Cell Structure Reagents and Kits

DAPI is a fluorescent dye commonly used in molecular biology and cell biology research. DAPI is known for its ability to bind to DNA, specifically to the minor groove of double-stranded DNA. This dye emits blue fluorescence when excited by ultraviolet li

SYTOX Green nucleic acid stain is an excellent green-fluorescent nuclear and chromosome counterstain that is impermeant to live cells.Simple Viability Determination SYTOX Green allows quick determination of cell viability when using flow cytometers, fluo

The intracellular accumulation of neutral lipids, steatosis, is often triggered by drugs that affect the metabolism of fatty acids and/or neutral lipids. HCS LipidTOX Deep Red neutral lipid stain was developed to characterize the potentially toxic effect

Rosamine & carbocyanine-based staining dyes MitoTracker Orange CMTMRos, Red CMXRos, Orange CM-H2TMRos, Red CM-H2XRos, Red FM, Green FM, & Deep Red FM enable mitochondria visualization with fluorescent imaging. These mitochondria dyes are specially packag

The Vybrant CM-DiI cell-labeling solution is a dye delivery solution that can be added directly to normal culture media to uniformly label suspended or attached culture cells for use in cell-cell fusion, cellular adhesion and migration applications.Cell

CFDA, SE is a fixable-cell-permeant, fluorescein-based tracer for very long-term cell labeling. The dye is also available in our convenient, easy-to-use Vybrant CFDA-SE Cell Tracer Kit (V12883).

7-aminoactinomycin D (7-AAD) is a fluorescent intercalator that undergoes a spectral shift upon association with DNA. 7-AAD/DNA complexes can be excited by the 488 nm laser and has an emission maxima of 647 nm, making this nucleic acid stain useful for m

Excitation of the ACMA-DNA complex (excitation/emission maxima ∽419/483nm) is possible with most UV-light sources, making it compatible for use with both shorter- and longer-wavelength dyes. ACMA also apparently binds to membranes in the energized state

Acridine Orange emits green fluorescence when bound to dsDNA and red fluorescence when bound to ssDNA or RNA. This unique characteristic makes acridine orange useful for cell-cycle studies. Acridine orange has also been used as a lysosomal dye. This dye

Acridine Orange emits green fluorescence when bound to dsDNA and red fluorescence when bound to ssDNA or RNA. This unique characteristic makes acridine orange useful for cell-cycle studies. Acridine orange has also been used as a lysosomal dye. This dye

To use, simply add the BacMam enhancer to cell culture media with or without serum that have already been treated with the BacMam reagent, then incubate cells for 1.5–2 hours at 37°C and 5% CO2 and replace with fresh medium. Different cell types vary in

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 photostable and this non-targeted for

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to human actin. You can observe actin-GFP behavior in live cells using a fluorescent imaging system and standard FITC/GFP filter se

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to human actin. You can observe actin-RFP behavior in live cells using a fluorescent imaging system and standard TRITC/RFP filter s

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to Rab5a. You can observe early endosomes-GFP behavior in live cells independently of organelle pH and label with multiple tracking or tracing

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to Rab5a. You can observe early endosomes-RFP behavior in live cells independently of organelle pH and label with multiple tracking or tracing

This ready-to-use construct is transfected into cells using BacMam 2.0 technology and expresses GFP fused to the ER signal sequence of calreticulin and KDEL (ER retention signal) with minimal cellular disruption. You can observe ER-GFP behavior in live c

This ready-to-use construct is transfected into cells using BacMam 2.0 technology and expresses RFP fused to the ER signal sequence of calreticulin and KDEL (ER retention signal) with minimal cellular disruption. You can observe ER-RFP behavior in live c

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to human golgi resident enzyme (N-acetylgalactosaminyltransferase). You can observe golgi-GFP behavior in live cells using fluorescent imaging

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to human golgi resident enzyme (N-acetylgalactosaminyltransferase). You can observe golgi-RFP behavior in live cells using fluorescent imaging

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to histone 2B. You can observe histone 2B-GFP behavior in live cells using fluorescent imaging with almost no cytotoxicity.Cells expressing Ce

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to Rab7a. You can observe late endosomes-GFP behavior in live cells independently of organelle pH and label with multiple tracking or tracing

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to Rab7a. You can observe late endosomes-RFP behavior in live cells independently of organelle pH and label with multiple tracking or tracing

This ready-to-use construct is transduced/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 using a fluorescent imagin

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to Lamp1 (lysosomal associated membrane protein 1). You can observe lysosomes-RFP behavior in live cells using a fluorescent imagin

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to the Leader sequence of E1 alpha pyruvate dehydrogenase. You can observe mitochondria-GFP behavior in live cells using a fluoresc

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to the Leader sequence of E1 alpha pyruvate dehydrogenase. You can observe mitochondria-RFP behavior in live cells using a fluoresc

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to the SV40 nuclear localization sequence. You can observe nucleus-GFP behavior in live cells without the cellular toxicity associated with in

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to the SV40 nuclear localization sequence. You can observe nucleus-RFP behavior in live cells without the cellular toxicity associated with in

CellLight Null Control contains no mammalian promoter and no transgene. CellLight reagents combine the utility and selectivity of fluorescent proteins with the transduction efficiency of BacMam technology, enabling unambiguous staining of organelles, cel

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to the peroxisomal C terminal targeting sequence. You can observe peroxisome-GFP behavior in live cells and use multiple tracking or tracing d

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses CFP fused to the myristolyation/palmitoylation sequence from Lck tyrosine kinase. You can observe plasma membrane-CFP behavior in live cells without sta

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to the myristolyation/palmitoylation sequence from Lck tyrosine kinase. You can observe plasma membrane-GFP behavior in live cells without sta

This ready-to-use construct is transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to the myristolyation/palmitoylation sequence from Lck tyrosine kinase. You can observe plasma membrane-RFP behavior in live cells without sta

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to the c terminus of human talin. You can observe talin-GFP behavior in live cells to study the focal adhesion of integrins and the

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses GFP fused to human tubulin. You can observe tubulin-GFP behavior in live cells using a fluorescent imaging system and standard FITC/GFP filte

This ready-to-use construct is transduced/transfected into cells using BacMam 2.0 technology, where it expresses RFP fused to human tubulin. You can observe tubulin-RFP behavior in live cells using a fluorescent imaging system and standard TRITC/RFP filt

Stain and track intracellular filamentous actin (F-actin) with the CellMask Actin Tracking Stain Variety Pack in live or fixed cells in immunofluorescence (IF), immunocytochemistry (ICC), and immunohistochemistry (IHC) protocols, and in 3D cell culture.

Stain and track intracellular F-actin with CellMask Deep Red Actin Tracking Stain in live or fixed cells in immunofluorescence (IF), immunocytochemistry (ICC), and immunohistochemistry (IHC) protocols, and in 3D cell culture. The CellMask Deep Red Actin

Stain and track intracellular F-actin with CellMask Green Actin Tracking Stain in live or fixed cells in immunofluorescence (IF), immunocytochemistry (ICC), and immunohistochemistry (IHC) protocols, and in 3D cell culture. The CellMask Green Actin Tracki

Stain and track intracellular F-actin with CellMask Orange Actin Tracking Stain in live or fixed cells in immunofluorescence (IF), immunocytochemistry (ICC), and immunohistochemistry (IHC) protocols, and in 3D cell culture. The CellMask Orange Actin Trac

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

Readily permeates cell membranes and selectively stains mitochondria and endomembranous organelles such as endoplasmic reticulum and Golgi apparatus, but does not appear to localize in plasma membraneCell Adhesion, Cell Analysis, Cell Proliferation, Cell

CellTrace calcein blue AM is a proven short-term, blue-fluorescent tracer for cell labeling. The probe possesses acetoxymethyl (AM) esters that allow its passive diffusion across cell membranes. Upon cleavage of the AM esters by intracellular esterases,

CellTrace™ calcein violet AM is an optimal dye for distinguishing live cells through the presence of ubiquitous intracellular esterase activity. The enzymatic conversion of the virtually non-fluorescent cell-permeant calcein violet AM to the intensely fluorescent calcein violet (ex/em 400/452 nm) can be easily detected with the violet laser, allowing other laser lines to be used for conventional fluorochromes. View a selection guide for all Nonfixable Viability Dyes for Flow Cytometry.

After loading into cells, dye is well retained, allowing for multigenerational tracking of cellular movementsRed excitation/emission spectra (553/570nm maxima) are optimal for multiplexing with green fluorescent dyes and proteinsFluorescent signal retent

Cell movement and location studies require specialized probes that are nontoxic to living cells and well retained, allowing for multigenerational tracking. The CellTracker fluorescent probes are available in a range of fluorescent colors to match instrum

The lipophilic aminostyryl probe DiA inserts into membranes with its two alkyl tails and its fluorophore oriented parallel to the phospholipid acyl chain. When this dialkylaminostyryl probe binds to membranes, it exhibits a strong fluorescence enhancemen

The far-red fluorescent, lipophilic carbocyanine DiD is an oil at room temperature and weakly fluorescent in water but highly fluorescent and quite photostable when incorporated into membranes. It has an extremely high extinction coefficient and short ex

The far-red fluorescent, lipophilic carbocyanine DiD is a longer-wavelength DiI analog. It is supplied as a solid form to facilitate direct application of crystals to membranes and is weakly fluorescent in water but highly fluorescent and quite photostab