pPICZB vector (V012801)

Price Information

Cat No. Plasmid Name Availability Add to cart
V012801 pPICZB In stock, 1 week for quality controls

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Two tubes of lyophilized plasmid will be delivered, each tube is about 5µg.

Basic Vector Information

Vector Name:
pPICZB
Antibiotic Resistance:
Bleomycin
Length:
3328 bp
Type:
Yeast Plasmids
Replication origin:
ori
Source/Author:
Invitrogen
Selection Marker:
Zeocin
Copy Number:
High copy number
Promoter:
AOX1
Cloning Method:
Enzyme Cut
5' Primer:
5´ AOX1:5´-GACTGGTTCCAATTGACAAGC-3´
3' Primer:
3´ AOX1:5´-GCAAATGGCATTCTGACATCC-3´
Fusion Tag:
C-myc, C-His6
Expression Method:
Constiutive, Stable / Transient

pPICZB vector Vector Map

pPICZB3328 bp6001200180024003000AOX1 promoterMyc6xHisAOX1 terminatorTEF1 promoterEM7 promoterBleoRCYC1 terminatorori

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.

pPICZB vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       pPICZB.        3328 bp DNA     circular SYN 31-MAY-2022
DEFINITION  synthetic circular DNA.
ACCESSION   .
VERSION     .
KEYWORDS    pPICZB
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 3328)
  TITLE     Direct Submission
FEATURES             Location/Qualifiers
     source          1..3328
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     promoter        2..940
                     /label=AOX1 promoter
                     /note="inducible promoter, regulated by methanol"
     CDS             1010..1039
                     /label=Myc
                     /note="Myc (human c-Myc proto-oncogene) epitope tag"
     CDS             1055..1072
                     /label=6xHis
                     /note="6xHis affinity tag"
     terminator      1152..1398
                     /label=AOX1 terminator
                     /note="transcription terminator for AOX1"
     promoter        1413..1824
                     /label=TEF1 promoter
                     /note="promoter for EF-1-alpha"
     promoter        1832..1879
                     /label=EM7 promoter
                     /note="synthetic bacterial promoter"
     CDS             1898..2269
                     /label=BleoR
                     /note="antibiotic-binding protein"
     terminator      2338..2585
                     /label=CYC1 terminator
                     /note="transcription terminator for CYC1"
     rep_origin      complement(2660..3248)
                     /direction=LEFT
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"