Team:MIT/sequences

From 2008.igem.org

(Difference between revisions)
(→P23: Reverse Primer for BBa_I13521)
(→Primers)
 
Line 223: Line 223:
**GC content = 53.7%
**GC content = 53.7%
**melting temp = 68.9 C
**melting temp = 68.9 C
 +
 +
===P24: bbRBSfw: attach RBS upstream of p1025 part, with BB end===
 +
[[Image:P24.jpg]]
 +
**sequence = GGAATTCGCGGCCGCTTCTAGAGTC...?
 +
**length = ? bp
 +
**GC content = ?%
 +
**melting temp = 69.4 C
 +
 +
===P25: expfw: attach NdeI end to beginning of p1025 part===
 +
[[Image:P25.jpg]]
 +
**sequence = GGAATTCCATATGCAGAAGAAAAA...?
 +
**length = ? bp
 +
**GC content = ?%
 +
**melting temp = 61.3 C
 +
 +
===P26: exprev: attach XhoI end after p1025 part===
 +
[[Image:P26.jpg]]
 +
**sequence = CCGCTCGAGTTATTAGTGGTGATG...?
 +
**length = ? bp
 +
**GC content = ?%
 +
**melting temp = 63.5 C
==Plasmids==
==Plasmids==

Latest revision as of 19:00, 13 August 2008


Home The Team The Project Parts Submitted to the Registry Modeling Notebook


Contents

Primers

  • All BioBrick parts are Phillips-Silver to enable fusion peptide construction


P1: Forward Primer for Promoter

P1-2.jpg

    • foward sequence: CCG CTT CTA GAG TAA TAC GAC TCA CTA TAG GGA ATA CAA GCT ACT TGT TCT TTT TGC ATA CTA GAG ATT AAA GAG GAG AAA TAC TAG ATG CAG AAG AAA AAA TCC GC
    • length = 107 bp
    • GC content = 37.4 %
    • melting temp = 68.9 ºC
    • concentration:
      • original:
      • dilute: 5uM

P2: Reverse Primer for Peptide

P2.jpg

    • reverse sequence: GTT CTT CTC CTT TAC GCA TGC TGC CCC CGC CGC TGC CGC C
    • length = 40 bp
    • GC content = 67.5 %
    • melting temp = 74.7 ºC
    • concentration:
      • original:
      • dilute: 5uM

P3: Forward Primer for GFP

P3.jpg

    • forward sequence: GGC GGC AGC GGC GGG GGC AGC ATG CGT AAA GGA GAA GAA C
    • length = 40 bp
    • GC content = 67.5 %
    • melting temp = 74.7 ºC
    • concentration:
      • original:
      • dilute: 5μM

P4: Reverse Primer for GFP

P4-5.jpg

    • sequence: CTG CAG CGG CCG CTA CTA GTA AGA GAA TAT AAA AAG CCA GAT TAT TAA TCC GGC TTT TTT ATT ATT TTT ATT AGT GGT GAT GGT GAT GAT GTT TGT ATA GTT CAT CCA TGC
    • length = 111 bp
    • GC content % = 36.0 %
    • melting temp = 69.6 ºC
    • concentration =


P5: Reverse Primer for GFP without Terminator

P5.jpg

    • sequence: CTG CAG CGG CCG CTA CTA GTA TTA TTA GTG GTG ATG GTG ATG ATG TTT GTA TAG TTC ATC CAT GC
    • length = 65bp
    • GC content = 44.6 %
    • melting temp = 68.5 ºC
    • concentration:


P6: Forward Primer for BioBrick FLAG tag

P6.png

    • sequence: GAATTCGCGGCCGCTTCTAGAGACTACAAAGACGACGACGACAAAACTAGTAGCGGCCGCTGCAG
    • length = 65bp
    • GC content = 55.4%
    • melting temp = 72.1 ºC
    • concentration =


P7: Reverse Primer for BioBrick FLAG tag

P7.png

    • sequence: CTGCAGCGGCCGCTACTAGTTTTGTCGTCGTCGTCTTTGTAGTCTCTAGAAGCGGCCGCGAATTC
    • length = 65bp
    • GC content = 55.4%
    • melting temp = 72.1 ºC
    • concentration =


P8: Forward Primer for BioBrick HA tag

P8.png

    • sequence: GAATTCGCGGCCGCTTCTAGATACCCGTACGACGTTCCGGACTACGCTACTAGTAGCGGCCGCTGCAG
    • length = 68bp
    • GC content = 60.3%
    • melting temp = 73.4 ºC
    • concentration =


P9: Reverse Primer for BioBrick HA tag

P9.png

    • sequence:CTGCAGCGGCCGCTACTAGTAGCGTAGTCCGGAACGTCGTACGGGTATCTAGAAGCGGCCGCGAATTC
    • length = 68bp
    • GC content = 60.3%
    • melting temp = 73.4 ºC
    • concentration =


P10: Forward Primer for BioBrick His tag

P10.png

    • sequence: GAATTCGCGGCCGCTTCTAGACATCATCACCATCACCACACTAGTAGCGGCCGCTGCAG
    • length = 59bp
    • GC content = 57.6%
    • melting temp = 72.7 ºC
    • concentration =


P11: Reverse Primer for BioBrick His tag

P11.png

    • sequence: CTGCAGCGGCCGCTACTAGTGTGGTGATGGTGATGATGTCTAGAAGCGGCCGCGAATTC
    • length = 59bp
    • GC content = 57.6%
    • melting temp = 72.7 ºC
    • concentration =


P12: Forward Primer for BioBrick TEV protease cut site

P12.png

    • sequence: GAATTCGCGGCCGCTTCTAGAGAAAACCTGTACTTCCAGGGTACTAGTAGCGGCCGCTGCAG
    • length = 62bp
    • GC content = 56.5%
    • melting temp = 72.2 ºC
    • concentration =


P13: Reverse Primer for BioBrick TEV protease cut site

P13.png

    • sequence: CTGCAGCGGCCGCTACTAGTACCCTGGAAGTACAGGTTTTCTCTAGAAGCGGCCGCGAATTC
    • length = 62bp
    • GC content = 56.5%
    • melting temp = 72.2 ºC
    • concentration =


P14: Forward Primer for BioBrick pRT B l.bulgaricus signal sequence

P14.png

    • sequence = GAATTCGCGGCCGCTTCTAGAATGCAGAAGAAAAAATCCGC
    • length = 41bp
    • GC content = 48.8%
    • melting temp = 67.1 ºC
    • concentration =


P15: Reverse Primer for BioBrick prt B l.bulgaricus signal sequence

P15.png

    • sequence = CTGCAGCGGCCGCTACTAGTGGTAACCGGAGCCGTTTCTTG
    • length = 41bp
    • GC content = 61%
    • melting temp = 71.3 ºC
    • concentration =


P16: Forward Primer for BioBrick L. Bulgaricus lacS promoter

P16.jpg

    • sequence =


GAATTCGCGGCCGCTTCTAGAGAAGAGGCTATATCGCCATCATTAGCAGCTT

bold = biobrick prefix

    • length = 57 bp
    • GC content = 47.4%
    • melting temp = 68.7 ºC

P17: Reverse Primer for BioBrick L. Bulgaricus lacS promoter

P17.jpg

    • sequence =


CTGCAGCGGCCGCTACTAGTAGAAATTCTCCTTTAGGTGTGTTAACTTG

bold = biobrick suffix

    • length = 49 bp
    • GC content = 46.9%
    • melting temp = 67 ºC

P18: Forward Primer for BioBrick p1025

P18.png

    • sequence = GAATTCGCGGCCGCTTCTAGACAGCTGAAAACCGCTGACCTG
    • length = 42bp
    • GC content = 57.1%
    • melting temp = 70.2ºC

P19: Reverse Primer for BioBrick p1025

P19.png

    • sequence = CTGCAGCGGCCGCTACTAGTAACCAGAACGAAAGAGGTGG
    • length = 40 bp
    • GC content = 57.5%
    • melting temp = 69.2ºC

P20: Forward Primer for BioBrick GFP

P20.png

    • sequence = GAATTCGCGGCCGCTTCTAGACGTAAAGGAGAAGAACTTTTC
    • length = 42 bp
    • GC content = 47.6%
    • melting temp = 65.9ºC

P21: Reverse Primer for BIoBrick GFP

P21.png

    • sequence = CTGCAGCGGCCGCTACTAGTTTTGTATAGTTCATCCATGC
    • length = 40bp
    • GC content = 50%
    • melting temp = 66.5 ºC

P22: Forward Primer for BBa_I13521

P22.jpg

    • Will basically remove the promoter from this RFP device
    • sequence = gaattcgcggccgcttctagagtactagagaaagaggagaatac
    • length = 41 bp
    • GC content = 48.8%
    • melting temp = 65.9 C

P23: Reverse Primer for BBa_I13521

P23.jpg

    • sequence = ctgcagcggccgctactagtatataaacgcagaaaggcccac
    • length = 41 bp
    • GC content = 53.7%
    • melting temp = 68.9 C

P24: bbRBSfw: attach RBS upstream of p1025 part, with BB end

File:P24.jpg

    • sequence = GGAATTCGCGGCCGCTTCTAGAGTC...?
    • length = ? bp
    • GC content = ?%
    • melting temp = 69.4 C

P25: expfw: attach NdeI end to beginning of p1025 part

File:P25.jpg

    • sequence = GGAATTCCATATGCAGAAGAAAAA...?
    • length = ? bp
    • GC content = ?%
    • melting temp = 61.3 C

P26: exprev: attach XhoI end after p1025 part

File:P26.jpg

    • sequence = CCGCTCGAGTTATTAGTGGTGATG...?
    • length = ? bp
    • GC content = ?%
    • melting temp = 63.5 C

Plasmids

Include sequence, BioBrick #, functional features, digestion map.


PCR Products

1-1 GFP

GFP with linker @ 3' and [His, Terminator, Suffix] @ 5'

  • Template: GFP from Felix
  • Primers: 3 and 4

1-2 GFP

GFP with linker @ 3' and [His, Suffix] @ 5'

  • Template: GFP from Felix
  • Primers: 3 and 5

2-1 p1025

p1025 construct with [prefix, promoter, rbs] @ 3' and linker @ 5'

  • Template: p1025 construct
  • Primers: 1 and 2

gel image of parts

2-2 signal

L. bulgaricus signal peptide with Silver modified BioBricks prefix and suffix

  • Template: p1025 cnstruct
  • Primers: 14 and 15

2-3 Flag

Flag tag with Silver modified BioBricks prefix and suffix

  • Oligo annealing
  • Primers 6 and 7

2-4 HA

HA tag with Silver modified BioBricks prefix and suffix

  • Oligo annealing
  • Primers 8 and 9

2-5 His

His tag with Silver modified BioBricks prefix and suffix

  • Oligo annealing
  • Primers 10 and 11

2-6 Tev

Tev cleavage site with Silver modified BioBricks prefix and suffix

  • Oligo annealing
  • primers 12 and 13

Other

TEV Protease cut site

  • Amino Acid Sequence : Glu-Asn-Leu-Tyr-Phe-Gln-Gly (Cuts between Gln-Gly)
  • Base Pair Sequence: GAAAACCTGTACTTCCAGGGT


DNA sequence to synthesize - epitope/p1025/linker (6/17/08)

  • The signal peptide sequence (141 bp) can be found at [http://www.ncbi.nlm.nih.gov/sites/entrez?dispmax=1&db=nucleotide&doptcmdl=graph&term=104773257 the NCBI genome database]
  • 6/17, lengthened signal peptide so that it will cleave properly
  • silent mutations in linkers to reduce repetition and to ensure specificity of primers (ex. GGC/GGA/GGG instead of GGT coding for Gly)

P1025-epitope.png

sequence: ATGCAGAAGAAAAAATCCGCACGCCATTTGAACAAAGTGGCTGAATTAGCCGCAGCACTGCTCC TATCAGCGAGTCCACTGGCGGGAACTTTCCAGTCAGCCGCTTTTGTCCAAGCTGCCAGTCAAGA AACGgctccggttaccGACTACAAAGACGACGACGACAAAGGaGGTGGcCAGCTGAAAACCGCT GACCTGCCGGCTGGTCGTGACGAAACCACCTCTTTCGTTCTGGTTGGTGGaGGgTACCCGTACG ACGTTCCGGACTACGCTGGaGGtGGgTCTGGcGGtGGaTCaGGgGGtGGaTCgGAAAACCTGTA CTTCCAGGGTGGTGGaGGcTCcGGTGGcGGCagcGGcGGgGGCagc


L. bulgaricus lacS promoter to synthesize (7/11/08)

Placs.jpg

sequence:

GAATTCGCGGCCGCTTCTAGAGAAGAGGCTATATCGCCATCATTAGCAGCTTAATTGA ATATTTACTGGCTAAACTATTGAGTTTTCAAGGCTTCATAGTTCTTTTTGGTGTGGGA AGTTTAAATTACTAAAAATATTTTAGTAAAACATCTTGGTTTATTTAGTAAACAAGTC TATACTGTAATTATAAACAAGTTAACACACCTAAAGGAGAATTTCTACTAGTAGCGGC CGCTGCAG

Whole Sequence

CCGCTTCTAGAGTAATACGACTCACTATAGGGAATACAAG CTACTTGTTCTTTTTGCATACTAGAGATTAAAGAGGAGAA ATACTAGATGCAGAAGAAAAAATCCGCACGCCATTTGAAC AAAGTGGCTGAATTAGCCGCAGCACTGCTCCTATCAGCGA GTCCACTGGCGGGAACTTTCCAGTCAGCCGCTTTTGTCCA AGCTGCCAGTCAAGAAACGGCTCCGGTTACCGACTACAAA GACGACGACGACAAAGGaGGTGGcCAGCTGAAAACCGCTG ACCTGCCGGCTGGTCGTGACGAAACCACCTCTTTCGTTCT GGTTGGTGGaGGgTACCCGTACGACGTTCCGGACTACGCT GGaGGtGGgTCTGGcGGtGGaTCaGGgGGtGGaTCgGAAA ACCTGTACTTCCAGGGTGGTGGaGGcTCcGGTGGcGGCag cGGcGGgGGCagcATGCGTAAAGGAGAAGAACTTTTCACT GGAGTTGTCCCAATTCTTGTTGAATTAGATGGTGATGTTA ATGGGCACAAATTTTCTGTCAGTGGAGAGGGTGAAGGTGA TGCAACATACGGAAAACTTACCCTTAAATTTATTTGCACT ACTGGAAAACTACCTGTTCCATGGCCAACACTTGTCACTA CTTTCGGTTATGGTGTTCAATGCTTTGCGAGATACCCAGA TCATATGAAACAGCATGACTTTTTCAAGAGTGCCATGCCC GAAGGTTATGTACAGGAAAGAACTATATTTTTCAAAGATG ACGGGAACTACAAGACACGTGCTGAAGTCAAGTTTGAAGG TGATACCCTTGTTAATAGAATCGAGTTAAAAGGTATTGAT TTTAAAGAAGATGGAAACATTCTTGGACACAAATTGGAAT ACAACTATAACTCACACAATGTATACATCATGGCAGACAA ACAAAAGAATGGAATCAAAGTTAACTTCAAAATTAGACAC AACATTGAAGATGGAAGCGTTCAACTAGCAGACCATTATC AACAAAATACTCCAATTGGCGATGGCCCTGTCCTTTTACC AGACAACCATTACCTGTCCACACAATCTGCCCTTTCGAAA GATCCCAACGAAAAGAGAGACCACATGGTCCTTCTTGAGT TTGTAACAGCTGCTGGGATTACACATGGCATGGATGAACT ATACAAACATCATCACCATCACCACTAATAAAAATAATAA AAAAGCCGGATTAATAATCTGGCTTTTTATATTCTCTTAC TAGTAGCGGCCGCTGCAGGATTA

Wholesequence.png


Home The Team The Project Parts Submitted to the Registry Modeling Notebook
Retrieved from "http://2008.igem.org/Team:MIT/sequences"