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...  Make covalent bonds between nucleotides of the new strands  Fast, accurate process  Error only one in a billion nucleotides ...
Chapter 24: Promoters and Enhancers
Chapter 24: Promoters and Enhancers

... with a target promoter. • The principle is that an enhancer works in any situation in which it is constrained to be in proximity with the promoter. • Enhancers Work by Increasing the Concentration of Activators Near the Promoter ...
Chapter 25
Chapter 25

... • RNAPI promoters: - are species specific, each RNAPI recognizes a specific promoter. - are located -186 to +6 on the DNA template strand. • RNAPII promoters: - The constitutive genes have GC box (GGGCGG consensus sequence) in their promoters - The structural genes have TATA box (TATATAATA sequence) ...
Nucleotides and Nuclic Acids
Nucleotides and Nuclic Acids

... In eukaryotes, formation of nucleosomes results in torsional strain in the DNA molecule (equivalent to ~1.5-1.8 supercoils/nucleosome particle theoretically; actual value is ~1), which is relieved by topoisomerases. This results in DNA that is negatively supercoiled once histone proteins are removed ...
Human Genome
Human Genome

... 7. Alu analysis: there may be strong selection in favor of preferential retention of Alu elements in the GC rich regions and that these ‘selfish’ elements may benefit their human hosts 8. The mutation rate is about twice as high in maleas in female meiosis. Thus, most mutation occurs in males 9. Lar ...
PDQeX Standard - DNA Extraction
PDQeX Standard - DNA Extraction

... quantitative, multiplex and routine PCR applications. ...
Taxonomic distribution of Large DNA viruses in the sea
Taxonomic distribution of Large DNA viruses in the sea

...  The GOS data comprise a large environmental shotgun sequence collection, with 7.7 million sequencing reads assembled into 4.9 billion bp contigs  At least 3% of the predicted proteins contained within the GOS data are of viral origin  Most DNA samples were extracted from the 0.1-0.8 μsized fract ...
aptamers04
aptamers04

... Most have to do with nucleic acid transformations; RNase, ligase, kinase, etc. But not all (C-C bond formation). Generally much slower than protein enzymes. Most work has been on RNases (usually associated with the word “ribozymes”) ...
000 EXAM 2 study guide
000 EXAM 2 study guide

... 3. Understand what it means to say the genetic code is degenerate, unambiguous, nonoverlapping, and has relaxed base-pairing rules at the 3rd base due to wobble. 4. Know start and stop codons from the genetic code. Does a stop codon code for an amino acid? If you had a sequence of 30 nucleotides tha ...
CHNOPS Lab
CHNOPS Lab

Section 8.4: Transcription
Section 8.4: Transcription

CHAPTER 14 LECTURE NOTES: RECOMBINANT DNA
CHAPTER 14 LECTURE NOTES: RECOMBINANT DNA

struktur dan fungsi kromosom
struktur dan fungsi kromosom

... arises from DNAs association with histones ...
Genetic Engineering
Genetic Engineering

... transcriptase can be used to obtain coding regions without introns. ...
Chapter 1 Genes Are DNA
Chapter 1 Genes Are DNA

... • Nucleases are enzymes that degrade nucleic acids; they include DNases and RNases and can be categorized as endonucleases or exonucleases. ...
Document
Document

Section J Analysis and Uses of Cloned DNA
Section J Analysis and Uses of Cloned DNA

RNA
RNA

... intron or exon-exon junction spanning length: 9-30 bp (ideally: 20 bp) melting temperature Tm: 58-60 °C (ideally: 59°C) ...
Slide 1
Slide 1

... – If chromosome is lost (one copy = monosomic) = individual does not survive – If chromosome is gained (3 copies = trisomic) = individual may survive but only in a few cases and will be mentally impaired • Example: Trisopy 21 (Down syndrome) ...
for DNA and RNA
for DNA and RNA

... A key consideration for Personalis Cancer Analysis is to submit specimens that contain the amount of DNA and/or RNA necessary for sequencing and analysis. The following information is being included as a guideline. ...
The Art and Science of PCR
The Art and Science of PCR

... thousands of bases (if you did a nice job with your extraction). Notice that the 5’ and 3’ ends of the ...
Ch. 14 - Crestwood Local Schools
Ch. 14 - Crestwood Local Schools

... bases) that are made on the lagging strand. All Okazaki fragments must be primed. RNA primer is removed after DNA is added. ...
Chapter-9-Chromosomes-and-DNA-Replication
Chapter-9-Chromosomes-and-DNA-Replication

... The new DNA is built up from the four nucleotides (A, C, G and T) that are abundant (free nucleotides) in the nucleoplasm. These nucleotides attach themselves to the bases on the old strands by complementary base pairing. Where there is a T base, only an A nucleotide will bind, and so on. DNA polyme ...
Chapter 36: RNA Synthesis and Regulation in Bacteria.
Chapter 36: RNA Synthesis and Regulation in Bacteria.

... Chapter 36: RNA Synthesis and Regulation in Bacteria. 1. Define the three main types of RNA. 2. What are the nucleotides that are used to synthesize RNA? 3. What is the direction of RNA polymerization? 4. What is meant by the statement “RNA polymerization is thermodynamically assisted by PPi hydroly ...
The role of DNA damage in laminopathy progeroid syndromes
The role of DNA damage in laminopathy progeroid syndromes

... promotes nuclear shape abnormalities and cellular toxicity [2–5]. The initial post-translational processing of lamin A is now well-characterized. Lamin A is first translated as a precursor molecule termed prelamin A that possesses a Cterminal motif, CaaX (where a is an aliphatic residue), which is a ...
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Bisulfite sequencing



Bisulphite sequencing (also known as bisulfite sequencing) is the use of bisulphite treatment of DNA to determine its pattern of methylation. DNA methylation was the first discovered epigenetic mark, and remains the most studied. In animals it predominantly involves the addition of a methyl group to the carbon-5 position of cytosine residues of the dinucleotide CpG, and is implicated in repression of transcriptional activity.Treatment of DNA with bisulphite converts cytosine residues to uracil, but leaves 5-methylcytosine residues unaffected. Thus, bisulphite treatment introduces specific changes in the DNA sequence that depend on the methylation status of individual cytosine residues, yielding single- nucleotide resolution information about the methylation status of a segment of DNA. Various analyses can be performed on the altered sequence to retrieve this information. The objective of this analysis is therefore reduced to differentiating between single nucleotide polymorphisms (cytosines and thymidine) resulting from bisulphite conversion (Figure 1).
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