Price Information
| Cat No. | Plasmid Name | Availability | Add to cart |
|---|---|---|---|
| V011275 | pCI-neo | 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:
- pCI-neo
- Antibiotic Resistance:
- Ampicillin
- Length:
- 5472 bp
- Type:
- Mammalian Expression Vectors
- Replication origin:
- ori
- Source/Author:
- Promega
- Selection Marker:
- Neomycin/G418(Geneticin)
- Copy Number:
- High copy number
- Promoter:
- SV40
pCI-neo 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.
pCI-neo vector Sequence
LOCUS pCI-neo. 5472 bp DNA circular SYN 01-JAN-1980
DEFINITION Mammalian cell expression vector with the CMV promoter and a
neomycin (G418) resistance marker.
ACCESSION .
VERSION .
KEYWORDS pCI-neo
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 5472)
AUTHORS Promega
TITLE Direct Submission
REFERENCE 2 (bases 1 to 5472)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"
FEATURES Location/Qualifiers
source 1..5472
/mol_type="other DNA"
/organism="synthetic DNA construct"
enhancer 139..517
/label=CMV enhancer
/note="human cytomegalovirus immediate early enhancer"
promoter 518..729
/label=CMV promoter
/note="human cytomegalovirus (CMV) immediate early
promoter"
intron 890..1022
/label=chimeric intron
/note="chimera between introns from human beta-globin and
immunoglobulin heavy chain genes"
promoter 1067..1085
/label=T7 promoter
/note="promoter for bacteriophage T7 RNA polymerase"
misc_feature 1085..1137
/label=MCS
/note="MCS"
/note="multiple cloning site"
promoter complement(1141..1158)
/note="T3 promoter"
/note="promoter for bacteriophage T3 RNA polymerase
(shorter by one base than the standard T3 promoter)"
polyA_signal complement(1176..1297)
/label=SV40 poly(A) signal
/note="SV40 polyadenylation signal"
rep_origin 1483..1938
/label=f1 ori
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"
promoter 2055..2412
/label=SV40 promoter
/note="SV40 enhancer and early promoter"
CDS 2463..3254
/label=NeoR/KanR
/note="aminoglycoside phosphotransferase"
polyA_signal 3321..3369
/label=poly(A) signal
/note="synthetic polyadenylation signal"
promoter 3675..3779
/label=AmpR promoter
CDS 3780..4637
/label=AmpR
/note="beta-lactamase"
rep_origin 4811..5399
/direction=RIGHT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"