Dextran, Rhodamine B, 10,000 MW, Neutral
Dextran, Rhodamine B, 10,000 MW, Neutral
Invitrogen™

Dextran, Rhodamine B, 10,000 MW, Neutral

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
D182425 mg
Catalog number D1824
Price (CNY)
2,801.00
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Ends: 31-Dec-2025
3,796.00
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Quantity:
25 mg
Price (CNY)
2,801.00
飞享价
Ends: 31-Dec-2025
3,796.00
Save 995.00 (26%)
Each
Add to cart
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): Rhodamine B (570/590)
Size: 10,000 MW
Charge: Zwitterionic
Fixable: Nonfixable

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
Quantity25 mg
Shipping ConditionRoom Temperature
Excitation/Emission570/590 nm
Product LineInvitrogen
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Frequently asked questions (FAQs)

What is the excitation and emission wavelength for rhodamine?

Rhodamine is a generic term for a wide variety of cationic dyes whose fluorescence emission can range from green, orange to red. The table below lists the excitation and emission maxima (nm), as well as molar extinction coefficients (“EC”; cm-1 M-1), for various rhodamine dyes (data derived with dye dissolved in methanol).

Dye Excitation Emission EC
Rhodamine B 568 583 88,000
Rhodamine 123 507 529 101,000
Rhodamine 110 499 521 92,000
Rhodamine 6G 528 551 105,000
XRITC 572 596 92,000


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

Citations & References (23)

Citations & References
Abstract
Viscoelastic response of fibroblasts to tension transmitted through adherens junctions.
Authors:Ragsdale GK, Phelps J, Luby-Phelps K
Journal:Biophys J
PubMed ID:9370474
'Cytoplasmic deformation was monitored by observing the displacements of 200-nm green fluorescent beads microinjected into the cytoplasm of Swiss 3T3 fibroblasts. We noted a novel protrusion of nonruffling cell margins that was accompanied by axial flow of beads and cytoplasmic vesicles as far as 50 microm behind the protruding plasma ... More
Five-parameter fluorescence imaging: wound healing of living Swiss 3T3 cells.
Authors:DeBiasio R, Bright GR, Ernst LA, Waggoner AS, Taylor DL
Journal:J Cell Biol
PubMed ID:2444600
'Cellular functions involve the temporal and spatial interplay of ions, metabolites, macromolecules, and organelles. To define the mechanisms responsible for completing cellular functions, we used methods that can yield both temporal and spatial information on multiple physiological parameters and chemical components in the same cell. We demonstrated that the combined ... More
Confocal microscopy of intracellular calcium dynamics during fertilization.
Authors:Stricker SA
Journal:Biotechniques
PubMed ID:10997262
Calcium and endoplasmic reticulum dynamics during oocyte maturation and fertilization in the marine worm Cerebratulus lacteus.
Authors:Stricker SA, Silva R, Smythe T
Journal:Dev Biol
PubMed ID:9808782
'To monitor calcium and endoplasmic reticulum (ER) dynamics during oocyte maturation and fertilization, oocytes of the marine worm Cerebratulus lacteus were injected with the calcium-sensitive indicator calcium green dextran and/or the ER-specific probe "DiI." Based on time-lapse confocal imaging of such specimens, prophase-arrested immature oocytes failed to develop normally after ... More
Distinct roles of TIR and non-TIR regions in the subcellular localization and signaling properties of MyD88.
Authors:Nishiya T, Kajita E, Horinouchi T, Nishimoto A, Miwa S,
Journal:FEBS Lett
PubMed ID:17583698
MyD88 is a cytoplasmic adaptor protein that is critical for Toll-like receptor (TLR) signaling. The subcellular localization of MyD88 is characterized as large condensed forms in the cytoplasm. The mechanism and significance of this localization with respect to the signaling function, however, are currently unknown. Here, we demonstrate that MyD88 ... More