pCMV6-AC-Myc-DDK-IRES-GFP-Puro Mammalian Expression Vector

SKU
PS100059
pCMV6-AC-IRES-GFP-Puro, mammalian vector with IRES-GFP and puro selection, 10ug
  $670.00
In Stock*
Specifications
Specifications
Product Data
C-Tag Myc-DDK
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Puromycin
Expression Promoter CMV
Features
  • ORFs cloned in this vector will be expressed as a tagged protein with a C-terminal Myc-DDK tag.
  • TurboGFP is expressed from IRES as part of the bicistronic transcript.
  • The mammalian selection marker for this vector is puromycin
  • Such clones are the best for detection and purification of the transgene expression using an anti-Myc and anti-DDK antibody.
  • V2_F Primer can be used to sequence the target sequence after cloning.
  • IRES100 Primer can be used to sequence the target sequence after cloning.
Download Vector Sequence
Schematic of the multiple cloning sites
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Documents
Resources

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Trafficking of the glutamate transporter is impaired in LRRK2-related Parkinson's disease
Iovino, Giusti, Pischedda et al
Acta Neuropathol (2022) 144 (1), 81-106 DOI: 10.1007/s00401-022-02437-0
Cited by 60
AI Summary: In this study, the pCMV6-mGLT-1 (Myc-DDK-tagged) plasmid (Cat. MR226166) from OriGene was used to express the mouse glutamate transporter GLT-1, enabling investigation of how LRRK2 G2019S impairs glutamate transporter trafficking in Parkinson's disease.
Snippet: 2019S variant were described in [3]. The pCMV6-mGLT-1 (Myc-DDK-tagged) plasmid encoding the mouse glial high-affinity glutamate transporter member 2 (Slc1a2), transcript variant 1, was purchased from OriGene Technologies Inc (Cat. MR226166). For the pEGFP-rat Glt1 plasmid, the 99–1820 bp fragment of the Rat Glt-1 plasmid (GenBankTM accession number X67857.1) was subcloned between the EcoRI and
FigureFigureFigure
The impact of CCR8+ regulatory T cells on cytotoxic T cell function in human lung cancer
Haruna, Ueyama, Yamamoto et al
Sci Rep (2022) 12 (1), 5377 DOI: 10.1038/s41598-022-09458-5
Cited by 68
AI Summary: OriGene’s pCMV6-AC-Myc-DDK-IRES-GFP-Puro Mammalian Expression Vector was used to generate H-2Kb-expressing LLC cells, enabling functional studies of immune cell interactions in the lung cancer model described in this paper.
Snippet: s 100%. Establishment of H-2Kb-expressing LLC cells The H-2Kb cDNA was synthesized from mRNA of C57BL/6 mouse spleen and inserted into the pCMV6-AC-Myc-DDK-IRES-GFP-Puro Mammalian Expression Vector (ORIGENE, USA, Rockville, MD, USA). LLC cells, purchased from American Type Culture Collection, were transfected with pCMV6-AC-Myc-DDK-IRES-GFP-Puro-H-2Kb by Lipofectamine 3000 Reagent (Thermo Fisher S...
FigureFigureFigure
Cytoplasmic ends of tetraspanin 7 harbour epitopes recognised by autoantibodies in type 1 diabetes
Eugster, Kraus, Lidzba et al
Diabetologia (2019)
AI Summary: OriGene’s pCMV6-AC-IRES-GFP-Puro vector was used to clone and express various tetraspanin 7 protein fragments, enabling the identification of key autoantibody-binding epitopes in type 1 diabetes.
Snippet: E2-TM4-C3 (AA 113-249), TM4-C3 (AA 214-249) and C3 (AA 235-249) tetraspanin 7 fragments NH2-terminally fused to NanoLuc were constructed by PCR amplification from full-length tetraspanin 7 [7] and cloning into pCMV6-AC-IRES-GFP-Puro (Origene, Rockville
Novel minor HLA DR associated antigens in type 1 diabetes
Müller, Telieps, Eugster et al
Clin. Immunol. (2018) 194, 87-91 DOI: 10.1016/j.clim.2018.07.001
AI Summary: OriGene’s pCMV6-AC-IRES-GFP-Puro vectors were used to clone and express full-length NUP50 and MTIF3 for the luciferase immunoprecipitation assays in this study.
Snippet: 2.2. Cloning and expression of antigens. cDNA from human peripheral mononuclear cells was used to clone full length NUP50 and MTIF3 into pCMV6-AC-IRES- GFP-Puro (Origene, MD, USA) containing NanoLuc Luciferase
Estrogen-induced transcription factor EGR1 regulates c-Kit transcription in the mouse uterus to maintain uterine receptivity for embryo implantation
Park, Kim, Kim et al
Mol. Cell. Endocrinol. (2017)
AI Summary: OriGene’s pCMV6-AC-IRES-GFP-Puro vector was used to clone and tag human EGR1 with Myc and FLAG, enabling the study of EGR1’s role in regulating c-Kit transcription in the mouse uterus.
Snippet: …Human EGR1 was amplified and cloned into the pCMV6-AC-IRES-GFP-Puro vector to tag EGR1 with Myc and FLAG (Origene Technologies, Rockville, MD, USA). 293T ...;... …Human EGR1 was amplified and cloned into the pCMV6-AC-IRES-GFP-Puro vector to tag EGR1 with Myc and FLAG (Origene Technologies, Rockville, MD, USA). 293T
DBA/2J Haplotype on Distal Chromosome 2 Reduces Mertk Expression, Restricts Efferocytosis, and Increases Susceptibility to Atherosclerosis
Kayashima, Makhanova, Maeda
Arterioscler. Thromb. Vasc. Biol. (2017)
AI Summary: OriGene’s pCMV6-AC-IRES-GFP-Puro vector was used to clone PCR fragments for Mertk cDNA overexpression experiments, enabling the study of how Mertk levels affect phagocytosis and atherosclerosis susceptibility.
Snippet: The PCR 95 fragments were cloned into pCMV6 - AC - I RES - GFP - Puro vector (OriGene)
Showing 1-6 of 13 papers.
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