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Lecture notes - Cell And Molecular Biology (DNA techenology) - Using Becker's World of the Cell, Global Edition

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If you're studying a life science (e.g. - biomed, bioscience, physiology, sports science, sports physiology etc), then this detailed set of lecture notes on DNA technology will help you smash your first set of exams on cell/molecular biology! These notes cover DNA technology and Next generation sequencing. It's advised you use these along with the other 2 DNA lecture notes (on structure, genes and replication) You'll need an in depth knowledge of DNA technology throughout your degree. In your final year, if you choose to write your thesis in the field of DNA (e.g. - a potential treatment for cancer) - an in depth understanding of DNA technology will be expected of you so this set of notes will be invaluable to you not just in first year, but also in your second and final year as well!

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DNA Technology 4/11/19
Karyotype = complete set of all chromosomes of a cell of a living organism

Chromosomes have bands

3 X chromosome 21 = Down Syndrome

Chromosomal numerical abnormalities can occur

- Aneuploidy = Extra chromosomes – often lethal
- Missing Chromosomes

Chromosomal rearrangements can occur – often due to breakage in DNA double helix at 2 different
locations – re-joining of broken ends = new arrangement of genes

In situ Hybridization = Nucleic acid hybridization (Annealing of single strands) with labelled probe –
detects location of specific mRNA in particular organism

E.g. – of Fluorescence in situ Hybridization (FISH)

RFLP = Restriction Fragment Length Polymorphism

- Relies on use of Restriction enzymes/endonucleases – cut DNA at specific locations
- Protect bacterial cells by cutting foreign DNA from other organisms/phages
- Recognises specific DNA seq./site – cuts both strands at said site

SNP = Substitution of single nucleot. – at specific location of genome




Gel electrophoresis:
After Recombinant Plasmid = copied in host cell – fragments can be cut out again – and separated
and visualised by Gel electrophoresis.

- Gel = polymer – separates fragments by length
- Gel = in aq. and buffered solution – current = on
- DNA = -ve charge – moves to +ve cathode
- Longer fragments move slower – more resistance with gel
- DNA binding dye = added – pink in UV light – current = off
- Bands of the same length will be seen together




PCR:
- In Vitro process – outside organism
- Amplifies DNA
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