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A reliable and efficient method for deleting
A reliable and efficient method for deleting

... gene (Lox511–CAM–Lox511, pCAMLOX) which first affords selection for homologous recombinants, and can then be deleted using Cre-recombinase (Fig. 1B). The floxed CAM gene was ligated between homology A and homology B, to generate pCLPS, the final targeting construct (Fig. 1C). pCLPS was cut with NotI ...
Physical Chemistry, Short talk PC-013 Protein
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... Laboratorium für Physikalische Chemie, ETH Zürich, Switzerland, 2Laboratorium für Anorganische Chemie, ETH Zürich, Switzerland, 3IBCP BMSSI, Lyon, France ...
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In vitro translation with non
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Structure-Function Analysis of the UDP-N-acetyl-D
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AP BIOLOGY Chapter 4 - Livonia Public Schools
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ERN3120 Part 1 March 25 2011 09:00-13:00
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... length of an oligonucleotide can be estimated by CE using known size standards. For example, the size standard used by IDT is a purified 40-mer that is used to define a retention time for the capillary. For example, if the 40-mer standard has a retention time of 22 minutes and the average time betwe ...
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Scenario 3 - People.vcu.edu
Scenario 3 - People.vcu.edu

... Pfam found a motif consistent with the annotation with a good expectation value. Curiously, the motif extends beyond the start of the gene. Mouse away from the bar.* *In real life, information will go away when you mouse away from an informative position. In this simulation you’ll also need to click ...
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Alternative Splicing: How to Get More than One Protein from a Gene
Alternative Splicing: How to Get More than One Protein from a Gene

... Description: Use the word key from the “Protein Synthesis and Words” activity to demonstrate how eukaryotic cells may use one DNA sequence to code for multiple proteins. Eukaryotic cells might use the same gene or DNA sequence differently depending on where the gene is located. A brain cell might ma ...
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BIOLOGY SUPPORT MATERIAL

... Ans: Specialized cells in diploid organism, i.e., gamete mother cell which undergo meiosis. 2- Name the kind of reproduction in bees by which drones are produced? Ans: Parthenogenesis. 3- What is special in flowering bamboo? Ans: Bamboo species flower only once in their life-times generally after 50 ...
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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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