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Basics of Tics
Basics of Tics
Dr: A. Ellethy
College of Dentistry
Lec. 2
1 4 3 1
Top secretes to study DNA sequences
• What, why, when, where study gene?
• How to design a primer?
• Types of practical used primers
• How to read DNA sequences (the most recently
developed program in USA).
• Data analysis for sequenced DNA
What,
why,
when,
where
study
gene?
WHERE IS DNA? WHY?
Under sterile conditions
Radioisotopes S35
Fluorescently labeled
PCR PROGRAME
30 cycles:
Denaturation 97°C 1 min
Annealing X°C 1 min’
Extension 72°C 1min
1 cycle:
72°C 6 min
store:
4°C store
4 hours run 2
-------------------?
How
seq aut
uen om
ces ate
? d
seq
u en
c er
wo
rk
for
DN
A
DNA CHROMAS
Open and save sequences in Applied Biosystems, Staden Chromatogram (SCF), FASTA,
EMBL, GenBank, SwissProt, GenPept, GCG RSF and plain text formats.
HOW TO USE DNA CHROMAS?
Cell Chromosome DNA
DNA SEQUENCE
ANALYSIS
IDENTIFICATION
CONFIRMATION
APPLICATION
DIAGNOSIS
VACCINATION
REPAIRING
Dentin Sialophosphoprotein EST
ATGGTCTTATTAAGAAAAAACTTCTGTTGTACCATAGGTTATGCCCATATTTCCTCCACCACAACTTCAA
ATCCTTCATCAGAAACGAAGAGCATAGCCACAGACTATGAAACCACCCCGACCACCACTATATCTAGCAC
TGCCTCAGGATCTACGCCCACCCTGACCACCACTGCATCCAGCATTGCCTCAGACTCTAAGCCCACCCTG
ACCACCACTGCATCCAGCACTGCCTCAGGATCTATGTCCACCCCGACCACCCCTGCATCCAGCACTGCCT
CAGGCTCTACACCCACAACGACCACCACTGCATCCAGCACTGCCTCAGGATCTACACCTACCCCGACCAC
TACTGCATCTAGCAAAGCCTCAAGATCTGTGCCCACCACTGTATCCAGCACTGGCTCAGGCTCTACACCC
ACTCCGACCACCACTGCATCCAGCACTGCCTCAGGATCTACGCCCACCCTGACCACCACTCCATCCAGCA
CTGCCTCAGGATCTACACCTACCCCGACCACCCCTGCATCCAGTACTGCCTCAAGCTCTTCACCCACCCC
AACCACCCCTGTATCCAGCACTGCCTCAGGATCTACACCCACCCCGACCACCACTGCATCTAGCAAGGCC
TCAGGATCTGTGCCCACCACTGTATCCAGCACTGGCTCAGGCTCTACACCCACTCTGACCACCACTGTAT
CCAGCACTGTCTCAGACTCTACACCCACCCCGACCACCACTGCATCCAGCACTGCCTCAGGATCAGCACC
CACCCCGACCACCACTGCATCTAGCACTGCCTCAGGATCTATGCCCACCCTGACCACCAATGCATCCAGC
Put original DNA sequences