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DNA Extraction from Bacteria
DNA Extraction from Bacteria

... Step 3. Remove the tube from the hot water bath. Add cold alcohol to the test tube (about 2/3 full) to create an alcohol layer on top of the bacterial solution. Do this by slowly pouring the alcohol down the inside of the test tube with a Pasteur pipette or medicine dropper. DO NOT MIX! DNA is solu ...
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... – DNA sequences that serve as attachments sites for the DNAbinding proteins that regulate the initiation of transcription. ...
Chapter 13 Genetic Engineering - Mrs. Moyer
Chapter 13 Genetic Engineering - Mrs. Moyer

... can synthesize a DNA strand and connect it to a circular DNA molecule known as a plasmid… which can be found naturally in bacteria. This bacteria can then be injected into a plant, and will insert its DNA into the plant. ► If transformation is successful, the recombinant DNA is integrated into one o ...
Question How does DNA control a cell?By controlling Protein
Question How does DNA control a cell?By controlling Protein

... in changes in phenotype (17.5). ...
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... Prior modification experiments identify all those sites that the enzyme must recognize in order to bind. Protection experiments recognize all those sites that actually make contact in the binary complex The regions at –35 and –10 contain most of the contact points for the enzyme. Within these region ...
12.3 DNA, RNA, and Protein Molecular Genetics
12.3 DNA, RNA, and Protein Molecular Genetics

... The Genetic Code: • Because there are four different bases, there are 64 possible three-base codons (4 × 4 × 4 = 64). • Some amino acids can be specified by more than one codon. • For example, six different codons specify the amino acid leucine, and six others specify arginine. ...
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Nessun titolo diapositiva

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The Good, the bad and the ugly of Genetic Engineering
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HISTOCHEMISTRY : Feulgen Technique for DNA

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... loci a variable number of times. Both the sequence and the copy-number of these repeats vary from individual to individual. These are the polymorphisms targeted by DNA fingerprinting. E.g. there is a region of DNA just beyond the insulin gene on chromosome 11, consisting of 7 to 40 repeats, dependin ...
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... from cell division will each have a complete copy of the DNA necessary for the cell to survive. As we will see, DNA replication utilizes several different types of enzymes to link free nucleotides together into new strands of DNA. Slide 3 During DNA replication, DNA is unwound from its double helix, ...
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DNA Timeline - WordPress.com
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Chapter 11: DNA and Genes
Chapter 11: DNA and Genes

... • Some codons do not code for amino acids; they provide instructions for making the protein. • More than one codon can code for the same amino acid. • However, for any one codon, there can be only one amino acid. • All organisms use the same genetic code. • This provides evidence that all life on E ...
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tggccatcgtaaggtgcgacc ggtagca

... Name: _____________________ DNA vs. Genes vs. Chromosomes Definitions 1. DNA is a nucleic acid that contains the sequence for all our traits. 2. Genes are sections of DNA that code for a particular trait. 3. Chromosomes are condensed DNA fibers, each containing several genes ...
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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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