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Biochemistry I, Spring Term 2004 - Second Exam:
Biochemistry I, Spring Term 2004 - Second Exam:

Supporting Information Heim et al. 10.1073/pnas.1413018111
Supporting Information Heim et al. 10.1073/pnas.1413018111

simultaneous detection of four food borne bacterial pathogens by
simultaneous detection of four food borne bacterial pathogens by

Biochemistry I, Spring Term 2004 - Second Exam:
Biochemistry I, Spring Term 2004 - Second Exam:

Chapter 3 - McGraw Hill Higher Education
Chapter 3 - McGraw Hill Higher Education

Product Manual Plant DNA Isolation Reagent
Product Manual Plant DNA Isolation Reagent

Transcription
Transcription

`RNA world`.
`RNA world`.

... It has ceded primacy as the repository of genetic information to DNA but it has gained versatility. It is a master architect, forming complex, threedimensional structures, and it can carry out catalysis, a trick it learned long before proteins knew how to be enzymes. In short, life probably evolved ...
Lesson title: Nucleic acids Lesson date: 30.12.2013 One sentence
Lesson title: Nucleic acids Lesson date: 30.12.2013 One sentence



Towards an Analysis of the Rice Mitochondrial Proteome
Towards an Analysis of the Rice Mitochondrial Proteome

2.3 Carbon-Based Molecules
2.3 Carbon-Based Molecules

... • Proteins are polymers of amino acid monomers. – Twenty different amino acids are used to build proteins in organisms. – Amino acids differ in side groups, or R groups. – Amino acids are linked by peptide bonds. ...
Novel Amycolatopsis balhimycina biochemical abilities
Novel Amycolatopsis balhimycina biochemical abilities

... extraction buffer, respectively. All samples were loaded on 12% SDS-PAGE for protein separation (data not shown). Eighteen polyacrylamide gel slices per sample were generated and subjected to tryptic digestion for tandem MS procedures. Although not quantitative, this approach allowed to recognize mo ...
Protein-Protein Interactions
Protein-Protein Interactions

Brief Introduction of Single Nucleotide Polymorphism: Basic Concept
Brief Introduction of Single Nucleotide Polymorphism: Basic Concept

... (adapted from: “Single Nucleotide Polymorphism–methods and protocols”. 2009. ed. by A. A. Komar , Humana Press ) 1. SNPs: Impact on Gene Function and Phenotype Single nucleotide polymorphism (SNP) is the simplest form of DNA variation among individuals. These simple changes can be of transition or t ...
Document
Document

HEMOGLOBINOPATHY412 KB
HEMOGLOBINOPATHY412 KB

RNA - Southgate Schools
RNA - Southgate Schools

Proteolysis in Mixed Organic-Aqueous Solvent
Proteolysis in Mixed Organic-Aqueous Solvent

Assessment of Genomic DNA Quality by Microchip Electrophoresis
Assessment of Genomic DNA Quality by Microchip Electrophoresis

... availability of high-quality genomic DNA (gDNA) and a reliable method to assess this quality are essential. For techniques such as next-generation sequencing (NGS) and molecular diagnostics, ensuring that gDNA is intact (having a high size distribution and being free of degradation) is critical to o ...
A Toc75-like protein import channel is abundant in chloroplasts
A Toc75-like protein import channel is abundant in chloroplasts

A Toc75like protein import channel is abundant in
A Toc75like protein import channel is abundant in

2.3 Carbon-Based Molecules
2.3 Carbon-Based Molecules

Chapter 5
Chapter 5

... 10. A gene is inserted into an ampicillin resistance gene in a plasmid. Will cells containing the resulting recombinant plasmid be sensitive or resistant to ampicillin? Answer: When inserted into a gene, the new DNA interrupts the previous gene. Thus, the antibiotic gene is unlikely to be functional ...
2.3 Carbon-Based Molecules
2.3 Carbon-Based Molecules

... • Proteins are polymers of amino acid monomers. – Twenty different amino acids are used to build proteins in organisms. – Amino acids differ in side groups, or R groups. – Amino acids are linked by peptide bonds. ...
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Gel electrophoresis



Gel electrophoresis is a method for separation and analysis of macromolecules (DNA, RNA and proteins) and their fragments, based on their size and charge. It is used in clinical chemistry to separate proteins by charge and/or size (IEF agarose, essentially size independent) and in biochemistry and molecular biology to separate a mixed population of DNA and RNA fragments by length, to estimate the size of DNA and RNA fragments or to separate proteins by charge.Nucleic acid molecules are separated by applying an electric field to move the negatively charged molecules through a matrix of agarose or other substances. Shorter molecules move faster and migrate farther than longer ones because shorter molecules migrate more easily through the pores of the gel. This phenomenon is called sieving.Proteins are separated by charge in agarose because the pores of the gel are too large to sieve proteins. Gel electrophoresis can also be used for separation of nanoparticles.Gel electrophoresis uses a gel as an anticonvective medium and/or sieving medium during electrophoresis, the movement of a charged particle in an electrical field. Gels suppress the thermal convection caused by application of the electric field, and can also act as a sieving medium, retarding the passage of molecules; gels can also simply serve to maintain the finished separation, so that a post electrophoresis stain can be applied. DNA Gel electrophoresis is usually performed for analytical purposes, often after amplification of DNA via PCR, but may be used as a preparative technique prior to use of other methods such as mass spectrometry, RFLP, PCR, cloning, DNA sequencing, or Southern blotting for further characterization.
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