pET28a-MH6-RspCas13d_RspCasWYL1 vector (V000654)

Price Information

Cat No. Plasmid Name Availability Add to cart
V000654 pET28a-MH6-RspCas13d_RspCasWYL1 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:
pET28a-MH6-RspCas13d_RspCasWYL1
Antibiotic Resistance:
Kanamycin
Length:
9416 bp
Type:
Bacterial Expression, CRISPR
Replication origin:
ori
Copy Number:
Low Copy
Promoter:
J23119
Cloning Method:
Restriction Enzyme
5' Primer:
ATGCTGATTCCGCCTAGCAC

pET28a-MH6-RspCas13d_RspCasWYL1 vector Vector Map

pET28a-MH6-RspCas13d_RspCasWYL19416 bp400800120016002000240028003200360040004400480052005600600064006800720076008000840088009200T7 promoterlac operatorlac promoterRBS6xHisRBS6xHisJ23119 promoterT7 terminatorf1 oriKanRoriL4440bompGEX 3'CAP binding sitelacIlacI promoterpBRrevBam

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.

pET28a-MH6-RspCas13d_RspCasWYL1 vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       pET28a-MH6-RspCa        9416 bp DNA     circular SYN 13-MAY-2021
DEFINITION  Expresses E. coli codon optimized RspCas13d and RspCasWYL1 in the 
            pET28a backbone..
ACCESSION   .
VERSION     .
KEYWORDS    pET28a-MH6-RspCas13d_RspCasWYL1
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 9416)
  AUTHORS   Yan WX, Chong S, Zhang H, Makarova KS, Koonin EV, Cheng DR, Scott DA
  TITLE     Cas13d Is a Compact RNA-Targeting Type VI CRISPR Effector Positively
            Modulated by a WYL-Domain-Containing Accessory Protein.
  JOURNAL   Mol Cell. 2018 Mar 9. pii: S1097-2765(18)30173-4. doi: 
            10.1016/j.molcel.2018.02.028.
  PUBMED    29551514
REFERENCE   2  (bases 1 to 9416)
  TITLE     Direct Submission
REFERENCE   3  (bases 1 to 9416)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: "Mol Cell. 
            2018 Mar 9. pii: S1097-2765(18)30173-4. doi: 
            10.1016/j.molcel.2018.02.028."
COMMENT     SGRef: number: 2; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..9416
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     promoter        1..19
                     /label=T7 promoter
                     /note="promoter for bacteriophage T7 RNA polymerase"
     protein_bind    20..44
                     /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        53..82
                     /label=lac promoter
                     /note="promoter for the E. coli lac operon"
     RBS             102..124
                     /label=RBS
                     /note="efficient ribosome binding site from bacteriophage
                     T7 gene 10 (Olins and Rangwala, 1989)"
     CDS             156..173
                     /label=6xHis
                     /note="6xHis affinity tag"
     RBS             2956..2978
                     /note="efficient ribosome binding site from bacteriophage
                     T7 gene 10 (Olins and Rangwala, 1989)"
     CDS             3010..3027
                     /label=6xHis
                     /note="6xHis affinity tag"
     promoter        4222..4256
                     /label=J23119 promoter
                     /note="bacterial promoter (Registry of Standard Biological
                     Parts BBa_J23119)"
     terminator      4365..4412
                     /label=T7 terminator
                     /note="transcription terminator for bacteriophage T7 RNA 
                     polymerase"
     rep_origin      4449..4904
                     /label=f1 ori
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     CDS             complement(4999..5811)
                     /label=KanR
                     /note="aminoglycoside phosphotransferase"
     rep_origin      5933..6521
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     primer_bind     6675..6692
                     /label=L4440
                     /note="L4440 vector, forward primer"
     misc_feature    complement(6707..6846)
                     /label=bom
                     /note="basis of mobility region from pBR322"
     primer_bind     6932..6954
                     /label=pGEX 3'
                     /note="pGEX vectors, reverse primer"
     CDS             complement(6951..7139)
                     /label=rop
                     /note="Rop protein, which maintains plasmids at low copy
                     number"
     protein_bind    complement(7914..7935)
                     /label=CAP binding site
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     CDS             complement(7951..9030)
                     /label=lacI
                     /note="lac repressor"
     promoter        complement(9031..9108)
                     /label=lacI promoter
     primer_bind     9314..9333
                     /label=pBRrevBam
                     /note="pBR322 vectors, tet region, downstream of BamHI,
                     reverse primer"