Human TRIM54 ORF clone (NM_032546) (Cat. No.: V033509)
Basic Information
- Name:
- pLV-Tet-miniCMV-mCherry-Puro-TRIM54(human)-HA-GFP nanobody
- Accession ID:
- NM_032546.4
- Antibiotic Resistance:
- Ampicillin
- Length:
- 12357 bp
- Type:
- Protein expression, Tetracycline inducible
- Replication origin:
- ori
- Host:
- Mammalian cells, Lentivirus
- Selection Marker:
- Puro;mCherry
- Promoter:
- Tet-miniCMV
- 5' Primer:
- PFLAG-CMV-F
- Fusion Tag:
- HA-GFP nanobody
- Growth Strain(s):
- Stbl3
- Growth Temperature:
- 37℃
- Expression Method:
- Tetracycline inducible
- Gene Synonyms:
- MURF; MURF-3; muRF3; RNF30
- Transcript Definition:
- Homo sapiens tripartite motif containing 54 (TRIM54), transcript variant 1, mRNA
Cat. No.: V033509
pLV-Tet-miniCMV-mCherry-Puro-TRIM54(human)-HA-GFP nanobody
$
299.6
In stock, 1-2 weeks for quality controls
Buy one, get one free! (?)
Two tubes of transfection grade plasmid, each tube is about 100 µg (lyophilized).
Resources
Transcript ID
Fusion Tag
Selection Marker
Expression Method
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.
Human TRIM54 ORF clone (NM_032546) (Cat. No.: V033509) Sequence
LOCUS V033509 12357 bp DNA circular SYN 01-JAN-1980
DEFINITION synthetic circular DNA.
ACCESSION V033509
VERSION V033509
KEYWORDS .
SOURCE .
ORGANISM .
.
FEATURES Location/Qualifiers
misc_feature 25..142
/note="central polypurine tract and central termination
sequence of HIV-1"
/label="cPPT/CTS"
protein_bind 210..228
/bound_moiety="tetracycline repressor TetR"
/gene="tetO"
/note="bacterial operator O2 for the tetR and tetA genes"
/label="tet operator"
protein_bind 245..263
/bound_moiety="tetracycline repressor TetR"
/gene="tetO"
/note="bacterial operator O2 for the tetR and tetA genes"
/label="tet operator"
protein_bind 281..299
/bound_moiety="tetracycline repressor TetR"
/gene="tetO"
/note="bacterial operator O2 for the tetR and tetA genes"
/label="tet operator"
protein_bind 317..335
/bound_moiety="tetracycline repressor TetR"
/gene="tetO"
/note="bacterial operator O2 for the tetR and tetA genes"
/label="tet operator"
protein_bind 352..370
/bound_moiety="tetracycline repressor TetR"
/gene="tetO"
/note="bacterial operator O2 for the tetR and tetA genes"
/label="tet operator"
protein_bind 388..406
/bound_moiety="tetracycline repressor TetR"
/gene="tetO"
/note="bacterial operator O2 for the tetR and tetA genes"
/label="tet operator"
promoter 418..456
/note="human cytomegalovirus (CMV) immediate early
promoter"
/label="minimal CMV promoter"
promoter 524..542
/note="promoter for bacteriophage T7 RNA polymerase"
/label="T7 promoter"
CDS 614..1813
/label="TRIM54(NM_032546)"
/note="TRIM54(NM_032546)"
/gene="TRIM54"
CDS 1814..1840
/codon_start=1
/product="HA (human influenza hemagglutinin) epitope tag"
/transl_table=1
/translation="YPYDVPDYA"
/label="HA"
CDS 1886..2227
/codon_start=1
/product="GFP-binding fragment of a single-chain camelid
antibody (Rothbauer et al., 2008)"
/transl_table=1
/translation="VQLVESGGALVQPGGSLRLSCAASGFPVNRYSMRWYRQAPGKERE
WVAGMSSAGDRSSYEDSVKGRFTISRDDARNTVYLQMNSLKPEDTAVYYCNVNVGFEYW
GQGTQVTVSS"
/label="GFP nanobody"
promoter 2353..2852
/note="mouse phosphoglycerate kinase 1 promoter"
/label="PGK promoter"
CDS 2873..3580
/codon_start=1
/note="mammalian codon-optimized"
/product="monomeric derivative of DsRed fluorescent protein
(Shaner et al., 2004)"
/transl_table=1
/translation="MVSKGEEDNMAIIKEFMRFKVHMEGSVNGHEFEIEGEGEGRPYEG
TQTAKLKVTKGGPLPFAWDILSPQFMYGSKAYVKHPADIPDYLKLSFPEGFKWERVMNF
EDGGVVTVTQDSSLQDGEFIYKVKLRGTNFPSDGPVMQKKTMGWEASSERMYPEDGALK
GEIKQRLKLKDGGHYDAEVKTTYKAKKPVQLPGAYNVNIKLDITSHNEDYTIVEQYERA
EGRHSTGGMDELYK"
/label="mCherry"
CDS 3581..3637
/codon_start=1
/note="Eukaryotic ribosomes fail to insert a peptide bond
between the Gly and Pro residues, yielding separate
polypeptides."
/product="2A peptide from porcine teschovirus-1
polyprotein"
/transl_table=1
/translation="ATNFSLLKQAGDVEENPGP"
/label="P2A"
CDS 3638..4237
/codon_start=1
/gene="pac from Streptomyces alboniger"
/note="confers resistance to puromycin"
/product="puromycin N-acetyltransferase"
/transl_table=1
/translation="MTEYKPTVRLATRDDVPRAVRTLAAAFADYPATRHTVDPDRHIER
VTELQELFLTRVGLDIGKVWVADDGAAVAVWTTPESVEAGAVFAEIGPRMAELSGSRLA
AQQQMEGLLAPHRPKEPAWFLATVGVSPDHQGKGLGSAVVLPGVEAAERAGVPAFLETS
APRNLPFYERLGFTVTADVEVPEGPRTWCMTRKPGA*"
/label="PuroR"
misc_feature 4248..4836
/note="woodchuck hepatitis virus posttranscriptional
regulatory element"
/label="WPRE"
LTR 4899..5132
/note="self-inactivating 3' long terminal repeat (LTR)
from HIV-1"
/label="3' LTR (ΔU3)"
promoter complement(5157..5175)
/note="promoter for bacteriophage SP6 RNA polymerase"
/label="SP6 promoter"
promoter 5964..6068
/gene="bla"
/label="AmpR promoter"
CDS 6069..6929
/codon_start=1
/gene="bla"
/note="confers resistance to ampicillin, carbenicillin, and
related antibiotics"
/product="β-lactamase"
/transl_table=1
/translation="MSIQHFRVALIPFFAAFCLPVFA,HPETLVKVKDAEDQLGARVGY
IELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEY
SPVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDR
WEPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRS
ALPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGA
SLIKHW*"
/label="AmpR"
rep_origin 7100..7688
/direction=RIGHT
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
/label="ori"
promoter 7934..8263
/note="SV40 enhancer and early promoter"
/label="SV40 promoter"
intron 9397..9462
/note="SV40 (simian virus 40) small t antigen intron"
/label="small t intron"
CDS 9592..9612
/codon_start=1
/locus_tag=""
/note=""
/product="nuclear localization signal of SV40 (simian virus
40) large T antigen"
/protein_id=""
/transl_table=1
/translation="PKKKRKV"
/label="SV40 NLS"
polyA_signal 10037..10171
/note="SV40 polyadenylation signal"
/label="SV40 poly(A) signal"
LTR 10340..10973
/note="3' long terminal repeat (LTR) from HIV-1"
/label="3' LTR"
misc_feature 11020..11145
/note="packaging signal of human immunodeficiency virus
type 1"
/label="HIV-1 Ψ"
misc_feature 11637..11870
/note="The Rev response element (RRE) of HIV-1 allows for
Rev-dependent mRNA export from the nucleus to the
cytoplasm."
/label="RRE"
CDS 12055..12099
/codon_start=1
/note="recognized by the 2H10 single-chain llama nanobody"
/product="antigenic peptide corresponding to amino acids
655 to 669 of the HIV envelope protein gp41 (Lutje Hulsik
et al., 2013)"
/transl_table=1
/translation="KNEQELLELDKWASL"
/label="gp41 peptide"