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Biotechnology Webquest
Biotechnology Webquest

... In 2002, David Duncan became what is believed to be the first healthy human screened for all the known genetic markers for disease. He was a test subject for a biotech startup called Sequenom in San Diego. In the end, he was told he had a gene that put him at a greater risk for developing heart dise ...
Amsterdam 2004
Amsterdam 2004

... • computer science: an ontology is a data model that represents a domain and is used to reason about the objects in that domain and the relations between them. – GO:0008150 : biological_process – GO:0005575 : cellular_component – GO:0003674 : molecular_function ...
HONORS BIOLOGY FINAL EXAM STUDY GUIDE 2010
HONORS BIOLOGY FINAL EXAM STUDY GUIDE 2010

... meiosis? Provide a specific example of a human genetic disorder resulting from non-disjunction. 5. Dr. Goldin cuts her big toe. What cellular division process would be used to repair the damage? What other cells in her body would have the same chromosome number? 6. What does it mean to be “haploid”? ...
E. coli - Sonoma Valley High School
E. coli - Sonoma Valley High School

... 5. Offspring will contain one chromosome with the gene of interest knocked out. Genetic crosses can then produce mice homozygous for the knocked out gene to assess the phenotype. This can range from lethality to no visible effect depending on the gene. ...
Quiz Questions - The University of Sheffield
Quiz Questions - The University of Sheffield

... B.  Disulphide bonds –S-S- may be created by oxidising pairs of -SH groups. C.  Branched polysaccharide chains can be built up on the side-chain nitrogen of asparagine. D.  Peptide bonds may be selectively cleaved. E.  An isopeptide linkage can be formed between the εNH2 group of a lysine and the C- ...
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Document

...  all living organisms are built out of proteins ...
Central Dogma - Arkansas State University
Central Dogma - Arkansas State University

... interactions between the DNA, mRNA, and polymerase; U-A basepairs are very weak, and the complex falls apart. ...
Taxonomy employs a hierarchical system of classification
Taxonomy employs a hierarchical system of classification

... – Systematists may compare hundreds or thousands of adjacent nucleotide positions and among several DNA regions to assess the relationship between two species. – This DNA sequence analysis provides a quantitative tool for constructing cladograms with branch points defined by mutations in DNA sequenc ...
Biology- Semester 2 Final Exam Review 2012
Biology- Semester 2 Final Exam Review 2012

... State two laws of heredity that were developed from Mendel’s work. Differentiate genes from alleles. How did Mendel’s F1 generation plants differ from his F2 generation plants? Many inherited disorders of humans appear in children of parents who do not have the disorder. How can you explain this? 6. ...
early RNs, crossing over initiates, then synapsis begins Chiasmata
early RNs, crossing over initiates, then synapsis begins Chiasmata

... •Ac transposable element is autonomous: it encodes the gene for the transposase enzyme that allows it to jump. Some maize lines have active Ac. •Ds element is non -autonomous: it is a derivative of Ac but its transposase gene does not function. However, when Ac is present in same genome, Ds can jump ...
C2005/F2401 `09
C2005/F2401 `09

... the genotype (the DNA) without changing the phenotype (the function or appearance). B-2. AUG to AUA is missense – it changes the amino acid from met to ile. UAC to UAA causes a change but it is nonsense, not missense – it creates a premature stop codon. B-3. See the code table. The two correct choic ...
HRB/MRCG 2011/7 Genome-wide DNA methylation analysis of
HRB/MRCG 2011/7 Genome-wide DNA methylation analysis of

... Unique methylation changes were found in the brain of patients with TLE as well as according to pathology. An analysis of what the genes do found many to be involved in brain development and structure, neurotransmission, cell death and DNA transcription. We also identified methylation changes to wha ...
16. Nuclear gene organization
16. Nuclear gene organization

... 4. Pseudogenes: Two types  versions of genes that have become inactivated, such as some alpha and beta globin genes.  Retroposons or processed pseudogenes: copies of mRNAs from functional genes that are reinserted into the chromosome. o Usually not expressed and contain multiple mutations. o Fig. ...
S1 Supplementary information.
S1 Supplementary information.

... CD4-3200bp substrate. Examples of end-joining intermediates in C-NHEJ (left panel), which are KU/Lig4-dependant and A-EJ (right panel), which are KU/Lig4-independant. Upper panel: the structure of the I-SceI cleavage site (bold type indicates the four 3’-protruding nucleotides generated by I-SceI cl ...
Chapter 17 – Molecular genetics
Chapter 17 – Molecular genetics

... •The two original strands of DNA are shown in yellow (light); newly synthesized DNA is blue (dark) • Conservative replication would leave intact the original DNA molecule and generate a completely new molecule. • Dispersive replication would produce two DNA molecules with sections of both old and ne ...
Basic Premises of Population Genetics
Basic Premises of Population Genetics

Chapter Outline
Chapter Outline

... a. An exon is a protein-coding region of the DNA code in the pre-mRNA transcript eventually expressed in the final polypeptide product. b. An intron is a non-protein coding region of DNA removed by “self-splicing” or spliceosomes before the mRNA leaves the nucleus. 5. Ribozymes are enzymes made of ...
DNA, Genes, and Chromosomes
DNA, Genes, and Chromosomes

... varying lengths are called genes. Each gene contains a piece of genetic information that tells the cell to make a specific protein. Thousands of genes are found on each strand of DNA that makes up your chromosomes. It had been thought that much of the length of DNA does not seem to code for any spec ...
Agrobacterium tumefaciens
Agrobacterium tumefaciens

... Often one desires to insert foreign DNA in a particular orientation  This can be done by making two cleavages with two different restriction enzymes  Construct foreign DNA with same two restriction enzymes  Foreign DNA can only be inserted in one direction ...
Method of localizing, either mRNA within the cytoplasm or DNA
Method of localizing, either mRNA within the cytoplasm or DNA

... RNase treatment pre-hybridization Addition of an excess of unlabeled probe Hybridization with sense probe Tissue known not to express the gene of interest ...
LIGATION AND TRANSFORMATION
LIGATION AND TRANSFORMATION

... Two crucial procedures in cloning are the ligation of the foreign DNAs to the vector DNA and the transformation of bacteria using those ligated DNA constructs (the recombinant molecules). Ligation is accomplished using the enzyme DNA ligase (usually from the bacteriophage T4). It requires ATP and ma ...
Figure 1 - genomics-lab
Figure 1 - genomics-lab

... (P1 being for instance allele specific), a third primer, P3 is designed to bind specifically to a site on the target sequence downstream of the P1 binding. P3 is labeled with two fluorophores, a reporter dye (R) is attached at the 5' end, and a quencher dye (D), which has a different emission wavele ...
Ch. 12 DNA - Fort Bend ISD
Ch. 12 DNA - Fort Bend ISD

... DNA replication Watson and Crick’s model of DNA became a quick success because it revealed the mechanism by which DNA can copy itself.  Each strand of DNA can be used to make another strand. Because of this we say that DNA is “complementary”.  Replication: The process of duplicating DNA ...
Chapter 13, 14 Rev
Chapter 13, 14 Rev

... The sequence of nitrogenous bases on one strand of DNA may determine the sequence of: a. Fatty acids in a fat molecule b. Amino acids in a protein molecule c. Sugars in a polysaccharide molecule d. All of the above choices are correct e. Bases in a protein molecule The sequence of nitrogen bases on ...
Gel Electrophoresis!
Gel Electrophoresis!

... • All cells have the same DNA • All multicellular organisms begin as a group of unspecialized cells = stem cells – No particular function ...
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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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