CellMask™ Plasma Membrane Stains
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CellMask™ Plasma Membrane Stains
Invitrogen™

CellMask™ Plasma Membrane Stains

Invitrogen CellMask™ plasma membrane stains enable fast and uniform labeling of the plasma membrane in almost all cell types. These stains work rapidly and can be detected using standard microscope filter sets with any imaging instrument.
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Catalog NumberColor
C37608Green
C10046Deep Red
C10045Orange
Catalog number C37608
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Color:
Green
Price (CNY)
2,583.00
Online Exclusive
Ends: 31-Dec-2025
3,502.00
Save 919.00 (26%)
Each
Add to cart
Invitrogen CellMask™ plasma membrane stains enable fast and uniform labeling of the plasma membrane in almost all cell types. These stains works rapidly and can be detected using standard microscope filter sets with any imaging instrument. Depending upon the cell type and experimental conditions, the plasma membrane staining will last for 60–90 minutes without detectable internalization, providing enough time for most live cell dynamic studies. The stain survives fixation, but not permeabilization.
Invitrogen CellMask™ plasma membrane stains enable fast and uniform labeling of the plasma membrane in almost all cell types. These stains works rapidly and can be detected using standard microscope filter sets with any imaging instrument. Depending upon the cell type and experimental conditions, the plasma membrane staining will last for 60–90 minutes without detectable internalization, providing enough time for most live cell dynamic studies. The stain survives fixation, but not permeabilization.

Features of CellMask™ plasma membrane stains include:
• Sensitivity—specific and rapid plasma membrane staining
• Excellent retention—staining lasts for 60–90 minutes
• Available in most common microscope channels, green, orange, deep red, and near infrared

Drawbacks of other methods
The plasma membrane is a convenient marker of cell boundaries and as such, a number of probes have been used for staining of the membrane. Typically, dyes of a lipophilic nature are used; however, they internalize rapidly, offering a very narrow window for imaging. Fluorescently labeled lectins, such as wheat germ agglutinin, have also been employed as plasma membrane stains. Conjugated lectins depend on cell surface sugars for staining and as a result, stain inconsistently with variation across cell types. Robust plasma membrane staining is important for a range of applications including translocation assays, plasma membrane dynamics, and as a general tool for cell identification in traditional and automated imaging and analysis.

How CellMask™ plasma membrane stains work
CellMask™ plasma membrane stains are designed to deliver uniform staining of the plasma membrane across a wide variety of mammalian cell types and are slow to internalize, particularly compared to traditional approaches such as DiI, DiO, and labeled wheat germ agglutinin.

CellMask™ plasma membrane stains are amphipathic molecules containing a lipophilic moiety for excellent membrane loading and a negatively charged hydrophilic dye for anchoring of the probe in the plasma membrane. While CellMask™ plasma membrane stains provide ample opportunity for live cell imaging, the staining pattern is also maintained after fixation with formaldehyde, enabling additional multiparametric imaging options. However, staining with CellMask™ plasma membrane stains does not survive detergent extraction and, therefore, cannot be used in conjunction with probes that require permeabilization.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorGreen
DescriptionCellMask™ Green Plasma Membrane Stain
For Use With (Equipment)Confocal Microscope, Fluorescence Microscope
Product LineCellmask
Quantity100 μL
Volume (Metric)100 μL
Label TypeFluorescent Dye
Product TypePlasma Membrane Stain
SubCellular LocalizationPlasma Membrane
Unit SizeEach
Contents & Storage
Store in freezer (–5° to –30°C) and protect from light.

Frequently asked questions (FAQs)

Can I use CellMask Plasma membrane stains or Alexa Fluor dye labeled wheat germ agglutinin to label the plasma membrane of my paraffin sections?

No. For paraffin sections, there are few options due to the delipidation of the membranes by solvents used in the deparaffinization steps. The only good option is to use an antibody against a plasma membrane protein.

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

How long does the staining last with CellMask Plasma Membrane Stains?

Depending upon the cell type and experimental conditions, the plasma membrane staining will last for 60-90 min without detectable internalization, providing enough time for most live cell dynamic studies. The stain survives fixation, but not permeabilization.

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

What dyes are used to make the CellMask stains?

The proprietary fluorescent dyes in the CellMask stains are general cytoplasmic stains. They are not found to bind to any specific cellular component.

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

I want to label the plasma membrane of my cells, but there are several dyes to choose from. Which one should I use?

For live-cell imaging, the CellVue and CellMask Plasma Membrane Stains are the most uniform and the slowest to be endocytosed. However, they are not the best choice if you wish to fix and permeabilize your cells, such as for antibody labeling. Wheat germ agglutinin (WGA) conjugates are also able to label live cells, or can label already formaldehyde-fixed cells. They can survive subsequent permeabilization with detergents, such as Triton X-100. If cells are already permeabilized, WGA will label internal structures as well. Thus, only an antibody against a plasma membrane protein can be used if cells are already permeabilized. Lipophilic cyanine dyes, such as DiI, will label all cell membranes in live cells, not just plasma membranes, if left on live cells for extended periods. Following page will help you choose (http://www.thermofisher.com/us/en/home/life-science/cell-analysis/cell-structure/plasma-membrane.html).

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

Citations & References (6)

Citations & References
Abstract
BAR scaffolds drive membrane fission by crowding disordered domains.
Authors:Snead WT, Zeno WF, Kago G, Perkins RW, Richter JB, Zhao C, Lafer EM, Stachowiak JC
Journal:J Cell Biol
PubMed ID:30504247
'Cellular membranes are continuously remodeled. The crescent-shaped bin-amphiphysin-rvs (BAR) domains remodel membranes in multiple cellular pathways. Based on studies of isolated BAR domains in vitro, the current paradigm is that BAR domain-containing proteins polymerize into cylindrical scaffolds that stabilize lipid tubules. But in nature, proteins that contain BAR domains often ... More
Altering integrin engagement regulates membrane localization of K
Authors:Sengupta S, Rothenberg KE, Li H, Hoffman BD, Bursac N
Journal:J Cell Sci
PubMed ID:31391240
How ion channels localize and distribute on the cell membrane remains incompletely understood. We show that interventions that vary cell adhesion proteins and cell size also affect the membrane current density of inward-rectifier K ... More
Anchoring cortical granules in the cortex ensures trafficking to the plasma membrane for post-fertilization exocytosis.
Authors:Vogt EJ, Tokuhiro K, Guo M, Dale R, Yang G, Shin SW, Movilla MJ, Shroff H, Dean J
Journal:Nat Commun
PubMed ID:31118423
Following fertilization, cortical granules exocytose ovastacin, a metalloendopeptidase that cleaves ZP2 in the zona pellucida surrounding mouse eggs to prevent additional sperm binding. Using high- and super-resolution imaging with ovastacin ... More
Membrane Mechanical Properties Regulate the Effect of Strain on Spontaneous Electrophysiology in Human iPSC-Derived Neurons.
Authors:Bianchi F, Pereno V, George JH, Thompson MS, Ye H
Journal:Neuroscience
PubMed ID:30817953
Peripheral nerves contain neuron fibers vital for movement and sensation and are subject to continuous elongation and compression during everyday movement. At supraphysiological strains conduction blocks occur, resulting in permanent or temporary loss of function. The mechanisms underpinning these alterations in electrophysiological activity remain unclear; however, there is evidence that ... More
Novel Analytical Platform For Robust Identification of Cell Migration Inhibitors.
Authors:Somchai P, Phongkitkarun K, Kueanjinda P, Jamnongsong S, Vaeteewoottacharn K, Luvira V, Okada S, Jirawatnotai S, Sampattavanich S
Journal:Sci Rep
PubMed ID:31969633
Wound healing assay is a simple and cost-effective in vitro assay for assessing therapeutic impacts on cell migration. Its key limitation is the possible confoundment by other cellular phenotypes, causing misinterpretation of the experimental outcome. In this study, we attempted to address this problem by developing a simple analytical approach ... More