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Properties of Enzymes
Properties of Enzymes

... Properties of Enzymes ...
CpG methylation analysis from targeted
CpG methylation analysis from targeted

... Targeted bisulfite sequencing data provides a unique set of challenges. The majority of bisulfite-treated DNA is devoid of cytosines, which creates difficulties when mapping the short sequencing reads from Next-Generation Sequencing platforms. Due to the nature of a bisulfite converted genome, the s ...
Altering protein specificity: techniques and applications
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Chapter 8 The Cellular Basis of Reproduction and Inheritance
Chapter 8 The Cellular Basis of Reproduction and Inheritance

Supplementary Information (doc 38K)
Supplementary Information (doc 38K)

... were used against BCL2 (05N51-20), BCL6 (01N23-020) and C-MYC (01N63- ...
Myriad - Tech Transfer Central
Myriad - Tech Transfer Central

... is representative of this class of claims: A method for diagnosing a predisposition for breast cancer in a human subject which comprises comparing the germline sequence of the BRCA2 gene or the sequence of its mRNA in a tissue sample from said subject with the germline sequence of the wild-type BRCA ...
Chapter 13 Genetics and Biotechnology
Chapter 13 Genetics and Biotechnology

... requires heat, the DNA polymerase used in PCR has to be able to withstand high temperatures. This special DNA polymerase was isolated from a thermo–philic, or heat-loving, bacterium such as those found living in ...
Breaking PCR - Integrated DNA Technologies
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Recombination, Bacteriophages, and Horizontal Gene Transfer
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... • The F factor can exist in three different states: • F+ refers to a factor in an autonomous, extrachromosomal state containing only the genetic information described above. • The "Hfr" (which refers to "high frequency recombination") state describes the situation when the factor has integrated itse ...
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Edexcel GCE - The Student Room
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Isolating, Cloning, and Sequencing DNA
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... to separate these by size, the much more porous gels formed by dilute solutions of agarose (a polysaccharide isolated from seaweed) are used (Figure 8-23B). These DNA separation methods are widely used for both analytical and preparative purposes. Figure 8-23. Gel electrophoresis techniques for sepa ...
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Chapter 8 Enzymes: Basic Concepts and Kinetics
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Analytical and Chromatography - Sigma

... syndromes: Werner and Bloom Syndromes. MRE11 complex is mutated in genetic instability syndromes: Nijmegen breakage syndrome and ataxia telangiectasia-like disorder. All three may be involved in the resolution of a stalled replication fork and in checkpoint signaling during S phase. DNA replication ...
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Deoxyribozyme



Deoxyribozymes, also called DNA enzymes, DNAzymes, or catalytic DNA, are DNA oligonucleotides that are capable of catalyzing specific chemical reactions, similar to the action of other biological enzymes, such as proteins or ribozymes (enzymes composed of RNA).However, in contrast to the abundance of protein enzymes in biological systems and the discovery of biological ribozymes in the 1980s,there are no known naturally occurring deoxyribozymes.Deoxyribozymes should not be confused with DNA aptamers which are oligonucleotides that selectively bind a target ligand, but do not catalyze a subsequent chemical reaction.With the exception of ribozymes, nucleic acid molecules within cells primarily serve as storage of genetic information due to its ability to form complementary base pairs, which allows for high-fidelity copying and transfer of genetic information. In contrast, nucleic acid molecules are more limited in their catalytic ability, in comparison to protein enzymes, to just three types of interactions: hydrogen bonding, pi stacking, and metal-ion coordination. This is due to the limited number of functional groups of the nucleic acid monomers: while proteins are built from up to twenty different amino acids with various functional groups, nucleic acids are built from just four chemically similar nucleobases. In addition, DNA lacks the 2'-hydroxyl group found in RNA which limits the catalytic competency of deoxyribozymes even in comparison to ribozymes.In addition to the inherent inferiority of DNA catalytic activity, the apparent lack of naturally occurring deoxyribozymes may also be due to the primarily double-stranded conformation of DNA in biological systems which would limit its physical flexibility and ability to form tertiary structures, and so would drastically limit the ability of double-stranded DNA to act as a catalyst; though there are a few known instances of biological single-stranded DNA such as multicopy single-stranded DNA (msDNA), certain viral genomes, and the replication fork formed during DNA replication. Further structural differences between DNA and RNA may also play a role in the lack of biological deoxyribozymes, such as the additional methyl group of the DNA base thymidine compared to the RNA base uracil or the tendency of DNA to adopt the B-form helix while RNA tends to adopt the A-form helix. However, it has also been shown that DNA can form structures that RNA cannot, which suggests that, though there are differences in structures that each can form, neither is inherently more or less catalytic due to their possible structural motifs.
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