pcDNA5-Flag-BRD4-WT vector (V000591)

Price Information

Cat No. Plasmid Name Availability Add to cart
V000591 pcDNA5-Flag-BRD4-WT 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:
pcDNA5-Flag-BRD4-WT
Antibiotic Resistance:
Ampicillin
Length:
9333 bp
Type:
Mammalian Expression
Replication origin:
ori
Selection Marker:
Hygromycin

pcDNA5-Flag-BRD4-WT vector Map

pcDNA5-Flag-BRD4-WT9333 bp400800120016002000240028003200360040004400480052005600600064006800720076008000840088009200pRS-markerCMV enhancerCMV promotertet operatortet operatorLNCXFLAGBromodomain-containing protein 4bGH poly(A) signalF1ori-RFRTHygRSV40 poly(A) signalM13 revlac operatorlac promoterCAP binding siteL4440oriAmpRAmpR 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.

pcDNA5-Flag-BRD4-WT vector Sequence

LOCUS       V000591                 9333 bp    DNA     circular SYN 13-MAY-2021
DEFINITION  Exported.
ACCESSION   V000591
VERSION     V000591
KEYWORDS    pcDNA5-Flag-BRD4-WT
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 9333)
  AUTHORS   Shu S, Lin CY, He HH, Witwicki RM, Tabassum DP, Roberts JM,
            Janiszewska M, Huh SJ, Liang Y, Ryan J, Doherty E, Mohammed H, Guo
            H, Stover DG, Ekram MB, Peluffo G, Brown J, D'Santos C, Krop IE,
            Dillon D, McKeown M, Ott C, Qi J, Ni M, Rao PK, Duarte M, Wu SY,
            Chiang CM, Anders L, Young RA, Winer EP, Letai A, Barry WT, Carroll
            JS, Long HW, Brown M, Liu XS, Meyer CA, Bradner JE, Polyak K
  TITLE     Response and resistance to BET bromodomain inhibitors in
            triple-negative breast cancer.
  JOURNAL   Nature. 2016 Jan 21;529(7586):413-7. doi: 10.1038/nature16508. Epub
            2016 Jan 6.
   PUBMED   26735014
REFERENCE   2  (bases 1 to 9333)
  TITLE     Direct Submission
REFERENCE   3  (bases 1 to 9333)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; doi:
            "10.1038/nature16508"; journalName: "Nature"; date: "2016-01-21-
            21"; volume: "529"; issue: "7586"; pages: "413-7"
            SGRef: number: 2; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..9333
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     primer_bind     complement(23..42)
                     /label="pRS-marker"
                     /note="pRS vectors, use to sequence yeast selectable
                     marker"
     enhancer        214..593
                     /label="CMV enhancer"
                     /note="human cytomegalovirus immediate early enhancer"
     promoter        594..797
                     /label="CMV promoter"
                     /note="human cytomegalovirus (CMV) immediate early
                     promoter"
     protein_bind    799..817
                     /label="tet operator"
                     /note="bacterial operator O2 for the tetR and tetA genes"
     protein_bind    820..838
                     /gene="tetO"
                     /label="tet operator"
                     /bound_moiety="tetracycline repressor TetR"
                     /note="bacterial operator O2 for the tetR and tetA genes"
     primer_bind     848..872
                     /label="LNCX"
                     /note="Human CMV promoter, forward primer"
     CDS             971..994
                     /label="FLAG"
                     /note="FLAG(R) epitope tag, followed by an enterokinase
                     cleavage site"
     CDS             1001..5086
                     /gene="BRD4"
                     /label="Bromodomain-containing protein 4"
                     /note="Bromodomain-containing protein 4 from Homo sapiens.
                     Accession#: O60885"
     polyA_signal    5270..5494
                     /label="bGH poly(A) signal"
                     /note="bovine growth hormone polyadenylation signal"
     primer_bind     complement(5627..5646)
                     /label="F1ori-R"
                     /note="F1 origin, reverse primer"
     protein_bind    5778..5825
                     /label="FRT"
                     /note="FLP-mediated recombination occurs in the 8-bp core
                     sequence TCTAGAAA (Turan and Bode, 2011)."
     CDS             5833..6852
                     /label="HygR"
                     /note="aminoglycoside phosphotransferase from E. coli"
     polyA_signal    6985..7118
                     /label="SV40 poly(A) signal"
                     /note="SV40 polyadenylation signal"
     primer_bind     complement(7155..7171)
                     /label="M13 rev"
                     /note="common sequencing primer, one of multiple similar
                     variants"
     protein_bind    complement(7179..7195)
                     /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(7203..7233)
                     /label="lac promoter"
                     /note="promoter for the E. coli lac operon"
     protein_bind    complement(7248..7269)
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     primer_bind     complement(7386..7403)
                     /label="L4440"
                     /note="L4440 vector, forward primer"
     rep_origin      complement(7557..8145)
                     /direction=LEFT
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     CDS             complement(8319..9176)
                     /label="AmpR"
                     /note="beta-lactamase"
     promoter        complement(9177..9281)
                     /label="AmpR promoter"