Coding
mRFP1

Part:BBa_E2050:Experience

Designed by: ryu   Group: Antiquity   (2005-01-24)
Revision as of 13:56, 16 October 2010 by Slam (Talk | contribs) (→‎Applications of BBa_E2050)

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Applications of BBa_E2050

Part:BBa_E2050:Experience
Aberdeen iGEM 2010 Bio-brick Experience

The yeast mOrange open reading frame (Bio-brick E2050) was tested as part of a yeast expression construct, in which E2050 was translationally fused downstream of a tandem N-peptide open reading frame (Biobrick BBa_K385004). The gene fusion was placed under control of the GAL1 promoter (BioBrick K106699). The whole construct was cloned into a yeast shuttle vector and transformed into yeast. After growth of the transformant culture in medium containing galactose to induce the promoter, expression of mOrange was assessed using flow cytometry, (excitation wavelength 488nm, fluorescence wavelength 585nm). No mOrange fluorence was detectable by this method. However, a similar, related construct, in which the mOrange sequence was replaced by GFP, did express significant quantities of green fluorescent protein (see Aberdeen 2010 wiki for details ). This led us to conclude the mOrange sequence was non-functional in this particular expression construct.

User Reviews

UNIQ68944f5e4d1a737e-partinfo-00000001-QINU

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Slam

This part did not work in our GAL1 regulated construct.See above for more details.

Antiquity

This review comes from the old result system and indicates that this part did not work in some test.

UNIQ68944f5e4d1a737e-partinfo-00000004-QINU