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.
製品番号(カタログ番号)
C10046濃赤
C37608Green
C10045オレンジ
C56129Near-infrared
製品番号(カタログ番号) C10046
価格(JPY)
42,100
Each
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色:
濃赤
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.
仕様
濃赤
濃度5 mg⁄ml
概要CellMask™ Deep Red Plasma Membrane Stain
検出法蛍光
使用対象 (装置)ハイコンテント装置
製品ラインCellMask
数量100 μL
出荷条件室温
容量(メートル法)100 μL
標識タイプFluorescent Dye
製品タイプ細胞膜染色剤
SubCellular Localization細胞膜
Unit SizeEach
組成および保存条件
フリーザー(-5°C∼-30°C)に保存し、遮光してください。

よくあるご質問(FAQ)

I'm labeling live cells with Vybrant DiI or DiD lipophilic cyanine dyes. DiI gives a nice even membrane labeling, but DiD is more "spotty". What can be done?

This is expected. DiD (which is far-red fluorescent) is never as uniform as DiI (which is orange fluorescent). If uniformity is desired, try increasing the label time and concentration, but it still isn't likely to be as uniform as DiI. CellMask Deep Red Plasma Membrane stain is much more uniform and is about the same wavelength as DiD. However, if you intend to do cell tracking over days, CellMask stain has not been tried for that application.

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

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.

引用および参考文献 (24)

引用および参考文献
Abstract
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
Specific effects of surface amines on polystyrene nanoparticles in their interactions with mesenchymal stem cells.
Authors:Jiang X, Dausend J, Hafner M, Musyanovych A, Röcker C, Landfester K, Mailänder V, Nienhaus GU,
Journal:Biomacromolecules
PubMed ID:20166675
'We have investigated the uptake of cationic polystyrene nanoparticles by mesenchymal stem cells (MSCs) using confocal fluorescence microscopy and flow cytometry. Two types of nanoparticles of about 100 nm diameter with similar zeta potentials were employed in this study, plain polystyrene (PS) nanoparticles and amino-functionalized polystyrene (NPS) nanoparticles, each carrying ... More
Accumulation of amyloid-like Aß1-42 in AEL (autophagy-endosomal-lysosomal) vesicles: potential implications for plaque biogenesis.
Authors:Ling D, Magallanes M, Salvaterra PM,
Journal:
PubMed ID:24521233
'Abnormal accumulation of Aß (amyloid ß) within AEL (autophagy-endosomal-lysosomal) vesicles is a prominent neuropathological feature of AD (Alzheimer''s disease), but the mechanism of accumulation within vesicles is not clear. We express secretory forms of human Aß1-40 or Aß1-42 in Drosophila neurons and observe preferential localization of Aß1-42 within AEL vesicles. ... More
Insights into the residence in lipid rafts of adenylyl cyclase AC8 and its regulation by capacitative calcium entry.
Authors:Pagano M, Clynes MA, Masada N, Ciruela A, Ayling LJ, Wachten S, Cooper DM,
Journal:Am J Physiol Cell Physiol
PubMed ID:19158400
'Adenylyl cyclases (ACs) are a family of critically important signaling molecules that are regulated by multiple pathways. Adenylyl cyclase 8 (AC8) is a Ca(2+) stimulated isoform that displays a selective regulation by capacitative Ca(2+) entry (CCE), the process whereby the entry of Ca(2+) into cells is triggered by the emptying ... More
Enterotoxigenic Escherichia coli secretes a highly conserved mucin-degrading metalloprotease to effectively engage intestinal epithelial cells.
Authors:Luo Q, Kumar P, Vickers TJ, Sheikh A, Lewis WG, Rasko DA, Sistrunk J, Fleckenstein JM,
Journal:
PubMed ID:24478067
'Enterotoxigenic Escherichia coli (ETEC) is a leading cause of death due to diarrheal illness among young children in developing countries, and there is currently no effective vaccine. Many elements of ETEC pathogenesis are still poorly defined. Here we demonstrate that YghJ, a secreted ETEC antigen identified in immunoproteomic studies using ... More