Addgene - pET mOrange LIC cloning vector (u-mOrange) Plasmid Data

Plasmid 29770: pET mOrange LIC cloning vector (u-mOrange)

Gene/insert name:
None
Fusion protein or tag:
mOrange
Terminal:
C terminal on backbone
Vector backbone:
pET
(Search Vector Database)
Vector type:
Bacterial Expression
Backbone size (bp):
5472
Cloning site 5':
LIC site vuGFP
Site destroyed during cloning:
Yes
Cloning site 3':
LIC site vuGFP
Site destroyed during cloning:
Yes
5' sequencing primer:
T7 forward List of Sequencing Primers
3' sequencing primer:
mOrange reverse (5'gcaccttgaagcgcatgaact)
Bacterial resistance(s)
Ampicillin
Growth strain(s)
DH5alpha
Growth temperature (℃):
37
High or low copy:
Low Copy
Sequence: View sequences (2)
Map:
View map
Principal Investigator:
Scott Gradia
Terms and Licenses:
MTA
Clontech Limited Use Label License
EMD Millipore Limited Use Label License/Brookhaven pET Assurance Letter

Comments:

This plasmid is an empty vector. Your gene can be inserted with a LIC cloning protocol. This plasmid can be used as a single-expression vector, and it is also compatible with our 2-series polycistronic destination vectors (2D, 2E, and 2Z), if co-expression with other genes is desired.

mOrange has a excitation max of 548 nm and an emission max of 562 nm.

To clone into this vector, add LIC tags to the 5' end of your PCR primers.

Forward - 5' TTTAAGAAGGAGATATAGATC3'

Reverse - 5' GTTGGAGGATGAGAGGATCCC 3'

Do NOT include a stop codon with your reverse primer.

Linearize the plasmid with EcoRV, then gel purify.

When digesting the DNA with T4 polymerase, use dGTP for the insert and dCTP for your linearized vector.

More information on this vector can be found through http://qb3.berkeley.edu/qb3/macrolab/

Addgene has sequenced a portion of this plasmid for verification. Click here for the sequencing result.

Please acknowledge the principal investigator and cite this article if you use this plasmid in a publication. Also, please include the text "Addgene plasmid 29770" in your Materials and Methods section.