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Empty Vector Ctrl ORF cDNA Lentiviral Plasmid
$795.00 – $895.00Price range: $795.00 through $895.00
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[Enter Gene Common Name] ([Enter Gene Alt Abbreviation]) ORF cDNA expression plasmid[[, available in both wild-type and [Enter Mutant] mutant forms], include only if applicable]. This plasmid encodes the full-length [Enter Gene Common Name] ORF cDNA under control of a CMV promoter. Supplied as transfection-ready DNA, the vector is suitable for direct transfection into mammalian cells or for packaging into lentiviral particles using compatible systems.
These constructs are designed to support high gene expression and stable genomic integration when used in lentiviral workflows, enabling efficient gene delivery to a wide range of cell types—including primary and previously frozen cells. Each construct may include a C-terminal tag, a fluorescent reporter (e.g., EGFP or mCherry), and/or a selection marker. Tag, reporter, and selection marker elements are fused or linked by self-cleaving peptide sequences depending on the product configuration. All plasmids are fully sequence-verified and validated in transient transfection assays.
Available Options:
Specifications
Lentiviral ORF cDNA Expression Plasmids
Overview
These plasmids enable high-level expression of the indicated ORF cDNA in mammalian cells following transfection. Each vector is optimized for efficient gene expression and can be used to generate high-titer lentiviral particles when co-transfected with compatible packaging plasmids. These constructs support long-term applications such as stable cell line development and include options for fluorescent (e.g., EGFP, mCherry) or luminescent (e.g., firefly luciferase) reporters.
Transcription of the C-terminally tagged ORF cDNA is driven by either the CMV or EF1α promoter. Reporter or drug selection markers (puromycin or blasticidin) are expressed separately using self-cleaving peptide sequences. In certain constructs, these markers are driven by the PGK promoter. The particles are suitable for transduction of various hard-to-transfect cell types, including primary and thawed cells. Cloning accuracy has been verified by sequencing, and expression has been confirmed via transient transfection.
Construct Design & Nomenclature
- Standard format: Promoter–ORFcDNA–Tag–T2A–Reporter–P2A–SelectionMarker
- Self-cleaving peptide shorthand: T2A and P2A sequences are denoted using slashes (“/”) in product names. Example:
Gene-V5/Reporter/SelectionMarkerrepresents Gene-V5–T2A–Reporter–P2A–SelectionMarker. - Fusion constructs: A hyphen (“–”) denotes a direct fusion. Example:
Gene-Reporter= Gene is fused directly to the reporter. - All tags (e.g., Flag, V5, HA) are fused to the C-terminus of the ORF cDNA by default, unless stated otherwise.
- Abbreviations: GFP = EGFP; RFP = mCherry.
- For any product inquiries, contact us at info@lipexogen.com.
Key Advantages
- Optimized Vectors – LipExoGen ORF cDNA expression plasmids are built on a third-generation lentiviral-compatible backbone. These vectors have been extensively optimized for stable, high-level gene expression in mammalian cells with minimal toxicity. Ideal for use in transfection workflows or lentiviral packaging. Constructs feature a C-terminally tagged ORF driven by CMV or EF1α and may include one or two markers (GFP, RFP, firefly luciferase, puromycin, or blasticidin), separated by self-cleaving peptides. Some layouts feature independent marker expression from a PGK promoter.
- Versatile Readouts – C-terminal tags (e.g., V5, Myc, HA) allow for detection by tag-specific antibodies in fixed cells or lysates. In live cells, drug selection and FACS sorting using GFP or RFP enable rapid identification of successfully transfected or transduced cells. Reporter fluorescence can be monitored via microscopy or flow cytometry. Luciferase constructs support sensitive quantification or in vivo imaging (e.g., IVIS) when packaged as virus.
- Flexible for Stable Line Generation – These plasmids are compatible with lentiviral packaging systems, enabling stable integration when needed. For transient studies, direct transfection yields robust expression. Stable cell lines can typically be generated within 10 days using antibiotic selection or FACS.
- Ready-to-Use Format – Supplied in PCR-grade water as high-purity, transfection-ready DNA. Each lot is thoroughly quality-tested for sequence integrity and yield, making it suitable for immediate use in transfection or lentiviral packaging. Ideal for fast-moving research workflows.
- Best Value & Customization – Every product is sequence-verified and expression-validated. Competitive pricing with free customization options, including promoter swaps, tag or reporter changes, and alternate marker configurations. Most custom requests are fulfilled within 10 days—just contact us.
Product Details
| Transfection-ready plasmid DNA | |
| PCR-grade water | |
| PEG precipitation and sucrose gradient centrifugation | |
| One vial | |
| 50 μl/vial | |
| 1–5×10⁶ TU/vial, depending on the variant | |
| 3×10⁸ VP/ml | |
| -20°C |
Recommended Control
Empty Vector Ctrl ORF cDNA Lentiviral Plasmid
Custom Orders
If you need to modify a product—such as changing the reporter or another vector component—please request a custom order. We offer fast, efficient custom cloning and high-quality lentiviral particle production, often at the same or lower price as catalog items.
If your gene of interest or transcript variant isn’t listed in our catalog, just let us know using one of the links below.
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