pCMV6-A-GFP Mammalian Expression Vector

SKU
PS100026
pCMV6-A-GFP, mammalian vector with independent tGFP expression, 10ug
  $670.00
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Specifications
Specifications
Product Data
E. coli Selection Ampicillin (100 ug/mL)
Expression Promoter CMV
Features
  • This vector is essentially the same as the pCMV6-Entry vector, except for the alternative selection marker (GFP replacing Neomycin). GFP can be used to monitor transfection efficiency or as a cell sorting marker.
  • TurboGFP (excitation/ emission max = 482/ 502 nm) is mainly intended for applications where fast appearance of bright fluorescence is crucial. It is specially recommended for cell and organelle labeling and tracking the promoter activity. Structually it forms dimer. Learn more about TurboGFP
  • There is no drug selection marker in this vector for mammalian cells.
  • The vector itself does not contain additional tag. If the insert is shuttled from pCMV6-Entry via SgfI/AscI and RsrII/MluI, it will express non-tagged protein. If the insert is shuttled from the pCMV6-Entry vector using SgfI/AscI and Pme I, then it will express Myc-DDK tagged protein.
  • V2_F Primer can be used to sequence the target sequence after cloning.
  • XL39_R 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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ADH1B, the adipocyte-enriched alcohol dehydrogenase, plays an essential, cell-autonomous role in human adipogenesis
Gautheron, Elsayed, Pistorio et al
Proc Natl Acad Sci U S A (2024) 121 (24), e2319301121 DOI: 10.1073/pnas.2319301121
Cited by 17
AI Summary: In this study, OriGene products pCMV6-entry-GFP and pCMV-ADH1B WT-Flag were used as plasmid constructs to investigate the function of ADH1B in human adipocyte differentiation.
Snippet: ty Kit Thermo Fisher Scientific Cat# TR22421 TurboFect Thermo Fisher Scientific Cat# R0532 Recombinant DNA lentiCRISPR v2 Addgene Cat# 52961 pCMV6-entry-GFP Origene Cat# PS100026 pCMV-ADH1B WT-Flag Origene Cat# RC205391L3 pCMV-ADH1B c.937C>T-Flag Described in Methods N/A Software and Algorithms Multi-Experiment Viewer (MeV)
FigureFigureFigure
Individual expression and processing of hepatitis C virus E1/E2 epitopes-based DNA vaccine candidate in healthy humans' peripheral blood mononuclear cells
Nadeem, Maghraby, Abd-Elshafy et al
Clin Exp Vaccine Res (2023) 12 (1), 47-59 DOI: 10.7774/cevr.2023.12.1.47
Cited by 1
AI Summary: OriGene’s mammalian expression construct (PS100026) was used to clone and express the hepatitis C virus E1/E2 epitope DNA vaccine candidate in human peripheral blood mononuclear cells for evaluation in this study.
Snippet: sequence was submitted to the BepiPred-2.0: Sequential B-Cell Epitope Predictor Immune Epitope Database tool. The E1/T2A/E2 sequence was synthesized and inserted in a mammalian expression construct (OriGene PS100026;OriGene, Rockville, MD, USA) under the control of a cytomegalovirus promotor (synthesized via Blue Heron Biotech LLC, Bothell, WA, USA) (envelope epitopes construct abbreviated as EC
FigureFigureFigure
A Longitudinal and Transancestral Analysis of DNA Methylation Patterns in Systemic Lupus Erythematosus
Coit
Thesis (2022)
Snippet: We wanted to explore the role of TREML4 overexpression in neutrophil-like PLB-985 cells receiving TLR7 stimulation. A made-to-order TREML4 open reading frame clone (RC211020;OriGene, Rockville, MD, USA) was inserted into a pCMV6-A-GFP backbone (PS100026;OriGene, Rockville, MD, USA) un
Long noncoding RNA MEG3 blocks telomerase activity in human liver cancer stem cells epigenetically
Jiang, wang, xie et al
Research Square (2020)
Snippet: Ltd. pCMV6-A-GFP, pGFP-V-RS and pMirTarget-3'UTR pMirTarget-3'UTR were purchased from Origene (Rockville, MD,USA). pCMV6-A-GFP-MEG3, pGFP-V-RS-C- MEG3, pGFP-V-RS-TERT and pMartarget-3'UTR-C-TERT promoter were cloned by ourselves
Macrophage de novo NAD+ synthesis specifies immune function in aging and inflammation
Minhas, Liu, Moon et al
Nat. Immunol. (2019) 20 (1), 50-63 DOI: 10.1038/s41590-018-0255-3
AI Summary: OriGene products, specifically the pCMV6-QPRT-Myc-DDK-tagged plasmid and the pCMV6-A-GFP-tagged cloning vector, were used for overexpression and control experiments to investigate the role of QPRT in macrophage NAD+ synthesis and immune function.
Snippet: Plasmid-containing human QPRT (pCMV6-QPRT-Myc-DDK-tagged clone;OriGene) or control GFP (2 μg) (pCMV6-A-GFP-tagged cloning vector;OriGene) were incubated with a mixture of nucleofection solution and P4 primary cell supplement (82 μl:18 μl nucleofection solution:supplement) and placed in nucleofection cuvettes
Long noncoding RNA HULC accelerates liver cancer by inhibiting PTEN via autophagy cooperation to miR15a
Xin, Wu, Meng et al
Mol. Cancer (2018) 17 (1), 94 DOI: 10.1186/s12943-018-0843-8
AI Summary: OriGene products, including the plasmids pGFP-V-RS, pCMV6-A-GFP, pCMV6-XL5-PTEN, pGFP-V-RS-PTEN, pGFP-V-RS-Sirt1, and pMiR-Target, were used in this study to manipulate gene expression and investigate the molecular mechanisms by which lncRNA HULC accelerates liver cancer progression.
Snippet: with 10% heat-inactivated fetal bovine serum (Gibco) in a humidified atmosphere of 5% CO 2 incubator at 37 °C. Plasmid pGFP-V-RS, pCMV6-A-GFP, pCMV6-XL5-PTEN, pGFP-V-RS-PTEN, pGFP-V-RS-Sirt1, pMiR-Target were purchased from Origene (Rockville Cached
FigureFigureFigure
Showing 1-6 of 17 papers.
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