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Regulation of Bacterial Conjugation in Microaerobiosis by
Regulation of Bacterial Conjugation in Microaerobiosis by

... screw-capped tube. One hundred microliters of a bacterial suspension (108 bacterial cells) was then added. The treatment was allowed to proceed at 37° during 30 min, without shaking. Two hundred microliters of DES-treated bacterial suspension was then used to start a liquid culture in LB medium. Wh ...
Direct Deletion Analysis in Two Duchenne Muscular Dystrophy
Direct Deletion Analysis in Two Duchenne Muscular Dystrophy

... We determined the segregation of the STR (CA)n alleles that were located within the deletion-prone regions 5’DYS-II, 07A, 5’-7n4, STR 44, STR 45, STR 49, and STR 50. The PCR products of the alleles were analyzed by superimposing the traces of the proband to that of her relatives. The haplotypes of t ...
Mutations in FUS, an RNA Processing Protein, Cause Familial
Mutations in FUS, an RNA Processing Protein, Cause Familial

... or H517Q FUS/TLS–GFP fusion proteins. Immunoblotting of fractions followed by immunostaining with an antibody to GFP demonstrated a substantially higher ratio of soluble cytosolic to soluble nuclear FUS/TLS for both mutants (Fig. 3B). Additionally, a higher ratio of total insoluble to soluble nuclea ...
Eurofins Legionella PCR (Polymerase Chain Reaction) Technical
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... PCR is a molecular biology technique in which the DNA of micro-organisms is extracted and then amplified (multiple copies are made). This enables the laboratory to determine the presence and quantity of that organism’s DNA in a water sample. As it is the DNA that is being assessed, the technique can ...
A natural chimeric yeast containing genetic material from three species
A natural chimeric yeast containing genetic material from three species

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Aberrant DNA methylation in cancer: potential clinical
Aberrant DNA methylation in cancer: potential clinical

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Supp Mat - Columbia University
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Methods for pattern discovery in unaligned biological sequences
Methods for pattern discovery in unaligned biological sequences

... to build a model for the source generating the pattern. Then, for each input sequence, the substring that best ®ts the model is considered the occurrence of the corresponding pattern. Further details on how models are represented and evaluated will be shown in the section on `Measures of signi®cance ...
IBC Form - Icahn School of Medicine
IBC Form - Icahn School of Medicine

... biological agents, biological toxins and /or Genetically Modified microorganisms to the Biological Safety Officer and to report recombinant DNA and synthetic recombinant DNA activities covered under the NIH Guidelines to the Icahn School of Medicine Institutional Biosafety Committee (ISMMS). Check o ...
RNA Editing, ADAR1, and the Innate Immune Response
RNA Editing, ADAR1, and the Innate Immune Response

... impacts the biogenesis or shifts the targets of the corresponding miRNAs [25,26]. The mechanism and function of RNA editing in these traditional editing sites have been very well summarized in previous reviews [12,16,19,20,27,28]. To date, millions of editing sites have been identified or predicted ...
Commonly Used STR Markers
Commonly Used STR Markers

... • Ability to resolve all alleles clearly: – Easier to resolve 4 base pair difference – Rather than 3, 3 better than 2, etc ...
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Paper - Revision Science
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A hypothesis on the possible contribution of free hypoxanthine and

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ap sample5lab2 - Biology Junction
ap sample5lab2 - Biology Junction

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3D Models Enzyme Student Handout
3D Models Enzyme Student Handout

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tRNA aminoacylation by arginyltRNA synthetase: induced

... active complex formed by a class Ia aminoacyl-tRNA synthetase and its natural cognate tRNA illustrates additional strategies used for speci®c tRNA selection. The enzyme speci®cally recognizes the D-loop and the anticodon of the tRNA, and the mutually induced ®t produces a conformation of the anticod ...
Homologous Recombination Between Episomal Plasmids and Chromosomes in Yeast.
Homologous Recombination Between Episomal Plasmids and Chromosomes in Yeast.

... frequency of reversion consisted of strains that carried the same mutation on the plasmid and the chromosome (“homoallelic transformants”) as well as strains that had never been transformed. Two kinds of reversion are possible because both the ura3- alleles used are amber mutations; therefore, the s ...
The rotary mechanism of the ATP synthase Archives - iGRAD
The rotary mechanism of the ATP synthase Archives - iGRAD

... and the F1 d subunit. At least on a gross level, we finally understood the role of each subunit in the complex. Because of the large size, multiple subunits many of which are integral membrane proteins, and asymmetry, determination of the subunit stoichiometry and defining subunit interactions has bee ...
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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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