Gene:
Gene Symbol:
Gene Name:
Original Clone ID:
1322.1.12_GO.56038
Keyword:
None
Species:
Homo sapiens
Type:
cDNA
Vector Name:
pVP16
Format:
CLOSED
Source:
Center for Eukaryotic Structural Genomics
Description:
None
Comments:
His8-MBP fusion prtotein with TEV protease cleavage site is produced; after cleavage the protein obtained will be the translated CDS with the addition of SER at the N-term
Mutation / Discrepancy:
No / Yes
Publications:
None
Authors:
University of Wisconsin Madison
PSI
Center for Eukaryotic Structural Genomics
PSI
Center for Eukaryotic Structural Genomics
HsCD00085104
Price:
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AVAILABLE
No restriction
Special MTA: PSI
Special MTA: PSI
Insert sequence: 651nts
Open reading frame: 28 to 678
ACAAGTTTGTACAAAAAAGCAGGCTCCGAAAACCTGTACTTCCAGTCCGAGCTGAACTCC
CTGCTGATCCTGCTGGAGGCGGCCGAGTACCTGGAGCGCAGGGATCGAGAGGCCGAGCAC
GGCTACGCCTCGGTGCTGCCCTTCGACGGCGACTTCGCCAGGGAGAAAACAAAGGCGGCC
GGCCTGGTGCGCAAGGCCCCGAACAACAGGTCTTCACACAACGAGCTAGAAAAGCACAGA
CGAGCCAAACTCAGGCTGTACCTTGAGCAGCTCAAGCAACTGGTGCCCCTGGGCCCCGAC
AGTACCCGCCACACCACGCTGAGCCTCCTGAAGCGGGCCAAGGTGCACATCAAGAAACTG
GAGGAGCAGGACCGCCGGGCACTGAGCATCAAGGAGCAGCTGCAGCAGGAGCATCGTTTC
CTGAAGCGGCGCCTGGAGCAGCTGTCGGTGCAGAGCGTGGAGCGCGTGCGCACAGATAGC
ACGGGCTCTGCTGTCTCCACGGACGACTCAGAGCAAGAAGTGGACATAGAGGGCATGGAG
TTTGGCCCTGGTGAGCTGGACAGTGTTGGCAGCAGCAGTGACGCGGACGACCACTACAGC
CTGCAGAGTGGCACCGGCGGCGACAGTGGCTTCGGGCCCCACTGCCGGCGGCTGGGCCGC
CCCGCCCTCTCGTAGTAGGACCCAGCTTTCTTGTACAAAGTGGT
Protein sequence predicted based on nucleotide sequence
ENLYFQSELNSLLILLEAAEYLERRDREAEHGYASVLPFDGDFAREKTKAAGLVRKAPNN RSSHNELEKHRRAKLRLYLEQLKQLVPLGPDSTRHTTLSLLKRAKVHIKKLEEQDRRALS IKEQLQQEHRFLKRRLEQLSVQSVERVRTDSTGSAVSTDDSEQEVDIEGMEFGPGELDSV GSSSDADDHYSLQSGTGGDSGFGPHCRRLGRPALS**
Coding Sequence Details
Insert Sequence Verified?:
Y
Verification Method:
Sequence Verification
Reference Sequence Annotations:
Start on reference sequence
1
End on reference sequence
651
Mutations:
None
Discrepancy:
c276t,S92S;
5' Linker Sequence:
None
3' Linker Sequence:
None
Recommended Growth Condition:
Distributed in bacterial strain:
DH5-alpha T1 phage resistant
Antibiotic Selection:
Host Type:
bacterial
Marker:
ampicillin
Bacterial Selection Condition:
100 ug/mL ampicillin
Growth Condition:
Growth with the single antibiotic in LB at 37 degrees is recommended.
Comments:
Commonly used conditions for ampicillin resistant plasmid clones.
Protein Expression Results:
None
Recommended expression in:
Not Applicable
Vector Name:
pVP16
Synonyms:
''
Sequencing Primer:
Forward:
MBP Forward
Reverse:
pQE Reverse
Description:
Bacterial (E. coli) expression, adds N-terminal 8xHis and MBP, adds TEV site on 5p end of insert; ampicillin resistance in bacteria; recombinational cloning; Gateway cloning into this vector will remove the Gateway ccdB death casette.
Comments:
TEV protease cleavage site is "partial" and not functional. The TEV cleavage site must be added to the insert by PCR, which allows amino acids encoded by the attB1 site to be cut off after protein expression. Gateway cloning into this vector will remove the Gateway cassette
Size (bp):
7631
Parent Vector:
None
Properties:
Gateway, acceptor (destination), bacterial expression, recombinational cloning, with tag/fusion/marker
Author Name:
Center for Eukaryotic Structural Genomics
Publications:
PMID:
15750721
Title: Results from high-throughput DNA cloning of Arabidopsis thaliana target genes using site-specific recombination
Vector Map:
Vector Sequence:
Sequence:
Vector Features:
Type
Name
Description
Start
End
bacterial origin
ori
ColE1-type bacterial origin of replication
6471
5789
negative selection marker
ccdB
ccdB death cassette gene (lost in with-insert form)
2643
2852
promoter
T5
T5 promoter
5
54
recombination site
AttR1
AttR1 recombination site
1316
1440
recombination site
AttR2
AttR2 recombination site
3020
2896
repressor protein gene
LacI
LacI coding region
4132
5211
selectable marker
CmR
chloramphenicol resistance gene (CmR) (Lost in with-insert form)
1549
2205
selectable marker
AmpR
ampicillin resistance gene
7228
6569
tag
MBP
N-terminal MBP
148
1246
tag
His
N-terminal 8xHis tag
128
145
