2XMyc-LRRK2-D1994A vector (V014688)

Price Information

Cat No. Plasmid Name Availability Add to cart
V014688 2XMyc-LRRK2-D1994A 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:
2XMyc-LRRK2-D1994A
Antibiotic Resistance:
Kanamycin
Length:
11985 bp
Type:
Protein expression
Replication origin:
ori
Host:
Mammalian cells
Selection Marker:
Neo/G418
Promoter:
CMV
Growth Temperature:
37℃

2XMyc-LRRK2-D1994A vector Map

2XMyc-LRRK2-D1994A11985 bp50010001500200025003000350040004500500055006000650070007500800085009000950010000105001100011500CMV enhancerCMV promoterT3 promoterattB1Leucine-rich repeat serine/threonine-protein kinase 2attB2T7 promoterSV40 poly(A) signalf1 oriAmpR promoterSV40 promoterNeoR/KanRHSV TK poly(A) signalori

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.

2XMyc-LRRK2-D1994A vector Sequence

LOCUS       V014688                11985 bp    DNA     circular SYN 01-JAN-1980
DEFINITION  Exported.
ACCESSION   V014688
VERSION     V014688
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 11985)
  AUTHORS   .
  TITLE     Direct Submission
FEATURES             Location/Qualifiers
     source          1..11985
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     enhancer        81..384
                     /label="CMV enhancer"
                     /note="human cytomegalovirus immediate early enhancer"
     promoter        385..588
                     /label="CMV promoter"
                     /note="human cytomegalovirus (CMV) immediate early
                     promoter"
     promoter        634..652
                     /label="T3 promoter"
                     /note="promoter for bacteriophage T3 RNA polymerase"
     protein_bind    786..810
                     /label="attB1"
                     /note="recombination site for the Gateway(R) BP reaction"
     CDS             825..8405
                     /gene="LRRK2"
                     /label="Leucine-rich repeat serine/threonine-protein kinase
                     2"
                     /note="Leucine-rich repeat serine/threonine-protein kinase
                     2 from Homo sapiens. Accession#: Q5S007"
     protein_bind    complement(8427..8451)
                     /label="attB2"
                     /note="recombination site for the Gateway(R) BP reaction"
     promoter        complement(8501..8519)
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"
     polyA_signal    8793..8914
                     /label="SV40 poly(A) signal"
                     /note="SV40 polyadenylation signal"
     rep_origin      complement(8921..9376)
                     /direction=LEFT
                     /label="f1 ori"
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     promoter        9403..9505
                     /label="AmpR promoter"
     promoter        9509..9866
                     /label="SV40 promoter"
                     /note="SV40 enhancer and early promoter"
     CDS             9901..10692
                     /label="NeoR/KanR"
                     /note="aminoglycoside phosphotransferase"
     polyA_signal    10927..10974
                     /label="HSV TK poly(A) signal"
                     /note="herpes simplex virus thymidine kinase
                     polyadenylation signal (Cole and Stacy, 1985)"
     rep_origin      11303..11891
                     /direction=RIGHT
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"