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Lab Investigation: Examining a Single Gene
Lab Investigation: Examining a Single Gene

... You will load both your PCR reactions and standard DNA markers sample into the gel. A standard DNA marker has a bunch of different sized pieces of DNA so you can compare it to the DNA from your PCR reaction to figure out what size piece it is. Two or three groups can share a gel, but only one molecu ...
The Genetic Code
The Genetic Code

... the right side of the chart • it must be in the same row as the first letter ...
Image PowerPoint
Image PowerPoint

... spark. Condensers cooled any gases, causing molecular products to collect in the water. From this water, samples were taken over the next week and analyzed. Among the organic molecules formed were amino acids, basic building blocks of protein. Subsequent follow-up trials, by many other biologists, u ...
The beauty of science - University of California, Irvine
The beauty of science - University of California, Irvine

... Visualizing DNA Genes/regions of interest in larger pieces of DNA Isolate gene/region of interest to study it/products Examples of things you can do with DNA: ...
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Chromosomes come in pairs

... sequence, or any other alteration of the genome that is not manifested as reciprocal recombination. ...
Year 10 Term 2: Evolution Weeks 6-10
Year 10 Term 2: Evolution Weeks 6-10

... development of the scientific theory of evolution Activity 2.1.1: Analysing beaks Oxford pg 62 Describe how the theory of plate tectonics can help explain the biogeography of the world Compare artificial and natural selection using examples. Activity 2.1.2: Sexual selection in humans Oxford pg 65 Ch ...
TruSeq™ Sample Preparation Best Practices and Troubleshooting
TruSeq™ Sample Preparation Best Practices and Troubleshooting

... diluting concentrated libraries for making clusters. ` Small differences in volumes (±0.5 μl) can sometimes give rise to very large  differences in cluster numbers (~100,000). ` Small volume pipetting can be a source of potential error in protocols that require  generation of standard curves, such a ...
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Chapter 8: Cell Division
Chapter 8: Cell Division

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Changes in Prokaryotic Transcription: Phage Lambda and Others
Changes in Prokaryotic Transcription: Phage Lambda and Others

... now continues through, producing a polycistronic mRNA. The same thing happens for transcription from the rightward promoter, PR. As a result, a number of gene products are made, not just N and cro. One of these is Q, another antiterminator that eventually opens up full transcription of all the late ...
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... • DNA wraps around proteins and compacts (made smaller) to be made into chromosomes. • Genes are on chromosomes • A gene is a segment of DNA at a specific location on a chromosome that influences heredity characteristic. ...
Section E
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... • Both leading and lagging strand primers are elongated by DNA polymerase III holoenzyme. This complex is a dimer, – One half synthesizes the leading strand; – The other synthesizes the lagging strand; – The two polymerases in a single complex ensures that both strands are synthesized at the same ra ...
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... 1. Eventually a stop codon is reached on the mRNA This final codon on mRNA contains termination signal 2. Releasing factors cleave polypeptide chain from tRNA that carried final amino acid. The newly synthesised polypeptide leaves the ribosome. 3. mRNA is released from ribosome and broken down into ...
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... 37. In maize, two plants that are heterozygous for the recessive alleles a and b are crossed, what frequency of double-mutant progeny will appear if a and b are 7.2 map units apart, and both parents carry a and b in trans (configuration)? a. 0.036; b. 0.0625; c. 0.001296 d. 0.005184; e. 0.072. 38. I ...
Genetic Variation & Evolution
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heredity The passing of traits from parents to offspring. fertilization

... The passing of traits from parents to offspring. ...
book ppt - Castle High School
book ppt - Castle High School

... Mutations can also be defined in terms of their effects on polypeptide sequences. Silent mutations have no effect on amino acids—often found in noncoding regions of DNA. A base substitution does not always affect amino acid sequence, which may be repaired in translation. ...
Chapter 10 DNA to Protein
Chapter 10 DNA to Protein

... Mutations can also be defined in terms of their effects on polypeptide sequences. Silent mutations have no effect on amino acids—often found in noncoding regions of DNA. A base substitution does not always affect amino acid sequence, which may be repaired in translation. ...
DISCOVERING DNA Biology Practical—DNA extraction
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Chapter 13 Mutation, DNA Repair, and Recombination
Chapter 13 Mutation, DNA Repair, and Recombination

... Induced mutations occur upon exposure to physical or chemical mutagens.  Hermann J. Muller and Edgar Alternburg measured the frequency of X-linked recessive lethal mutations in Drosophila.  Muller demonstrated that exposing Drosophila sperm to X-rays increased the mutation frequency. ...
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Class Notes
Class Notes

... The bridge between DNA and protein synthesis is the nucleic acid RNA. ...
CHAPTER 17 FROM GENE TO PROTEIN
CHAPTER 17 FROM GENE TO PROTEIN

... The bridge between DNA and protein synthesis is the nucleic acid RNA. ...
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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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