BacMam GFP Transduction Control (BacMam 2.0)
BacMam GFP Transduction Control (BacMam 2.0)
Invitrogen™

BacMam GFP Transduction Control (BacMam 2.0)

The BacMam 2.0 Transduction Control lets you experience the power and convenience of enhanced BacMam technology, with the convenient readoutRead more
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Catalog NumberQuantity
B103831 mL
Catalog number B10383
Price (EUR)
-
Quantity:
1 mL
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The BacMam 2.0 Transduction Control lets you experience the power and convenience of enhanced BacMam technology, with the convenient readout of emerald GFP (emGFP); our Aequorea victoria emGFP is extremely bright and photo stable and this non-targeted form is ideal for testing transduction. Check out how well BacMam 2.0 works with GFP in your model before advancing to the more specialized reagents.

BacMam 2.0 provides several advantages over other gene transfer methods:

• Efficient: highly efficient (>90%) transduction of a wide range of mammalian cell lines, including primary cells, stem cells and neuronal cells
Fast and convenient: Simply add the BacMam 2.0 together with cells to your cover slip or microtiter plate, incubate overnight and assay – or store frozen, assay-ready cells for later use
Safe: non-replicating in mammalian cells, lack of observable cytopathic effect and biosafety level (BSL) 1 handling
Enables Flexiblity: co-transduce more than one BacMam reagent for multiplex experiments or co-localization studies and tightly control expression levels by just varying the dose

The BacMam technology is based on an insect virus (baculovirus) to help efficiently deliver and express genes in mammalian cells. The baculovirus has been modified to include an expression cassette for transgene expression in mammalian cells. BacMam 2.0 incorporate elements that help greatly enhance transduction efficiency and expression levels: a pseudotyped capsid protein for more efficient cell entry and genetic elements (enhanced CMV promoter and Woodchuck Post-transcriptional Regulatory Element), that boost expression levels. Baculoviruses do not replicate in mammalian cells and thus have an excellent safety profile and lack cytopathic effects on cells.

Cell types previously not compatible with the technology (neuronal cells, T-cells), or only poorly transduced (some stem cells, CHO) are now transduced quantitatively in a simple, one step process.

We offer a range of BacMam-based reagents, including Cellular Lights™ cell labeling reagents, Premo™ Biosensors, ion channel drug targets, pathway analysis kits, and more. To learn more about these products, please visit www.invitrogen.com ⁄bacmam.

Today the other BacMam 2.0-based reagent is our enabling Premo™ Autophagy Sensor for autophagy research in live cells.

For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorGreen
Detection MethodFluorescence
Dye TypeGFP (EmGFP)
EmissionVisible
Excitation Wavelength Range485⁄520
For Use With (Equipment)Fluorescence Microscope, Fluorometer, HTS Reader, High Content Instrument, Flow Cytometer
FormLiquid
PromoterCMV
Quantity1 mL
Shipping ConditionWet Ice
TechniqueFluorescence Intensity
Label TypeFluorescent Dye
Product TypeBacMam GFP Transduction Control
SubCellular LocalizationCytoplasm, Nucleus
Unit SizeEach
Contents & Storage
The BacMam GFP ttransduction control contains 1 ml of virus at a concentration of approximately 1 × 10^8 viral particles⁄ml.
Approximate fluorescence excitation⁄emission maxima for emGFP: 485⁄520 in nm.
The BacMam transduction control should be stored at 4°C, protected from light. When stored as directed, it is stable for 6 months. DO NOT FREEZE.
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Fluorescence spectra

Fluorescence spectra

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Certificates

Lot #Certificate TypeDateCatalog Number(s)
3204177Certificate of AnalysisMay 18, 2025B10383
3123561Certificate of AnalysisMar 30, 2025B10383
2850310Certificate of AnalysisFeb 19, 2024B10383
2575966Certificate of AnalysisApr 03, 2023B10383
2415742Certificate of AnalysisFeb 25, 2022B10383
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Safety Data Sheets

Molecular Probes® Handbook

Frequently asked questions (FAQs)

Try varying particle-to-cell ratio (PPC), incubation volume, temperature and, cell density (if adherent cells are transduced). For adherent cells, we recommend a confluence of about 70%. Following the PPC, adjusting the volume is the next best parameter to change to optimize protein expression. If that doesn't work, you can also use the BacMam Enhancer Kit (Cat. No. B10107).

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Cells transduced with the CellLights reagents can be stored frozen for several months after transduction, without loss of expression.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

If the viral particles are used at the level we recommend, they are very well tolerated by cells.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

The BacMam 2.0 CellLights typically express for 5 days after transduction.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

The first generation BacMam reagents were shown to efficiently transduce over 90 cell types, including stable cell lines and primary cells. With BacMam 2.0, it is now possible to also efficiently transduce primary neurons and stem cells.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Citations & References (2)

Citations & References
Abstract
BacMam technology and its application to drug discovery.
Authors:Ames RS, Kost TA, Condreay JP,
Journal:Expert Opin Drug Discov
PubMed ID:23488908
The recombinant baculovirus/insect cell system was firmly established as a leading method for recombinant protein production when a new potential use for these viruses was revealed in 1995. It was reported that engineered recombinant baculoviruses could deliver functional expression cassettes to mammalian cell types; a system which has come to ... More
Baculovirus-mediated gene transfer into mammalian cells.
Authors:Boyce FM, Bucher NL,
Journal:Proc Natl Acad Sci U S A
PubMed ID:8637876
This paper describes the use of the baculovirus Autographa californica multiple nuclear polyhedrosis virus (AcMNPV) as a vector for gene delivery into mammalian cells. A modified AcMNPV virus was prepared that carried the Escherichia coli lacZ reporter gene under control of the Rous sarcoma virus promoter and mammalian RNA processing ... More
2 total citations

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