Difference between revisions of "Part:BBa K3740018"

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<h3>Usage</h3>
 
<h3>Usage</h3>
 
<p>Constructed J23100-RBS004-sfGFP-rrn B T1 (BBa_K3740059) was transformed into E. coli DH5α. we quantified the fluorescence intensity when the optical absorbance of bacterial culture at 600nm was around 0.2</p>
 
<p>Constructed J23100-RBS004-sfGFP-rrn B T1 (BBa_K3740059) was transformed into E. coli DH5α. we quantified the fluorescence intensity when the optical absorbance of bacterial culture at 600nm was around 0.2</p>
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<br>
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<h3>Characterization</h3>
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<p>The average fluorescence intensity of sfGFP induced by RBS004 (BBa_K3740018), was less than 3% of B0034 (BBa_B0034). </p>
 +
[[File:szpt9.png|300px|thumb|center]]

Revision as of 06:11, 10 October 2021


RBS004

Description

Responsible for the recruitment of a ribosome during the initiation of translation

Usage and Biology

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]



2021 SZPT-China

Biology

Mutagenesis at specific position of RBS (BBa_B0034) was achieved RBS004 (BBa_K3740018) using random primers and PCR, and the constructed plasmid J23100-RBS004-sfGFP-rrn B T1 (BBa_K3740059). Compare the fluorescence intensity of sfGFP induced by J23100-B0034-sfGFP-rrn B T1 (BBa_K3740058)


Usage

Constructed J23100-RBS004-sfGFP-rrn B T1 (BBa_K3740059) was transformed into E. coli DH5α. we quantified the fluorescence intensity when the optical absorbance of bacterial culture at 600nm was around 0.2


Characterization

The average fluorescence intensity of sfGFP induced by RBS004 (BBa_K3740018), was less than 3% of B0034 (BBa_B0034).

Szpt9.png