BBa_K187229

BBa_K187229 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_K187229
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Julia Pon
Date created: 2009-10-18 11:00:00
Date modified: 2015-05-08 01:11:10

trxB ORF reverse primer



Types
DnaRegion

Roles
primer

Primer

Sequences BBa_K187229_sequence (Version 1)

Description

BBa_K187229

Notes

This primer produced a product of the predicted size using the following reaction conditions:

Water: 17.05uL
10x pfu buffer: 2.5uL
dNTPs (2mM): 2.5uL
DMSO: 1.2uL
MG1655 Genomic DNA: 0.5uL
Forward primer (10uM): 0.5uL
Reverse primer (10uM): 0.5uL
Pfu polymerase: 0.25uL

Total reaction volume: 25uL

Thermocycling conditions:
95oC, 3min
95oC, 30s
56oC, 30s
72oC, 3min
29 cycles to step 2
72oC 2min
All Biobytes essential gene primers were produced using Vector NTI. Each primer's thermodynamic properties were examined using Vector NTI's hairpin and dimerzation programs. Primers were optimized to fit as many of the following criteria as possible:
??? Find the shortest possible sequence, reducing the cost to produce the primer.
??? Produce the highest score value possible.
??? Produce the closest Tm's possible
??? Produce hairpins with dG values >-5
??? Produce dimers with dG values >-10
The following are Vector NTI statistics for this primer:
dG Dimer (kcal/mol): -2.3
dG Hairpin (kcal/mol): -0.7

Source

Oligonucleotides were synthesized. Primers were tested using MG1655 E.coli genomic DNA as template

igem#experience
Works
 
igem#sampleStatus
Not in stock
igem#status
Unavailable
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_K187229/1