pBABEpuro U3-hTR-500 vector (V007209)

Price Information

Cat No. Plasmid Name Availability Add to cart
V007209 pBABEpuro U3-hTR-500 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:
pBABEpuro U3-hTR-500
Antibiotic Resistance:
Ampicillin
Length:
6891 bp
Type:
Mammalian Expression, Retroviral
Replication origin:
ori
Selection Marker:
Puromycin
Cloning Method:
Restriction Enzyme

pBABEpuro U3-hTR-500 vector Vector Map

pBABEpuro U3-hTR-5006891 bp3006009001200150018002100240027003000330036003900420045004800510054005700600063006600LTRMMLV Psigag (truncated)SV40 promoterPuroRSK primerT7 promoterM13 fwdF1ori-Rlong terminal repeat from Moloney murine leukemiavirusL4440oriAmpRAmpR promoter

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.

pBABEpuro U3-hTR-500 vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       pBABEpuro_U3-hTR        6891 bp DNA     circular SYN 29-JUL-2021
DEFINITION  synthetic circular DNA.
ACCESSION   .
VERSION     .
KEYWORDS    pBABEpuro U3-hTR-500
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 6891)
  AUTHORS   Wong JM, Collins K
  TITLE     Telomerase RNA level limits telomere maintenance in X-linked 
            dyskeratosis congenita.
  JOURNAL   Genes Dev. 2006 Oct 15. 20(20):2848-58.
  PUBMED    17015423
REFERENCE   2  (bases 1 to 6891)
  TITLE     Direct Submission
REFERENCE   3  (bases 1 to 6891)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: "Genes Dev. 
            2006 Oct 15. 20(20):2848-58."
COMMENT     SGRef: number: 2; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..6891
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     LTR             1..470
                     /label=LTR
                     /note="long terminal repeat from Moloney murine leukemia
                     virus"
     misc_feature    535..734
                     /label=MMLV Psi
                     /note="packaging signal of Moloney murine leukemia virus
                     (MMLV)"
     CDS             935..1351
                     /label=gag (truncated)
                     /note="truncated Moloney murine leukemia virus (MMLV) gag
                     gene lacking the start codon"
     promoter        1414..1743
                     /label=SV40 promoter
                     /note="SV40 enhancer and early promoter"
     CDS             1753..2349
                     /label=PuroR
                     /note="puromycin N-acetyltransferase"
     primer_bind     complement(3825..3841)
                     /label=SK primer
                     /note="common sequencing primer, one of multiple similar 
                     variants"
     promoter        complement(3874..3892)
                     /label=T7 promoter
                     /note="promoter for bacteriophage T7 RNA polymerase"
     primer_bind     complement(3899..3915)
                     /label=M13 fwd
                     /note="common sequencing primer, one of multiple similar 
                     variants"
     primer_bind     complement(4144..4163)
                     /label=F1ori-R
                     /note="F1 origin, reverse primer"
     LTR             4378..4847
                     /note="long terminal repeat from Moloney murine leukemia
                     virus"
     primer_bind     complement(4977..4994)
                     /label=L4440
                     /note="L4440 vector, forward primer"
     rep_origin      complement(5148..5736)
                     /direction=LEFT
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     CDS             complement(5899..6756)
                     /label=AmpR
                     /note="beta-lactamase"
     promoter        complement(6757..6861)
                     /label=AmpR promoter