CellLight™ Lysosomes-GFP, BacMam 2.0
CellLight™ Lysosomes-GFP, BacMam 2.0
Invitrogen™

CellLight™ Lysosomes-GFP, BacMam 2.0

CellLight Lysosomes-GFP, BacMam 2.0, provides an easy way to label lysosomes with green fluorescent protein (GFP) in live cells. SimplyRead more
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Catalog NumberQuantity
C105961 mL
Catalog number C10596
Price (CNY)
6,960.00
Each
Add to cart
Quantity:
1 mL
Price (CNY)
6,960.00
Each
Add to cart
CellLight Lysosomes-GFP, BacMam 2.0, provides an easy way to label lysosomes with green fluorescent protein (GFP) in live cells. Simply add the reagent to your cells, incubate overnight, and the cells are ready to image in the morning.

Want to label other cell structures? Learn more about CellLight fluorescent protein labeling tools

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to lamp1 (lysosomal associated membrane protein 1). You can observe lysosomes-GFP behavior in live cells independently of organelle pH and label with multiple tracking or tracing dyes to image dynamic cellular processes.

Cells expressing CellLight constructs can also be fixed with formaldehyde for multiplexed imaging using immunocytochemical techniques.

CellLight Technology is:
Fast and convenient: simply add CellLight reagent to your cells, incubate overnight, and image—or store frozen, assay-ready cells for later use
Highly efficient: up to 90% transduction of a wide range of mammalian cell lines, including primary cells, stem cells, and neurons
Flexible: co-transduce more than one BacMam reagent for multiplex experiments or co-localization studies; tightly control expression levels by simply varying the dose
Less toxic: CellLight reagents are non-replicating in mammalian cells and are suitable for biosafety level (BSL) 1 handling

BacMam Technology
CellLight Lysosomes-GFP, BacMam 2.0, is a fusion construct of Lamp1 (lysosomal associated membrane protein 1) and emGFP, providing accurate and specific targeting to cellular lysosomes-GFP. This fusion construct is packaged in the insect virus baculovirus, which does not replicate in human cells and is designated as safe to use with biosafety level (BSL) 1 in most laboratories. BacMam technology ensures that most mammalian cell types are transduced/transfected with high efficiency and minimal toxicity. This transient transfection can be detected after overnight incubation for up to five days—enough time to carry out most dynamic cellular analyses. Like any transfection/transduction technique, the BacMam method does not transfect/transduce all of the cells with equal efficiency, making it poorly suited to cellular population studies or automated imaging/counting. CellLight reagents are ideal for experiments where cellular or subcellular co-locatization is required, or for cellular function studies that need special resolution.

Visualize staining your cell without wasting your reagents, antibodies, or time with our new Stain-iT Cell Staining Simulator.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorGreen
Detection MethodFluorescence
Dye TypeGFP (EmGFP)
EmissionVisible
Excitation Wavelength Range488⁄510
For Use With (Equipment)Confocal Microscope, Fluorescence Microscope
FormLiquid
Product LineCellLight
Quantity1 mL
Shipping ConditionWet Ice
TechniqueFluorescence Intensity
Label TypeFluorescent Dye
Product TypeLysosomal Probe
SubCellular LocalizationLysosomes
Unit SizeEach
Contents & Storage
Store at 2°C to 6°C, protected from light. Do Not Freeze.

Frequently asked questions (FAQs)

How can I increase the transduction efficiency with the BacMam 2.0 reagents such as the the CellLight and Premo products?

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.

Is there any way to preserve the CellLights labeling beyond 5 days?

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.

Are the CellLights products toxic to cells?

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.

For how long will the CellLights products label my cells?

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.

What cell types can the CellLights products be used with?

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 (26)

Citations & References
Abstract
Dynamic colocalization microscopy to characterize intracellular trafficking of nanomedicines.
Authors:Vercauteren D, Deschout H, Remaut K, Engbersen JF, Jones AT, Demeester J, De Smedt SC, Braeckmans K,
Journal:ACS Nano
PubMed ID:21923168
'To gain a better understanding of intracellular processing of nanomedicines, we employed quantitative live-cell fluorescence colocalization microscopy to study endosomal trafficking of polyplexes in retinal pigment epithelium cells. A new, dynamic colocalization algorithm was developed, based on particle tracking and trajectory correlation, allowing for spatiotemporal characterization of internalized polyplexes in ... More
The possible
Authors:Benjaminsen RV, Mattebjerg MA, Henriksen JR, Moghimi SM, Andresen TL,
Journal:Mol Ther
PubMed ID:23032976
Polycations such as polyethylenimine (PEI) are used in many novel nonviral vector designs and there are continuous efforts to increase our mechanistic understanding of their interactions with cells. Even so, the mechanism of polyplex escape from the endosomal/lysosomal pathway after internalization is still elusive. The  ... More
Inhibitors of intravesicular acidification protect against Shiga toxin in a pH-independent manner.
Authors:Dyve Lingelem AB, Bergan J, Sandvig K,
Journal:Traffic
PubMed ID:22132807
Shiga toxin inhibits protein synthesis after being transported from the cell surface to endosomes and retrogradely through the Golgi apparatus to the endoplasmic reticulum (ER) and into the cytosol. In this study, we have abolished proton gradients across internal membranes in different ways and investigated the effect on the various ... More
Effective endogenous gene silencing mediated by pH responsive peptides proceeds via multiple pathways.
Authors:Lam JK, Liang W, Lan Y, Chaudhuri P, Chow MY, Witt K, Kudsiova L, Mason AJ,
Journal:J Control Release
PubMed ID:22138072
Cationic amphipathic histidine rich peptides possess high plasmid DNA and siRNA delivery capabilities. To further understand the pH responsive siRNA delivery process and evaluate the capabilities of such peptides we have investigated their ability to mediate specific silencing of endogenous GAPDH gene activity in MCF-7 and A549 cells and compared ... More
Engineering of blended nanoparticle platform for delivery of mitochondria-acting therapeutics.
Authors:Marrache S, Dhar S,
Journal:Proc Natl Acad Sci U S A
PubMed ID:22991470
Mitochondrial dysfunctions cause numerous human disorders. A platform technology based on biodegradable polymers for carrying bioactive molecules to the mitochondrial matrix could be of enormous potential benefit in treating mitochondrial diseases. Here we report a rationally designed mitochondria-targeted polymeric nanoparticle (NP) system and its optimization for efficient delivery of various ... More