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XIANG Hua
XIANG Hua

DNA Duplications and Deletions Help Determine Health
DNA Duplications and Deletions Help Determine Health

High Throughput Screening of Single Nucleotide Polymorphisms
High Throughput Screening of Single Nucleotide Polymorphisms

RayBio Genomic DNA Magnetic Beads Kit
RayBio Genomic DNA Magnetic Beads Kit

DNA structure and replication_AP Bio
DNA structure and replication_AP Bio

... telomeres. • Telomerase uses a short molecule of RNA as a template to extend the 3’ end of the telomere. – There is now room for primase and DNA polymerase to extend the 5’ end. – It does not repair the 3’-end “overhang,” but it does lengthen the telomere. ...
File
File

... the cell cycle 2. nucleus 3. S stage 4. so that every cell will have a complete set of DNA following cell division 5. something that serves as a pattern 6. ATCCATG 7. Proteins help unzip the DNA strand, hold the strands apart, and bond nucleotides together. 8. hydrogen bonds connecting base pairs 9. ...
Sequencing the World of Possibilities for Energy & Environment
Sequencing the World of Possibilities for Energy & Environment

... Sequencing the World of Possibilities for Energy & Environment ...
slides
slides

... –  coding  region,  intron  region,  promoter  site   Ease  of  genotyping  (high-­‐throughput  genotyping)   Less  mutable  than  other  forms  of  polymorphisms   SNPs  account  for  around  90%  of  human  genomic  varia@on   About  10  mi ...
Phenotype Sequencing - Bioinformatics Research Group
Phenotype Sequencing - Bioinformatics Research Group

Guidance on the significance of chemical
Guidance on the significance of chemical

... long periods of time between mutation and onset of disease make it very difficult to investigate the role of chemical-induced mutation in human disease. ...
Molecular analysis of genebanks for sustainable conservation and increased useo f crop genetic resources
Molecular analysis of genebanks for sustainable conservation and increased useo f crop genetic resources

... showing genetic variability for drought tolerance. For this purpose, the following steps should be considered: (a) genetic maps making ample use of molecular markers (especially microsatellite or STRs) are constructed in order to locate genomic regions (QTLs) associated with the control of drought t ...
Organic Chemistry Fifth Edition
Organic Chemistry Fifth Edition

... The nucleotide sequence in regions of DNA that code for proteins varies little from one individual to another, because the proteins are the same. Most of the nucleotides in DNA are in "noncoding" regions and vary significantly among individuals. Enzymatic cleavage of DNA give a mixture of polynucleo ...
Comparison of genes among cereals
Comparison of genes among cereals

... gene homologue in a non-orthologous location [7,25]. The putative mechanism for this phenomenon is an ancient gene duplication in the common ancestor followed by the loss of one gene copy in the first modern species and the loss of the other copy in the second species. A second example of gene d ...
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... cell biologists photograph cells in mitosis, when the chromosomes are fully condensed and easy to view. ...
Gene Transfer
Gene Transfer

... of the β-lactamase protein if successfully transformed into suitable bacteria. In the presence of the ampicillin, the transformed bacteria would have a strong selective advantage over susceptible bacteria. The looping out of DNA could occur by homologous recombination within the chromosome between a ...
Current Microbiology
Current Microbiology

... reflect only a homology at the primer binding site. Thus, this result indicated that B. thuringiensis isolate BR30 carried cry1I-type genes differing from known cry1I genes, at least in the binding sites of the primers cry5A and/or cry5B. From the strain BR30, we have cloned a new cry1I-type gene, c ...
Technical Note
Technical Note

... Uniquely tagging input fragments with molecular barcodes enables the counting of molecules post-sequencing. The MBC allows precise counting of the unique fragments that originate from the loci targeted by the panel. The number of unique MBCs associated with each target region is used to deduce copy ...
Chapter 9 - Advanced Biology
Chapter 9 - Advanced Biology

... ◦ Cutting the chromosome # in half makes it so that 2 parents can produce an offspring that is genetically unique, but still maintains the overall chromosome # for that species ...
Synthetic Biology: Gene Transformation and Protein Purification
Synthetic Biology: Gene Transformation and Protein Purification

... • The insertion of new DNA into a host cell to give the cell the ability to produce new proteins and new traits. • Transformation can be used for: – Agriculture: plants become more resistant to pests, ...
2009 exam 3
2009 exam 3

... A. The initiator tRNA could be in (the P site) (the A site) (the E site) (A or P) (A or E) (E or P) (any of these). B. Methionine should be attached directly to (tRNA #1) (AA #2 = amino acid #2) (tRNA #2) (AA #3) (peptidyl transferase) (either tRNA) (tRNA or AA #2) (either AA) (none of these) (any o ...
Changes in DNA and results of changes
Changes in DNA and results of changes

... Components of DNA and how DNA relates to traits 1. The structures marked 3 in the diagram are responsible for – a. Absorbing oxygen b. Carrying genetic codes c. Lining up amino acids d. Serving as an anticodon 2. Why will knowledge of the human genome enable scientists to better understand proteins ...
2013 Training Handout
2013 Training Handout

... into a piece of DNA used to transfer the genes or vector which is inserted to a Host cell (often a bacterium)  Plasmids– in bacteria, circular DNA serve as vectors. Easily taken up by bacterial cells. It is more difficult to insert vector into Eukaryotic cells.  Transgenic organisms have DNA from ...
One Shot PIR1 and PIR2 - Thermo Fisher Scientific
One Shot PIR1 and PIR2 - Thermo Fisher Scientific

... Spread 20 µl to 200 µl from each transformation vial on separate, labeled LB agar plates containing the appropriate antibiotic. Note: We recommend that you plate two volumes to ensure that one plate will have well-spaced colonies. For plating small volumes, add 20 µl SOC to allow even spreading. ...
DNA Technology Notes (13.1 &13.2)
DNA Technology Notes (13.1 &13.2)

...  Biologists use DNA technology to produce plants with many desirable traits.  Genetically engineered cotton resists insect infestation of the bolls.  Sweet-potato plants are resistant to a virus that could kill most of the African harvest.  Rice plants with increased iron and vitamins ...
1 Comp. Funct. Genom. Copyright © (2002) John Wiley & Sons, Ltd.
1 Comp. Funct. Genom. Copyright © (2002) John Wiley & Sons, Ltd.

... genes and proteins based on shared biology. It will also aid the interpretation of large datasets created by functional genomics projects [6]. The majority of eukaryotic genome projects already use the GO annotation system, and GO annotations are being incorporated into SWISSPROT and GeneDB (see sec ...
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Genomic library



A genomic library is a collection of the total genomic DNA from a single organism. The DNA is stored in a population of identical vectors, each containing a different insert of DNA. In order to construct a genomic library, the organism's DNA is extracted from cells and then digested with a restriction enzyme to cut the DNA into fragments of a specific size. The fragments are then inserted into the vector using DNA ligase. Next, the vector DNA can be taken up by a host organism - commonly a population of Escherichia coli or yeast - with each cell containing only one vector molecule. Using a host cell to carry the vector allows for easy amplification and retrieval of specific clones from the library for analysis.There are several kinds of vectors available with various insert capacities. Generally, libraries made from organisms with larger genomes require vectors featuring larger inserts, thereby fewer vector molecules are needed to make the library. Researchers can choose a vector also considering the ideal insert size to find a desired number of clones necessary for full genome coverage.Genomic libraries are commonly used for sequencing applications. They have played an important role in the whole genome sequencing of several organisms, including the human genome and several model organisms.
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