CellMask™ Plasma Membrane Stains
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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카탈로그 번호색상
C37608Green
C10046Deep Red
C10045Orange
C56129Near-infrared
카탈로그 번호 C37608
제품 가격(KRW)
437,000
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Ends: 30-Sep-2025
485,000
할인액 48,000 (10%)
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색상:
Green
제품 가격(KRW)
437,000
Online offer
Ends: 30-Sep-2025
485,000
할인액 48,000 (10%)
Each
카트에 추가하기
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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.
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Certificates | 증명서

Lot 번호Certificate TypeDateCatalog Number(s)
3188279Certificate of Analysis2025년 6월 29일C10045
3212673Certificate of Analysis2025년 5월 16일C56129
3143062Certificate of Analysis2025년 4월 03일C10045
3143943Certificate of Analysis2025년 4월 03일C10046
AC410173Certificate of Analysis2025년 3월 20일C56129
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Safety Data Sheets | 물질 안전 보건 자료

자주 묻는 질문(FAQ)

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.

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.

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.

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.

인용 및 참조 문헌 (64)

인용 및 참조 문헌
Abstract
Amino acid residues critical for endoplasmic reticulum export and trafficking of platelet-activating factor receptor.
Authors:Hirota N, Yasuda D, Hashidate T, Yamamoto T, Yamaguchi S, Nagamune T, Nagase T, Shimizu T, Nakamura M,
Journal:J Biol Chem
PubMed ID:20007715
'Several residues are conserved in the transmembrane domains (TMs) of G-protein coupled receptors. Here we demonstrate that a conserved proline, Pro(247), in TM6 of platelet-activating factor receptor (PAFR) is required for endoplasmic reticulum (ER) export and trafficking after agonist-induced internalization. Alanine-substituted mutants of the conserved residues of PAFRs, including P247A, ... More
Binding of guanylyl cyclase activating protein 1 (GCAP1) to retinal guanylyl cyclase (RetGC1). The role of individual EF-hands.
Authors:Peshenko IV, Olshevskaya EV, Dizhoor AM,
Journal:J Biol Chem
PubMed ID:18541533
'Guanylyl cyclase activating protein 1 (GCAP1), after substitution of Ca(2+) by Mg(2+) in its EF-hands, stimulates photoreceptor guanylyl cyclase, RetGC1, in response to light. We inactivated metal binding in individual EF-hands of GCAP1 tagged with green fluorescent protein to assess their role in GCAP1 binding to RetGC1 in co-transfected HEK293 ... More
Thiazolides, a new class of anti-influenza molecules targeting viral hemagglutinin at the post-translational level.
Authors:Rossignol JF, La Frazia S, Chiappa L, Ciucci A, Santoro MG,
Journal:J Biol Chem
PubMed ID:19638339
'The emergence of highly contagious influenza A virus strains, such as the new H1N1 swine influenza, represents a serious threat to global human health. Efforts to control emerging influenza strains focus on surveillance and early diagnosis, as well as development of effective vaccines and novel antiviral drugs. Herein we document ... More
Common lymphatic endothelial and vascular endothelial receptor-1 mediates the transmigration of regulatory T cells across human hepatic sinusoidal endothelium.
Authors:Shetty S, Weston CJ, Oo YH, Westerlund N, Stamataki Z, Youster J, Hubscher SG, Salmi M, Jalkanen S, Lalor PF, Adams DH,
Journal:J Immunol
PubMed ID:21368224
'The common lymphatic endothelial and vascular endothelial receptor (CLEVER-1; also known as FEEL-1 and stabilin-1) is a recycling and intracellular trafficking receptor with multifunctional properties. In this study, we demonstrate increased endothelial expression of CLEVER-1/stabilin-1 at sites of leukocyte recruitment to the inflamed human liver including sinusoids, septal vessels, and ... More
The Giardia median body protein is a ventral disc protein that is critical for maintaining a domed disc conformation during attachment.
Authors:Woessner DJ, Dawson SC,
Journal:Eukaryot Cell
PubMed ID:22247266
'Giardia has unique microtubule structures, including the ventral disc, the primary organelle of attachment to the host, and the median body, a structure of undefined function. During attachment, the ventral disc has a domed conformation and enables Giardia to attach to the host intestinal epithelia within seconds. The mechanism of ... More
64 total citations

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