Sam:LabNotes/Microbione/2009-2-3: Difference between revisions
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>Sam Chiang |
>Sam Chiang |
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(11 intermediate revisions by the same user not shown) | |||
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==Objective== | ==Objective== | ||
Beside the realtime monitoring, | |||
#Design 18S primers for positive control / validation purpose of a successful MDA reaction using human genome template. | #Design 18S primers for positive control / validation purpose of a successful MDA reaction using human genome template. | ||
#Design 16S primers for positive control / validation purpose of a successful MDA reaction using bacteria genome template. | #Design 16S primers for positive control / validation purpose of a successful MDA reaction using bacteria genome template. | ||
#These primers could also be used to detect the contamination of exogenus gDNA. | #These primers could also be used to detect the contamination of exogenus gDNA. | ||
==Human S18 primer== | ==Human S18 primer== | ||
Line 22: | Line 21: | ||
#Using Netprimer[http://www.premierbiosoft.com/netprimer/index.html]to evaluate primer structure. | #Using Netprimer[http://www.premierbiosoft.com/netprimer/index.html]to evaluate primer structure. | ||
#Pick up two primers with differnt size of amplicon. | #Pick up two primers with differnt size of amplicon. | ||
>h18S_211_f | >h18S_211_f | ||
TTGCTGCAGTTAAAAAGCTC | TTGCTGCAGTTAAAAAGCTC | ||
>h18S_211_r | >h18S_211_r | ||
CATTATTCCTAGCTGCGGTA | CATTATTCCTAGCTGCGGTA | ||
Line 32: | Line 31: | ||
CGACTACCATCGAAAGTTGA | CGACTACCATCGAAAGTTGA | ||
----------------------------------------------- | ----------------------------------------------- | ||
*[[Human 18S rRNA gene primer | *[[Media:Human 18S rRNA gene primer design.doc|Human 18S rRNA gene primer design]] | ||
==Bacteria S16 primer== | |||
#Use the reported 16S primers which has been tested on conserved region of 16S gene[[Media:Soni_E coli 0157 and AI-2_2008.PDF| (citaiton of 16S primer)]]. | |||
#Primer sequences have been test on '''UCSD prokaryote genome browser'''[http://archaea.ucsc.edu/cgi-bin/hgGateway?org=Salmonella+typhimurium+LT2&db=salmTyph_LT2&hgsid=182679]. All of primers were able to match most E. coli stains' 16S gene region. | |||
'''Primer sequences''' | |||
>Pilli_16S_f | |||
CCAGCAGCCGCGGTAAT | |||
>Pilli_16S_r | |||
TGCGCTTTACGCCCAGTAAT | |||
---------------------------------------------- | |||
>Dowd_16S-1-f | |||
TCCTACGGGAGGCAGCAGT | |||
>Dowd_16S-1-r | |||
GGACTACCAGGGTATCTAATCCTGTT | |||
---------------------------------------------- | |||
>Dowd_16S-2-f | |||
CGCTAGTAATCGTGGATCAGAATG | |||
>Dowd_16S-2-r | |||
TGTGACGGGCGGTGTGTA | |||
*[[Media:16S primers.doc|16S primers condition]] |
Latest revision as of 18:34, 9 February 2009
Primer design for human 18S and Bacteria 16S[edit]
Objective[edit]
Beside the realtime monitoring,
- Design 18S primers for positive control / validation purpose of a successful MDA reaction using human genome template.
- Design 16S primers for positive control / validation purpose of a successful MDA reaction using bacteria genome template.
- These primers could also be used to detect the contamination of exogenus gDNA.
Human S18 primer[edit]
- Collect the human S18 cDNA sequence
- Clean the sequcne and mask the inconsistat nucleotide
- Paste the sequence on KZ's Primer3 calculator[1]
- Criteria:
Primer size: Min: 18bp, opt:20 bp, Max: 22bp Product size: ~200 bp; ~300 bp Annealing Temp: Min:57, Opt:58, Max:59
Results
- Using Netprimer[2]to evaluate primer structure.
- Pick up two primers with differnt size of amplicon.
>h18S_211_f TTGCTGCAGTTAAAAAGCTC >h18S_211_r CATTATTCCTAGCTGCGGTA ----------------------------------------------- >h18S_306_f GTACAGTGAAACTGCGAATG >h18S_306_r CGACTACCATCGAAAGTTGA -----------------------------------------------
Bacteria S16 primer[edit]
- Use the reported 16S primers which has been tested on conserved region of 16S gene (citaiton of 16S primer).
- Primer sequences have been test on UCSD prokaryote genome browser[3]. All of primers were able to match most E. coli stains' 16S gene region.
Primer sequences
>Pilli_16S_f CCAGCAGCCGCGGTAAT >Pilli_16S_r TGCGCTTTACGCCCAGTAAT ---------------------------------------------- >Dowd_16S-1-f TCCTACGGGAGGCAGCAGT >Dowd_16S-1-r GGACTACCAGGGTATCTAATCCTGTT ---------------------------------------------- >Dowd_16S-2-f CGCTAGTAATCGTGGATCAGAATG >Dowd_16S-2-r TGTGACGGGCGGTGTGTA