Dextran, Fluorescein, 500,000 MW, Anionic, Lysine Fixable
Dextran, Fluorescein, 500,000 MW, Anionic, Lysine Fixable
Invitrogen™

Dextran, Fluorescein, 500,000 MW, Anionic, Lysine Fixable

Labeled dextrans are hydrophilic polysaccharides most commonly used in microscopy studies to monitor cell division, track the movement of liveRead more
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Catalog NumberQuantity
D713610 mg
Catalog number D7136
Price (USD)
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Quantity:
10 mg
Labeled dextrans are hydrophilic polysaccharides most commonly used in microscopy studies to monitor cell division, track the movement of live cells, and to report the hydrodynamic properties of the cytoplasmic matrix. The labeled dextran is commonly introduced into the cells via microinjection.

Need a different emission spectrum or longer tracking? View our other mammalian cell tracking products.

Dextran Specifications:

Label (Ex/Em): Fluorescein (494/521)
Size: 500,000 MW
Charge: Anionic
Fixable: Fixable via Lysine

High Manufacturing Standards of Molecular Probes™ Dextrans
We offer more than 50 fluorescent and biotinylated dextran conjugates in several molecular weight ranges. Dextrans are hydrophilic polysaccharides characterized by their moderate-to-high molecular weight, good water solubility, and low toxicity. They also generally exhibit low immunogeniticy. Dextrans are biologically inert due to their uncommon poly-(α-D-1,6-glucose) linkages, which render them resistant to cleavage by most endogenous cellular glycosidases.

In most cases, Molecular Probes™ fluorescent dextrans are much brighter and have higher negative charge than dextrans available from other sources. Furthermore, we use rigorous methods for removing as much unconjugated dye as practical, and then assay our dextran conjugates by thin-layer chromatography to help ensure the absence of low molecular weight contaminants.

A Wide Selection of Substituents and Molecular Weights
Molecular Probes™ dextrans are conjugated to biotin or a wide variety of fluorophores, including seven of our Alexa Fluor™ dyes (Molecular Probes dextran conjugates–Table 14.4) and are available in these nominal molecular weights (MW): 3,000; 10,000; 40,000; 70,000; 500,000; and 2,000,000 daltons.

Dextran Net Charge and Fixability
We employ succinimidyl coupling of our dyes to the dextran molecule, which, in most cases, results in a neutral or anionic dextran. The reaction used to produce the Rhodamine Green™ and Alexa Fluor 488 dextrans results in the final product being neutral, anionic, or cationic. The Alexa Fluor, Cascade Blue, lucifer yellow, fluorescein, and Oregon Green dextrans are intrinsically anionic, whereas most of the dextrans labeled with the zwitterionic rhodamine B, tetramethylrhodamine, and Texas Red™ dyes are essentially neutral. To produce more highly anionic dextrans, we have developed a proprietary procedure for adding negatively charged groups to the dextran carriers; these products are designated “polyanionic” dextrans.

Some applications require that the dextran tracer be treated with formaldehyde or glutaraldehyde for subsequent analysis. For these applications, we offer “lysine-fixable” versions of most of our dextran conjugates of fluorophores or biotin. These dextrans have covalently bound lysine residues that permit dextran tracers to be conjugated to surrounding biomolecules by aldehyde-mediated fixation for subsequent detection by immunohistochemical and ultrastructural techniques. We have also shown that all of our 10,000 MW Alexa Fluor dextran conjugates can be fixed with aldehyde-based fixatives.

Key Applications Using Labeled Dextrans
There are a multitude of citations describing the use of labeled dextrans. Some of the most common uses include:

Neuronal tracing (anterograde and retrograde) in live cells
Cell lineage tracing in live cells
Neuroanatomical tracing
Examining intercellular communications (e.g., in gap junctions, during wound healing, and during embryonic development)
Investigating vascular permeability and blood–brain barrier integrity
Tracking endocytosis
Monitoring acidification (some dextran–dye conjugates are pH-sensitive)
Studying the hydrodynamic properties of the cytoplasmic matrix

For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Label or DyeClassic Dyes
Product TypeDextran
Quantity10 mg
Shipping ConditionRoom Temperature
Excitation/Emission494/518 nm
Product LineInvitrogen
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Citations & References (20)

Citations & References
Abstract
Direct priming of antiviral CD8+ T cells in the peripheral interfollicular region of lymph nodes.
Authors:Hickman HD, Takeda K, Skon CN, Murray FR, Hensley SE, Loomis J, Barber GN, Bennink JR, Yewdell JW,
Journal:Nat Immunol
PubMed ID:18193049
'It is uncertain how antiviral lymphocytes are activated in draining lymph nodes, the site where adaptive immune responses are initiated. Here, using intravital microscopy we show that after infection of mice with vaccinia virus (a large DNA virus) or vesicular stomatitis virus (a small RNA virus), virions drained to the ... More
Intravital two-photon microscopy for studying the uptake and trafficking of fluorescently conjugated molecules in live rodents.
Authors:Masedunskas A, Weigert R,
Journal:Traffic
PubMed ID:18647170
'In this study, we describe an experimental system based on intravital two-photon microscopy for studying endocytosis in live animals. The rodent submandibular glands were chosen as model organs because they can be exposed easily, imaged without compromising their function and, furthermore, they are amenable to pharmacological and genetic manipulations. We ... More
T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases.
Authors:Mempel TR, Henrickson SE, Von Andrian UH
Journal:Nature
PubMed ID:14712275
'Primary T-cell responses in lymph nodes (LNs) require contact-dependent information exchange between T cells and dendritic cells (DCs). Because lymphocytes continually enter and leave normal LNs, the resident lymphocyte pool is composed of non-synchronized cells with different dwell times that display heterogeneous behaviour in mouse LNs in vitro. Here we ... More
Intracellular fluid flow in rapidly moving cells.
Authors:Keren K, Yam PT, Kinkhabwala A, Mogilner A, Theriot JA,
Journal:Nat Cell Biol
PubMed ID:19767741
'Cytosolic fluid dynamics have been implicated in cell motility because of the hydrodynamic forces they induce and because of their influence on transport of components of the actin machinery to the leading edge. To investigate the existence and the direction of fluid flow in rapidly moving cells, we introduced inert ... More
Vital staining of the hearing organ: visualization of cellular structure with confocal microscopy.
Authors:Flock A, Scarfone E, Ulfendahl M
Journal:Neuroscience
PubMed ID:9466411
'Cells inside the intact organ of Corti were labelled with fluorescent probes reflecting various aspects of structure and function. The dyes were introduced into the perilymphatic space by perfusion of the scala tympani of the temporal bone from the guinea-pig maintained in isolation. The dyes were able to diffuse through ... More