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2.3 Carbon-Based Molecules
2.3 Carbon-Based Molecules

2.3 Carbon-Based Molecules
2.3 Carbon-Based Molecules

Isolation and Characterization of Two Polypeptides
Isolation and Characterization of Two Polypeptides

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. ...
2.3 Carbon-Based Molecules KEY CONCEPT Carbon-based molecules are the foundation of life.
2.3 Carbon-Based Molecules KEY CONCEPT Carbon-based molecules are the foundation of life.

2.3 Carbon-Based Molecules
2.3 Carbon-Based Molecules

13-2 Manipulating DNA
13-2 Manipulating DNA

... Copyright Pearson Prentice Hall ...
Types of RNA: mRNA, rRNA and tRNA - Progetto e
Types of RNA: mRNA, rRNA and tRNA - Progetto e

A simple and improved PCR-based technique for white
A simple and improved PCR-based technique for white

... cross-species application of similar zinc-finger based techniques (Morin et al. 2005; Shaw et al. 2003; Wilson and White 1998). Although previous studies have provided more complicated protocols to distinguish sexes of whitetailed deer tissue samples, this technique provides several advantages for r ...
CHMI 2227E Biochemistry I
CHMI 2227E Biochemistry I

Data Supplement
Data Supplement

Document
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7.2 Nucleic acids
7.2 Nucleic acids

Fig. 1.12
Fig. 1.12

... Palindromic and self-complementary sequences. It has no simple, regular secondary structure that serves as a ...
2 - chrisbonline.com
2 - chrisbonline.com

intact-protein based sample preparation strategies for
intact-protein based sample preparation strategies for

... consist of three major types: (1) tissues, (2) cell populations, and (3) biological fluids. A common feature of biological samples is their extraordinary complexity because of the high multidimensionality of their protein constituents, which differ in their cellular and subcellular distribution; the ...
Complete Protocol
Complete Protocol

... The appropriate incubation temperature will vary from one translation system to another. Please refer to the appropriate Promega protocol for specific reaction conditions. ...
QPCR Helpful Hints
QPCR Helpful Hints

RNA and DNA and protein PLUS mciro info sheet2.pub
RNA and DNA and protein PLUS mciro info sheet2.pub

... rapid method for the isolation and purification of total RNA, genomic DNA and proteins sequentially from a single sample of cultured animal cells, small tissue samples, microdissected samples including laser-capture microdissection (LCM), blood, fungi or plants. The total RNA, genomic DNA and protei ...
pGLO Transformation and Purification of Green
pGLO Transformation and Purification of Green

pGLO Transformation and Green Fluorescent Protein - Bio-Rad
pGLO Transformation and Green Fluorescent Protein - Bio-Rad

An endosperm enzyme catalyzes the formation of phosphotriester
An endosperm enzyme catalyzes the formation of phosphotriester

... this high molecular structure of nucleic acid complex, although the detail of structures is not known at the present time, in maize endosperms and Arabiadopsis leaves. A simple overall enzyme reaction mechanism can be depicted as follows: Nucleotides + Enzyme <-------------> Enzyme-Nucleotide(s) com ...
an integrated microsystem for allele
an integrated microsystem for allele

... The microsystem has a second PCR chamber (PCR2) for performing an allele-specific amplification. By design of the allele-specific primers, PCR amplification only occurs if a SNP is present [7]. To further illustrate the operational concept, allele-specific PCR is conducted in a commercially availab ...
RNA and Protein Synthesis
RNA and Protein Synthesis

Pierce Trypsin Protease, MS Grade
Pierce Trypsin Protease, MS Grade

< 1 ... 13 14 15 16 17 18 19 20 21 ... 69 >

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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