Melbourne/Plan:Gas vesicles

From 2007.igem.org

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Steps:
Steps:
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#      Usefull links [[Melbourne/primary Restriction enzymes|(restriction enzymes)]][[Melbourne/Software|(Software)]]
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#      Usefull links [[Melbourne/primary Restriction enzymes|(restriction enzymes)]][[Melbourne/Software|(Software)]][[http://www.openwetware.org/wiki/Designing_primers|<open wetware primer design>]] [[http://www.mcb.uct.ac.za/pcroptim.htm|<more primer design>]]
#      Sequences:
#      Sequences:
##      Ncbi genebank AF053765  [[Melbourne/AF053765-pNL26|(pNL26 7371bp)]]  [[Melbourne/AF053765-pNL29|(pNL29 6036bp)]] [http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=nuccore&id=3089519| (original source)] [[Melbourne/AF053765FASTA| (FASTA seq.)]]
##      Ncbi genebank AF053765  [[Melbourne/AF053765-pNL26|(pNL26 7371bp)]]  [[Melbourne/AF053765-pNL29|(pNL29 6036bp)]] [http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=nuccore&id=3089519| (original source)] [[Melbourne/AF053765FASTA| (FASTA seq.)]]

Revision as of 02:18, 16 July 2007

Steps:

  1. Usefull links (restriction enzymes)(Software)[<open wetware primer design>] [<more primer design>]
  2. Sequences:
    1. Ncbi genebank AF053765 (pNL26 7371bp) (pNL29 6036bp) (original source) (FASTA seq.)
    2. pBluescriptIIKS+ (stratagene) (sequence) (restriction map) (map) (Manual)
    3. pNL26 Plasmid with insert: (seq 10318bp) (res map) (digests)
      1. pNL26 insert PstI--HindIII:(pNL26 7371bp)
    4. pNL29 Plasmid with insert: (seq 8983bp) (res map) (digests)
      1. pNL29 insert PstI--HindIII:(pNL29 6036bp)
  1. Recovery of genes: (2 days)
    1. Recover the plasmid from paper provided into solution.(method)
    2. Transform E.Coli strain DH5alpha. Screen with Amp 100ug/ml (as per ref.)(electroporation & heatshock)
    3. pick 3 colonies of each
    4. Overnight Culture x9(6 above and 3 form agar block provided)
    5. Miniprep
    6. Produce glycerol stocks
    7. Confirm presence in recovered sample using digest.(HindIII)
    8. ->Established Supply of Plasmid
  1. Induce translation overnight 37deg with IPTG in 100ml plates (method)(2days)
    1. Confirm transcription RT-PRC,
    2. Confirm translation (buoyant phenotype method).
    3. Confirm translation (Namarski optics (direct interferance contrast microscopy method).
  1. Removal of four biobrick like restriction sites all in GvpL.
    1. EcoRI [GAATTC] in gvpL (2858)
    2. PstI [CTGCAG] in gvpL x 3 (2522,2900,3005)
    3. XbaI [TCTAGA] (not present)
    4. SpeI [ACTAGT] (not present)
  1. Insertion of biobrick required restriction sites by PCR primer modification.(method)
    1. Design of primers
    2. Primer generation
    3. Plasmid extraction from culture
    4. PCR
    5. Restriction EcoR1 & Spe1
    6. Gel separation
    7. Restriction of standard Library death plasmid EcoR1,Spe1.
    8. Ligation.
    9. Transform host with regulated POPS output
    10. Confirm dna, rna , protein (as for A)