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2 edition of Cloning of the variant translocation (14;18)(q32;q21) present in the novel reed-sternberg cell line SBH-1. found in the catalog.

Cloning of the variant translocation (14;18)(q32;q21) present in the novel reed-sternberg cell line SBH-1.

Christine Anne White

Cloning of the variant translocation (14;18)(q32;q21) present in the novel reed-sternberg cell line SBH-1.

by Christine Anne White

  • 340 Want to read
  • 25 Currently reading

Published by National Library of Canada in Ottawa .
Written in English


Edition Notes

Thesis (M.Sc.) -- University of Toronto, 1995.

SeriesCanadian theses = -- Thèses canadiennes
The Physical Object
Pagination1 microfiche : negative. --
ID Numbers
Open LibraryOL17894918M
ISBN 100612076288

Cloning occurs in nature. Identical twins are created when an embryo divides into two individuals with identical DNA. Self-pollinating plants produce plants with the same genetic code. Scientists have been trying to create clones for more than years.   The term translocation is used when the location of specific chromosome material changes. There are two main types of translocations: reciprocal and Robertsonian. In a reciprocal translocation, two different chromosomes have exchanged segments with each other. In a Robertsonian translocation, an entire chromosome attaches to another at the.

Molecular cloning is a method to prepare a recombinant DNA molecule, an extra-chromosomal circular DNA that can replicate autonomously within a microbial host. DNA ligation is commonly used in molecular cloning projects to physically join a DNA vector to a gene of interest. ­The ­main reason to clone plants or animals is to mass produce organisms with desired qualities, such as a prize-winning orchid or a genetically engineered animal -- for instance, sheep have been engineered to produce human you had to rely on sexual reproduction (breeding) alone to mass produce these animals, then you would run the risk of breeding out the desired traits because.

Molecular cloning is a set of methods, which are used to insert recombinant DNA into a vector - a carrier of DNA molecules that will replicate recombinant DNA fragments in host organisms. The DNA fragment, which may be a gene, can be isolated from a prokaryotic or eukaryotic specimen. Following isolation of the fragment of interest, or insert.   In biology, translocation refers to two completely different processes. In botany, or the study of plants, translocation is the movement of material from one place to another within a plant. In genetics, it is the exchange of parts between two this article, we are going to be looking at chromosomal translocation specifically.


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Cloning of the variant translocation (14;18)(q32;q21) present in the novel reed-sternberg cell line SBH-1 by Christine Anne White Download PDF EPUB FB2

In genetics, chromosome translocation is a phenomenon that results in unusual rearrangement of chromosomes. This includes balanced and unbalanced translocation, with two main types: reciprocal- and Robertsonian translocation. Reciprocal translocation is a chromosome abnormality caused by exchange of parts between non-homologous detached fragments of two different.

Genetically, markers on nonhomologous chromosomes appear to be linked if these chromosomes take part in a translocation and the loci are close to the translocation breakpoint. Figure shows a situation in which a translocation heterozygote has been established by crossing an a/a ; b/b individual with a translocation homozygote bearing the wild-type alleles.

The variant translocation reappeared with additional chromosomal abnormalities including Ph duplication. This clone with variant Ph translocation appeared to have been eradicated by BMT (the patient reached complete molecular response with RQ-PCR), however, it reappeared 16 months later causing relapse into the myeloid blastic by: 8.

TA cloning is one of the simplest forms of cloning. In this method, vectors containing 5' thymine overhangs are used to accept PCR products in which additional 3' adenosine overhangs have been added on by the nature of TAQ polymerase amplification.

TA cloning has the advantage of ease and speed, since no restriction digestion step is required. Cloning, the process of generating a genetically identical copy of a cell or an organism.

Cloning happens often in nature, as when a cell replicates itself asexually without genetic alteration or recombination. Learn more about cloning experiments, cloning techniques, and the ethics of human reproductive cloning.

Rather than representing a random event, recent studies indicate that chromosomal translocation is a non-random event in a spatially regulated, site-specific, and signal-driven manner, reflecting actions involved in transcriptional activation, epigenetic regulation, three-dimensional nuclear architecture, and DNA damage-repair.

The translocation frequency was calculated using the equation, q = 1 - (1-p)1/n; n = number of haploid genomes per aliquot, p = the probability that an aliquot contains a translocation product, and q = the probability that one randomly selected haploid genome in a given aliquot sustained a translocation.

The gel images indicate results of the PCR. @article{osti_, title = {Familial translocation involving chromosomes 1 and 9 in a patient with Philadelphia-positive CML}, author = {Rehman, K and Rosner, F and Shanske, A}, abstractNote = {CML has provided a model for understanding the genetic basis of neoplasia.

Approximately 5% of Philadelphia-positive patients have a variant chromosome rearrangement. CLONING AND EXPRESSION OF WILD-TYPE AND MUTATED FORMS OF BCR-ABL IN A MOUSE PRO-B CELL LINE By Stine Gangnæs Hammer Department of Pharmacology, Institute of Pharmacy Faculty of Medicine translocation and results in the constitutively activated Bcr-Abl tyrosine kinase.

Since the tyrosine kinase activity of the Bcr-Abl fusion protein is the. The genetic loci involved in the chromosomal breaksites are: switch sequences and some non-switch regions near JH on chromosome 12; the 5′ region of c-myc proto-oncogene beginning bp 5′ of exon-1 and extending into intron-1 on chromosome 15; the Igκ light chain locus on chromosome 6 and Pvt-1 (PCT variant translocation) locus some Molecular cloning of a translocation breakpoint hotspot in 22q11 Article (PDF Available) in Genome Research 17(4) May with 59 Reads How we measure 'reads'.

Basic Steps of Gene Cloning 4) When the host cell divides, copies of the recombinant DNA molecule are passed to the progeny and further vector replication takes place.

5) After a large number of cell divisions, a colony, or clone, of identical host cells is produced. Each cell in the clone contains one.

Cloning is the process of producing genetically identical individuals of an organism either naturally or artificially. In nature, many organisms produce clones through asexual g in biotechnology refers to the process of creating clones of organisms or copies of cells or DNA fragments (molecular cloning).Beyond biology, the term refers to the production of multiple copies of.

Novel translocation variant in ewing sarcoma involving the NFATc2 gene Article in Cancer Genetics and Cytogenetics (1) November with 44 Reads How we measure 'reads'. Cloning may involve cloning small DNA fragments (molecular cloning), or cloning entire organisms (reproductive cloning).

In molecular cloning with bacteria, a desired DNA fragment is inserted into a bacterial plasmid using restriction enzymes and the plasmid is taken up by a bacterium, which will then express the foreign : Charles Molnar, Jane Gair, Molnar, Charles, Gair, Jane.

Steps in cloning a single piece of DNA 1. Appropriate restriction sites 2. Cut vector and foreign DNA with RE 3. Run on gel to separate fragments 4.

Isolate specific fragment 5. Ligate with cut vector 6. Transform host bacteria. Selection. Grow up colonies. Isolate plasmid DNA. Cut with RE to confirm presence of foreign DNA.

File Size: 5MB. A child with an unbalanced translocation causing a physical or mental handicap Unbalanced translocation means that there is extra or missing chromosomal material; Could lead to physical differences, medical problems like heart defects, etc. An unbalanced translocation that leads to miscarriage or stillbirth.

Prader-Willi syndrome (MIM #; PWS) is caused by lack of the paternally-derived copies, or their expression, of multiple genes in a 4 Mb region on chromosome 15q Known mechanisms include large deletions, maternal uniparental disomy or mutations involving the imprinting center.

De novo balanced reciprocal translocations in 5 reported individuals had breakpoints Cited by: Proposed translocation rules I 1) Order of breakpoint descriptions follows ISCN rules • Sex chromosome(s) first, X before Y • Autosomes: low to high number • der(X) > der(Y) > der(1) > > der(22) • der number depends on chromosomal origin intact centromere Format translocation description:File Size: KB.

Translocations are chromosome mutations in which chromosome segments, and the genes they contain, change positions. Translocations can occur within a chromosome (intrachromosomal) or between chromosomes (interchromosomal). In an intrachromosomal translocation, a segment breaks off the chromosome and rejoins it at a different location.

Two types of interchromosomal translocations are. Structural variations (SVs), including translocations, inversions, deletions and duplications, potentially lead to human genetic diseases arising from disruption and dosage changes of functionally Cited by: Cloning - Cloning - Reproductive cloning: Reproductive cloning involves the implantation of a cloned embryo into a real or an artificial uterus.

The embryo develops into a fetus that is then carried to term. Reproductive cloning experiments were performed for more than 40 years through the process of embryo splitting, in which a single early-stage two-cell embryo is manually divided into two.

The most common cloning method is called nuclear transfer and involves taking the nucleus from an egg cell, replacing it with the nucleus from a cell of the animal to be cloned, and then.