Price Information
| Cat No. | Plasmid Name | Availability | Add to cart |
|---|---|---|---|
| V006905 | pF151 pcDNA3.1(+)SOD1WT | In stock, 1 week for quality controls |
Buy one, get one free! |
Two tubes of lyophilized plasmid will be delivered, each tube is about 5µg.
Basic Vector Information
- Vector Name:
- pF151 pcDNA3.1(+)SOD1WT
- Antibiotic Resistance:
- Ampicillin
- Length:
- 5872 bp
- Type:
- Mammalian Expression
- Replication origin:
- ori
- Selection Marker:
- Neomycin (select with G418)
- Copy Number:
- High Copy
- Cloning Method:
- Restriction Enzyme
- 5' Primer:
- CMV-F
- 3' Primer:
- BGH-rev
pF151 pcDNA3.1(+)SOD1WT vector Map
Plasmid Protocol
1. Centrifuge at 5,000×g for 5 min.
2. Carefully open the tube and add 20 μl of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin to concentrate the liquid at the bottom. Speed is less than 5000×g.
5. Store the plasmid at -20 ℃.
6. The concentration of plasmid re-measurement sometimes differs from the nominal value, which may be due to the position of the lyophilized plasmid in the tube, the efficiency of the re-dissolution, the measurement bias, and adsorption on the wall of the tube, therefore, it is recommended to transform and extract the plasmid before using it
General Plasmid Transform Protocol
1. Take one 100μl of the competent cells and thaw it on ice for 10min, add 2μl of plasmid, then ice bath for 30min, then heat-shock it at 42℃ for 60s, do not stir, and then ice bath for 2min.
2. Add 900μl of LB liquid medium without antibiotics, and incubate at 37℃ for 45min (30℃ for 1-1.5 hours) with 180rpm shaking.
3. Centrifuge at 6000rpm for 5min, leave only 100μl of supernatant to resuspend the bacterial precipitate and spread it onto the target plasmid-resistant LB plate.
4. Invert the plate and incubate at 37℃ for 14h, or at 30℃ for 20h.
5. Pick a single colony into LB liquid medium, add the corresponding antibiotics, incubate at 220rpm for 14h, and extract the plasmid according to the experimental needs and the instructions of the plasmid extraction kit.
pF151 pcDNA3.1(+)SOD1WT vector Sequence
LOCUS V006905 5872 bp DNA circular SYN 13-MAY-2021
DEFINITION Exported.
ACCESSION V006905
VERSION V006905
KEYWORDS pF151 pcDNA3.1(+)SOD1WT
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 5872)
AUTHORS Stevens JC, Chia R, Hendriks WT, Bros-Facer V, van Minnen J, Martin
JE, Jackson GS, Greensmith L, Schiavo G, Fisher EM
TITLE Modification of superoxide dismutase 1 (SOD1) properties by a GFP
tag--implications for research into amyotrophic lateral sclerosis
(ALS).
JOURNAL PLoS One. 2010 . 5(3):e9541.
PUBMED 20221404
REFERENCE 2 (bases 1 to 5872)
TITLE Direct Submission
REFERENCE 3 (bases 1 to 5872)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "PLoS One.
2010 . 5(3):e9541."
SGRef: number: 2; type: "Journal Article"
FEATURES Location/Qualifiers
source 1..5872
/mol_type="other DNA"
/organism="synthetic DNA construct"
enhancer 14..393
/label="CMV enhancer"
/note="human cytomegalovirus immediate early enhancer"
promoter 394..597
/label="CMV promoter"
/note="human cytomegalovirus (CMV) immediate early
promoter"
promoter 642..660
/label="T7 promoter"
/note="promoter for bacteriophage T7 RNA polymerase"
CDS 738..1199
/gene="SOD1"
/label="Superoxide dismutase [Cu-Zn]"
/note="Superoxide dismutase [Cu-Zn] from Pan troglodytes.
Accession#: P60052"
polyA_signal 1248..1472
/label="bGH poly(A) signal"
/note="bovine growth hormone polyadenylation signal"
rep_origin 1518..1946
/label="f1 ori"
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"
promoter 1960..2289
/label="SV40 promoter"
/note="SV40 enhancer and early promoter"
CDS 2356..3147
/label="NeoR/KanR"
/note="aminoglycoside phosphotransferase"
polyA_signal 3324..3457
/label="SV40 poly(A) signal"
/note="SV40 polyadenylation signal"
primer_bind complement(3494..3510)
/label="M13 rev"
/note="common sequencing primer, one of multiple similar
variants"
protein_bind complement(3518..3534)
/label="lac operator"
/note="The lac repressor binds to the lac operator to
inhibit transcription in E. coli. This inhibition can be
relieved by adding lactose or
isopropyl-beta-D-thiogalactopyranoside (IPTG)."
promoter complement(3542..3572)
/label="lac promoter"
/note="promoter for the E. coli lac operon"
protein_bind complement(3587..3608)
/label="CAP binding site"
/note="CAP binding activates transcription in the presence
of cAMP."
primer_bind complement(3725..3742)
/label="L4440"
/note="L4440 vector, forward primer"
rep_origin complement(3896..4484)
/direction=LEFT
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
CDS complement(4658..5515)
/label="AmpR"
/note="beta-lactamase"
promoter complement(5516..5620)
/label="AmpR promoter"
primer_bind complement(5695..5714)
/label="pRS-marker"
/note="pRS vectors, use to sequence yeast selectable
marker"