant Digits in Calculations, Exponents and Scientific Notation, Expressing Numbers in Scientific Notation, Converting Numbers from Scientific Notation to Decimal Notation, Adding and Subtracting Numbers Written in Scientific Notation, Multiplying and Dividing Numbers Written in Scientific Notation, Metric Prefixes, Conversion Factors and Canceling Terms, Section 2: Solutions, Mixtures, and Media Introduction, Calculating Dilutions: A General Approach, Concentrations by a Factor of X, Preparing Percent Solutions, Diluting Percent Solutions, Moles and Molecular Weight: Definitions, Molarity, Diluting Molar Solutions, Converting Molarity to Percent, Converting Percent to Molarity, Normality, PH, pKa and the Henderson-Hasselbalch Equation, Section 3: Cell Growth The Bacterial Growth Curve, Manipulating Cell Concentration, Plotting OD550 versus Time on a Linear Graph, Plotting the Logarithm of OD550 vs Time on a Linear Graph, Logarithms, Sample OD550 Data Converted to Log Values, Plotting Log OD550 versus Time, Plotting the Log of Cell Concentration versus Time, Determining Log Values, Calculating Generation Time, Slope and Growth Constant, Generation Time, Plotting Cell Growth Data on a Semilog Graph, Plotting OD550 vs Time on a Semilog Graph, Estimating Generation Time from a Semilog Plot of OD550 vs Time, Plotting Cell Concentration versus Time on a Semilog Graph, Determining Generation Time Directly from a Semilog Plot of Cell Concentration vs Time, Plotting Cell Density versus OD550 on a Semilog Graph, The Fluctuation Test, Fluctuation Test Example, Variance, Measuring Mutation Rate, The Poisson Distribution, Calculating Mutation Rate by Using Poisson Distribution, Using a Graphical Approach to Calculate Mutation Rate from Fluctuation Test Data, Mutation Rate Determined by Plate Spreading, Measuring Cell Concentration in a Hemocytometer, Section 4: Working with Bacteriophage Introduction, Multiplicity of Infection, Probabilities and moi, Measuring Phage Titer, Diluting Bacteriophage, Measuring Burst Size, Section 5: Quantitation of Nucleic Acids, Quantitation of Nucleic Acids by UV Spectroscopy, Determining the Concentration of Double-Stranded DNA, Using Absorbance and an Extinction Coefficient to Calculate Double-Stranded DNA Concentration, Calculating DNA Concentration as a Millimolar (mM) Amount, Determining the Concentration of Single-Stranded DNA Molecules, Single-Stranded DNA Concentration Expressed in ?g/mL, Determining the Concentration of Large Molecular Weight Single-Stranded DNA, (ssDNA) in pmol/?L, Expressing ssDNA Concentration as a mM Amount, Oligonucleotide Quantitation, OD Units, Expressing an Oligonucleotide's Concentration in ?g/mL, Oligonucleotide Concentration Expressed in pmol/?L, Measuring RNA Concentration, Molecular Weight, Molarity, and Nucleic Acid Length, Estimating DNA Concentration on an Ethidium Bromide Stained Gel, Section 6: Labeling Nucleic Acids with Radioisotopes Introduction, Using Radioactivity - The Curie, Estimating Plasmid Copy Number, Labeling DNA by Nick Translation, Determination of Percent Incorporation of Radioactive Label , Calculating Specific Radioactivity of a Nick Translation Product, Random Primer Labeling of DNA, Random Primer Labeling - Percent Incorporation, Random Primer Labeling - Calculating Theoretical Yield, Random Primer Labeling - Calculating Actual Yield, Random Primer Labeling - Calculating SpecificActivity of the Product, Labeling 3' Termini with Terminal Transferase, 3'-End Labeling with Terminal Transferase -Percent Incorporation, 3'-End Labeling with Terminal Transferase - Specific Activity of the Product, cDNA Synthesis, First Strand cDNA Synthesis, Second Strand cDNA Synthesis, Homopolymeric Tailing, In vitro Transcription, Section 7: Oligonucleotide Synthesis Introduction, Synthesis Yield, Measuring Stepwise and Overall Yield by the DMT Cation Assay, Overall Yield, Stepwise Yield, Calculating Micromoles of Nucleoside Added at Each Base Addition Step, Section 8: The Polymerase Chain Reaction Introduction, Template and Amplification , Exponential Amplification, PCR Efficiency, Calculating the Tm of the Target Sequence, Primers, Primer Tm, Calculating Tm Based on Salt Concentration, G/C Content, and DNA Length, Calculating Tm Based on Nearest Neighbor Interactions, DNTPs, DNA Polymerase, Calculating DNA Polymerase's Error Rate, Quantitative PCR, Section 9: Recombinant DNA Introduction, Restriction Endonucleases, The Frequency of Restriction Endonuclease Cut Sites, Calculating the Amount of Fragment Ends, The Amount of Ends Generated by Multiple Cuts, Ligation, Ligation Using Lambda-Derived Vectors, Packaging of Recombinant Lambda Genomes, Ligation Using Plasmid Vectors, Transformation Efficiency Genomic Libraries: How Many Clones do You Need? , cDNA Libraries: How Many Clones is Enough? , Expression Libraries, Screening Recombinant Libraries by Hybridization to DNA Probes, Oligonucleotide Probes, Hybridization Conditions, Hybridization Using Double-Stranded DNA Probes, Sizing DNA Fragments by Gel Electrophoresis, Generating Nested Deletions Using Nuclease BAL 31, Section 10: Protein Introduction, Protein Quantitation by Measuring Absorbance at 280 nm, Using Absorbance Coefficients and Extinction Coefficients to Estimate Protein, Concentration, Relating Absorbance Coefficient to Molar Extinction Coefficient, Determining a Protein's Extinction Coefficient, Relating mg/mL Concentration to Molarity, Protein Quantitation Using A280 when Contaminating Nucleic Acids are Present, Protein Quantitation at 205 nm, Protein Quantitation at 205 nm when Contaminating Nucleic Acids are Present, Measuring Protein Concentration by Colorimetric Assay - The Bradford Assay, Using b-Galactosidase to Monitor Promoter Activity and Gene Expression, Assaying b-Galactosidase in Cell Culture, Specific Activity, Assaying b-Galactosidase from Purified Extracts, The CAT Assay, Calculating Molecules of CAT, Use of Luciferase in a Reporter Assay, In vitro Translation - Determining Amino Acid Incorporation, Section 11: Centrifugation Introduction, Relative Centrifugal Force (g Force, ) Converting g Force to rpm, Determining g Force and rpm by Use of a Nomogram, Calculating Sedimentation Times, Section 12: Forensic Science Introduction, Alleles and Genotypes, Calculating Genotype Frequencies, Calculating Allele Frequencies, The Hardy-Weinberg Equation and Calculating Expected Genotype Frequencies, The Chi-square Test: Comparing Observed to Expected Values, Sample Variance, Sample Standard Deviation, Pi: The Power of Inclusion, Pd: The Power of Discrimination, DNA Typing and a Weighted Average, The Multiplication Rule, Index MenosIntroduction, Significant Digits, Rounding Off Significant Digits in Calculations, Exponents and Scientific Notation, Expressing Numbers in Scientific Notation, Converting Numbers from Scientific Notation to Decimal Notation, Adding and Subtracting Numbers Written in Scientific Notation, Multiplying and Dividing Numbers Written in Scientific Notation, Metric Prefixes, Conversion Factors and Canceling Terms, Section 2: Solutions, Mixtures, and Media Introduction, Calculating Dilutions: A General Approach, Concentrations by a Factor of X, Preparing Percent Solutions, Diluting Percent Solutions, Moles and Molecular Weight: Definitions, Molarity, Diluting Molar Solutions, Converting Molarity to Percent, Converting Percent to Molarity, Normality, PH, pKa and the Henderson-Hasselbalch Equation, Section 3: Cell Growth The Bacterial Growth Curve, Manipulating Cell Concentration, Plotting OD550 versus Time on a Linear Graph, Plotting the Logarithm of OD550 vs Time on a Linear Graph, Logarithms, Sample OD550 Data Converted to Log Values, Plotting Log OD550 versus Time, Plotting the Log of Cell Concentration versus Time, Determining Log Values, Calculating Generation Time, Slope and Growth Constant, Generation Time, Plotting Cell Growth Data on a Semilog Graph, Plotting OD550 vs Time on a Semilog Graph, Estimating Generation Time from a Semilog Plot of OD550 vs Time, Plotting Cell Concentration versus Time on a Semilog Graph, Determining Generation Time Directly from a Semilog Plot of ... Mostrar Tudo |
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Thesagro: |
Biologia Molecular; Biotecnologia; Matemática. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 07186nam a2200157 a 4500
001 1142776
005 2009-02-17
008 2003 bl uuuu 0 #d
100 1 $aSTEPHENSON, F. H.
245 $aCalculations in molecular biology and biotechnology$ba guide to mathematics in the laboratory.
260 $aAmsterdam: Academic Press$c2003
300 $c1 CD-ROM.
520 $aIntroduction, Significant Digits, Rounding Off Significant Digits in Calculations, Exponents and Scientific Notation, Expressing Numbers in Scientific Notation, Converting Numbers from Scientific Notation to Decimal Notation, Adding and Subtracting Numbers Written in Scientific Notation, Multiplying and Dividing Numbers Written in Scientific Notation, Metric Prefixes, Conversion Factors and Canceling Terms, Section 2: Solutions, Mixtures, and Media Introduction, Calculating Dilutions: A General Approach, Concentrations by a Factor of X, Preparing Percent Solutions, Diluting Percent Solutions, Moles and Molecular Weight: Definitions, Molarity, Diluting Molar Solutions, Converting Molarity to Percent, Converting Percent to Molarity, Normality, PH, pKa and the Henderson-Hasselbalch Equation, Section 3: Cell Growth The Bacterial Growth Curve, Manipulating Cell Concentration, Plotting OD550 versus Time on a Linear Graph, Plotting the Logarithm of OD550 vs Time on a Linear Graph, Logarithms, Sample OD550 Data Converted to Log Values, Plotting Log OD550 versus Time, Plotting the Log of Cell Concentration versus Time, Determining Log Values, Calculating Generation Time, Slope and Growth Constant, Generation Time, Plotting Cell Growth Data on a Semilog Graph, Plotting OD550 vs Time on a Semilog Graph, Estimating Generation Time from a Semilog Plot of OD550 vs Time, Plotting Cell Concentration versus Time on a Semilog Graph, Determining Generation Time Directly from a Semilog Plot of Cell Concentration vs Time, Plotting Cell Density versus OD550 on a Semilog Graph, The Fluctuation Test, Fluctuation Test Example, Variance, Measuring Mutation Rate, The Poisson Distribution, Calculating Mutation Rate by Using Poisson Distribution, Using a Graphical Approach to Calculate Mutation Rate from Fluctuation Test Data, Mutation Rate Determined by Plate Spreading, Measuring Cell Concentration in a Hemocytometer, Section 4: Working with Bacteriophage Introduction, Multiplicity of Infection, Probabilities and moi, Measuring Phage Titer, Diluting Bacteriophage, Measuring Burst Size, Section 5: Quantitation of Nucleic Acids, Quantitation of Nucleic Acids by UV Spectroscopy, Determining the Concentration of Double-Stranded DNA, Using Absorbance and an Extinction Coefficient to Calculate Double-Stranded DNA Concentration, Calculating DNA Concentration as a Millimolar (mM) Amount, Determining the Concentration of Single-Stranded DNA Molecules, Single-Stranded DNA Concentration Expressed in ?g/mL, Determining the Concentration of Large Molecular Weight Single-Stranded DNA, (ssDNA) in pmol/?L, Expressing ssDNA Concentration as a mM Amount, Oligonucleotide Quantitation, OD Units, Expressing an Oligonucleotide's Concentration in ?g/mL, Oligonucleotide Concentration Expressed in pmol/?L, Measuring RNA Concentration, Molecular Weight, Molarity, and Nucleic Acid Length, Estimating DNA Concentration on an Ethidium Bromide Stained Gel, Section 6: Labeling Nucleic Acids with Radioisotopes Introduction, Using Radioactivity - The Curie, Estimating Plasmid Copy Number, Labeling DNA by Nick Translation, Determination of Percent Incorporation of Radioactive Label , Calculating Specific Radioactivity of a Nick Translation Product, Random Primer Labeling of DNA, Random Primer Labeling - Percent Incorporation, Random Primer Labeling - Calculating Theoretical Yield, Random Primer Labeling - Calculating Actual Yield, Random Primer Labeling - Calculating SpecificActivity of the Product, Labeling 3' Termini with Terminal Transferase, 3'-End Labeling with Terminal Transferase -Percent Incorporation, 3'-End Labeling with Terminal Transferase - Specific Activity of the Product, cDNA Synthesis, First Strand cDNA Synthesis, Second Strand cDNA Synthesis, Homopolymeric Tailing, In vitro Transcription, Section 7: Oligonucleotide Synthesis Introduction, Synthesis Yield, Measuring Stepwise and Overall Yield by the DMT Cation Assay, Overall Yield, Stepwise Yield, Calculating Micromoles of Nucleoside Added at Each Base Addition Step, Section 8: The Polymerase Chain Reaction Introduction, Template and Amplification , Exponential Amplification, PCR Efficiency, Calculating the Tm of the Target Sequence, Primers, Primer Tm, Calculating Tm Based on Salt Concentration, G/C Content, and DNA Length, Calculating Tm Based on Nearest Neighbor Interactions, DNTPs, DNA Polymerase, Calculating DNA Polymerase's Error Rate, Quantitative PCR, Section 9: Recombinant DNA Introduction, Restriction Endonucleases, The Frequency of Restriction Endonuclease Cut Sites, Calculating the Amount of Fragment Ends, The Amount of Ends Generated by Multiple Cuts, Ligation, Ligation Using Lambda-Derived Vectors, Packaging of Recombinant Lambda Genomes, Ligation Using Plasmid Vectors, Transformation Efficiency Genomic Libraries: How Many Clones do You Need? , cDNA Libraries: How Many Clones is Enough? , Expression Libraries, Screening Recombinant Libraries by Hybridization to DNA Probes, Oligonucleotide Probes, Hybridization Conditions, Hybridization Using Double-Stranded DNA Probes, Sizing DNA Fragments by Gel Electrophoresis, Generating Nested Deletions Using Nuclease BAL 31, Section 10: Protein Introduction, Protein Quantitation by Measuring Absorbance at 280 nm, Using Absorbance Coefficients and Extinction Coefficients to Estimate Protein, Concentration, Relating Absorbance Coefficient to Molar Extinction Coefficient, Determining a Protein's Extinction Coefficient, Relating mg/mL Concentration to Molarity, Protein Quantitation Using A280 when Contaminating Nucleic Acids are Present, Protein Quantitation at 205 nm, Protein Quantitation at 205 nm when Contaminating Nucleic Acids are Present, Measuring Protein Concentration by Colorimetric Assay - The Bradford Assay, Using b-Galactosidase to Monitor Promoter Activity and Gene Expression, Assaying b-Galactosidase in Cell Culture, Specific Activity, Assaying b-Galactosidase from Purified Extracts, The CAT Assay, Calculating Molecules of CAT, Use of Luciferase in a Reporter Assay, In vitro Translation - Determining Amino Acid Incorporation, Section 11: Centrifugation Introduction, Relative Centrifugal Force (g Force, ) Converting g Force to rpm, Determining g Force and rpm by Use of a Nomogram, Calculating Sedimentation Times, Section 12: Forensic Science Introduction, Alleles and Genotypes, Calculating Genotype Frequencies, Calculating Allele Frequencies, The Hardy-Weinberg Equation and Calculating Expected Genotype Frequencies, The Chi-square Test: Comparing Observed to Expected Values, Sample Variance, Sample Standard Deviation, Pi: The Power of Inclusion, Pd: The Power of Discrimination, DNA Typing and a Weighted Average, The Multiplication Rule, Index
650 $aBiologia Molecular
650 $aBiotecnologia
650 $aMatemática
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Embrapa Semiárido (CPATSA) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Florestas. Para informações adicionais entre em contato com cnpf.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Florestas. |
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Data corrente: |
25/08/2017 |
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Data da última atualização: |
25/08/2017 |
|
Tipo da produção científica: |
Orientação de Tese de Pós-Graduação |
|
Autoria: |
CADEMARTORI, P. H. G. de. |
|
Título: |
Modificação da superfície de madeira e de produtos à base de madeira por plasma frio. |
|
Ano de publicação: |
2017 |
|
Fonte/Imprenta: |
2017. |
|
Páginas: |
139 f. |
|
Idioma: |
Português |
|
Notas: |
Tese (Doutorado em Engenharia Florestal) - Setor de Ciências Agrárias, Universidade Federal do Paraná, Curitiba. Orientadora: Graciela Ines Bolzon de Muniz; Coorientadores: Washington Luiz Esteves Magalhães, Silvana Nisgoski. |
|
Palavras-Chave: |
Adesão interfacial; Energia de superfície; Hidrofobicidade; Interfacial adhesion; Modificação de superfície; Plasma de baixa temperatura; Plasma technology; Surface energy; Surface modification; Tecnologia de plasma. |
|
Thesagro: |
Painel de madeira. |
|
Thesaurus NAL: |
Hydrophobicity; Wettability. |
|
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
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Marc: |
LEADER 01031nam a2200277 a 4500
001 2074491
005 2017-08-25
008 2017 bl uuuu m 00u1 u #d
100 1 $aCADEMARTORI, P. H. G. de
245 $aModificação da superfície de madeira e de produtos à base de madeira por plasma frio.
260 $a2017.$c2017
300 $a139 f.
500 $aTese (Doutorado em Engenharia Florestal) - Setor de Ciências Agrárias, Universidade Federal do Paraná, Curitiba. Orientadora: Graciela Ines Bolzon de Muniz; Coorientadores: Washington Luiz Esteves Magalhães, Silvana Nisgoski.
650 $aHydrophobicity
650 $aWettability
650 $aPainel de madeira
653 $aAdesão interfacial
653 $aEnergia de superfície
653 $aHidrofobicidade
653 $aInterfacial adhesion
653 $aModificação de superfície
653 $aPlasma de baixa temperatura
653 $aPlasma technology
653 $aSurface energy
653 $aSurface modification
653 $aTecnologia de plasma
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