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12.3 RNA and Protein Synthesis
12.3 RNA and Protein Synthesis

... • Messenger RNA (mRNA) carries copies of messages encoded on DNA to the rest of the cell. • Ribosomal RNA (rRNA) makes up part of the ribosome ...
PPT: Genetics: From Mendel to Genome and Epigenome
PPT: Genetics: From Mendel to Genome and Epigenome

... influences on developmental events can affect the phenotype of the adult. The Greek prefix “epi” means “on top of” or “over”, so the term “Epigenetics” literally describes regulation at a level above, or in addition to, those of genetic mechanisms. Robin Holliday and John Pugh proposed that changes ...
isolation and sequencing of a genomic dna encoding for ascorbat
isolation and sequencing of a genomic dna encoding for ascorbat

... I and Bam HI and the combinations among these restriction enzymes. The utilization of these enzymes was imposed by the fact that Sal I sets free the genomic DNA from λ-EMBL-3 phage while the other enzymes do not cut the phage but only the free genomic DNA. The digested DNA was run on a 1% TAE gelaga ...
bio-of-cells-lent-essay-1 310 kb bio-of-cells-lent-essay
bio-of-cells-lent-essay-1 310 kb bio-of-cells-lent-essay

How to obtain a clone of a specific gene
How to obtain a clone of a specific gene

DNA / RNA blue print of life PPT
DNA / RNA blue print of life PPT

... Why not send the original DNA code out? DNA might be damaged! mRNA components are reused To copy more messages ...
DNA, RNA, and Protein Synthesis
DNA, RNA, and Protein Synthesis

... • Each strand of the DNA double helix has all the information needed to reconstruct the other half by the mechanism of base pairing. • In most prokaryotes, DNA replication begins at a single point and continues in two directions • In eukaryotic chromosomes, DNA replication occurs at hundreds of plac ...
Uracil-DNA Glycosylase (UDG)
Uracil-DNA Glycosylase (UDG)

... Note the following when using dU-containing PCR products in downstream applications: PCR products containing dU perform as well as those containing dT when used as hybridization targets or as templates for dideoxy sequencing. PCR products containing dU can be cloned directly, if they are transformed ...
Finding Genes in Eukaryotes
Finding Genes in Eukaryotes

... Usually the primary challenge that follows the sequencing of anything from a small segment of DNA to a complete genome is to establish where the various functional elements such as genes, promoters, terminators etc., lie in the sequence. This module concentrates on the identification of regions of D ...
Chromatin structure - U of L Class Index
Chromatin structure - U of L Class Index

Topic 5 2010 Positional Gene Cloning
Topic 5 2010 Positional Gene Cloning

... can find markers that are the closest to the gene in question. Success depends on having multiple large (if possible) families (so you can score many meioses), good quality information about the phenotype (accurate disease diagnosis) and informative (ideally highly Polymorphic) markers (ones that ar ...
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... Agencourt Ampure XP beads (Beckman Coulter, Brea, CA) and measured by Qubit 2.0 fluorometer (ThermoFisher Scientific, Waltham, MA). The DNA was extracted as previously described.20 The cfDNA was subsequently converted to digital sequence libraries as previously described.20 These digital libraries w ...
NATIONAL UNIVERSITY OF SINGAPORE DEPARTMENT OF BIOLOGICAL SCIENCES ADVANCED PLACEMENT TEST
NATIONAL UNIVERSITY OF SINGAPORE DEPARTMENT OF BIOLOGICAL SCIENCES ADVANCED PLACEMENT TEST

... A. Transformation can occur in the laboratory and in nature. B. Conjugation is the direct transmission of DNA from one bacteria cell to another, but is not a replicative process. C. Plasmid DNA transfer from donor to recipient by conjugation is usually initiated at specific site, known as oriT. D. F ...
Chapter 8
Chapter 8

... The process of DNA replication can be described in 3 steps: 1) Enzymes begin to “unzip” the double helix. This means the hydrogen bonds between the nitrogen bases are broken. When these hydrogen bonds are broken, the two strands separate and each individual base is exposed. Like unzipping a suitcase ...
Name: Date: Period:___ Midterm Review: Study Guide # 4 TOPICS
Name: Date: Period:___ Midterm Review: Study Guide # 4 TOPICS

... 2. Next, scan the objectives for the topic you are about to study in order to get a sense of what you should be focusing your time and energy on. 3. Start mastering each objective by answering the associated review questions right on this sheet. 4. After you have finished, use this sheet as a study ...
U4Word
U4Word

... A. Biological Function: degrade foreign DNA, protect bacterium from phage infection 1. Discovered after the observation that phage that grow in one strain of E coli can not grow in others (restricted growth). The cause of the restriction was identified: REs that cut up phage DNA. 2. Recognition of p ...
Plant DNA Barcoding - Columbia University
Plant DNA Barcoding - Columbia University

... a region of DNA by PCR, also need to select a locus that amplifies reliably, and sequences well. ...
Genomic and cDNA libraries, library screening
Genomic and cDNA libraries, library screening

... Note: ds cDNAs are typically placed in a cloning vector such as bacteriophage lambda (l) or a plasmid ...
Molecular Genetics Part 2 Chapter 19
Molecular Genetics Part 2 Chapter 19

... Chapter 21: The Genetic Basis of Development We will be covering chapter 21 “lightly” – use this guided reading assignment as a roadmap to the topics that we will focus on. 1. What is meant by the phrase “model organisms are representative groups”? ...
Recombinant Paper Plasmids Cut-and
Recombinant Paper Plasmids Cut-and

... yielding “sticky ends,” single strands of nucleotide bases capable of binding with complementary sticky ends. By using enzymes that will cut the DNA on either side of the gene, the gene can be clipped out of the DNA strand. Once scientists obtain the gene they are looking for, they must somehow get ...
PRINCIPLES OF RECOMBINANT DNA TECHNOLOGY
PRINCIPLES OF RECOMBINANT DNA TECHNOLOGY

... DNA when it was recognised that certain enzymes in particular microbes, cleaved DNA at sequence specific sites. These enzymes are called restriction endonucleases and each restriction endonuclease is designated according to the organism from which it was derived. ...
AS 09 Genetic Engineering.pps237.5 KB
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... Enables transcription of mRNA from DNA Cuts DNA at specific base sequences Binds DNA fragments of different origin together ...
PCR (Polymerase Chain Reaction)
PCR (Polymerase Chain Reaction)

... The reaction is carried out in an automated machine, known as a Thermal Cycler, which is capable of rapidly increasing and decreasing the temperature. ...
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... b. Code read 3 letters at a time, each 3 letter “word” known as a codon ...
Ch. 17 DNA to Protein (Transcription and Translation)
Ch. 17 DNA to Protein (Transcription and Translation)

...  The tRNA has a 3 letter message that matches the codon on the mRNA, called the ANTICODON 5. Amino acids get linked together in a “polypeptide chain”, which form a protein 6. The chain folds into a 3-D protein (looks kind of like a 3 leaf clover) *DNA – mRNA – ribosome - amino acids are brought by ...
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Cre-Lox recombination



In the field of genetics, Cre-Lox recombination is known as a site-specific recombinase technology, and is widely used to carry out deletions, insertions, translocations and inversions at specific sites in the DNA of cells. It allows the DNA modification to be targeted to a specific cell type or be triggered by a specific external stimulus. It is implemented both in eukaryotic and prokaryotic systems.The system consists of a single enzyme, Cre recombinase, that recombines a pair of short target sequences called the Lox sequences. This system can be implemented without inserting any extra supporting proteins or sequences. The Cre enzyme and the original Lox site called the LoxP sequence are derived from bacteriophage P1.Placing Lox sequences appropriately allows genes to be activated, repressed, or exchanged for other genes. At a DNA level many types of manipulations can be carried out. The activity of the Cre enzyme can be controlled so that it is expressed in a particular cell type or triggered by an external stimulus like a chemical signal or a heat shock. These targeted DNA changes are useful in cell lineage tracing and when mutants are lethal if expressed globally.The Cre-Lox system is very similar in action and in usage to the FLP-FRT recombination system.
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