pUC35s-RAT5-a-mCherry vector (V012971)

Price Information

Cat No. Plasmid Name Availability Add to cart
V012971 pUC35s-RAT5-a-mCherry 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:
pUC35s-RAT5-a-mCherry
Antibiotic Resistance:
Ampicillin
Length:
4890 bp
Type:
Protein expression
Replication origin:
ori
Host:
Plants
Promoter:
CaMV35S(long)
Growth Strain(s):
DH5a
Growth Temperature:
37℃

pUC35s-RAT5-a-mCherry vector Map

pUC35s-RAT5-a-mCherry4890 bp6001200180024003000360042004800M13 revCaMV 35S promoterHistone H2A.6mCherryNOS terminatorM13 fwdAmpR promoterAmpRoriCAP binding sitelac promoterlac operator

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.

pUC35s-RAT5-a-mCherry vector Sequence

LOCUS       V012971                 4890 bp    DNA     circular SYN 01-JAN-1980
DEFINITION  Exported.
ACCESSION   V012971
VERSION     V012971
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 4890)
  AUTHORS   .
  TITLE     Direct Submission
FEATURES             Location/Qualifiers
     source          1..4890
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     primer_bind     1..17
                     /label="M13 rev"
                     /note="common sequencing primer, one of multiple similar
                     variants"
     promoter        541..886
                     /label="CaMV 35S promoter"
                     /note="strong constitutive promoter from cauliflower mosaic
                     virus"
     CDS             901..1290
                     /gene="RAT5"
                     /label="Histone H2A.6"
                     /note="Histone H2A.6 from Arabidopsis thaliana. Accession#:
                     Q9LD28"
     CDS             1303..2010
                     /label="mCherry"
                     /note="monomeric derivative of DsRed fluorescent protein
                     (Shaner et al., 2004)"
     terminator      2030..2282
                     /label="NOS terminator"
                     /note="nopaline synthase terminator and poly(A) signal"
     primer_bind     complement(2291..2307)
                     /label="M13 fwd"
                     /note="common sequencing primer, one of multiple similar
                     variants"
     promoter        2781..2885
                     /label="AmpR promoter"
     CDS             2886..3743
                     /label="AmpR"
                     /note="beta-lactamase"
     rep_origin      3917..4505
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     protein_bind    4793..4814
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     promoter        4829..4859
                     /label="lac promoter"
                     /note="promoter for the E. coli lac operon"
     protein_bind    4867..4883
                     /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)."