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FD20S

Sigma-Aldrich

Fluorescein isothiocyanate–dextran

average mol wt 20,000

Synonym(s):

FITC–Dextran

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1 KIT
CN¥11,569.45
5 X 1 KIT
CN¥46,289.42

CN¥11,569.45


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1 KIT
CN¥11,569.45
5 X 1 KIT
CN¥46,289.42

About This Item

CAS Number:
MDL number:
UNSPSC Code:
12352201
NACRES:
NA.25

CN¥11,569.45


Please contact Customer Service for Availability

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biological source

sugar beets root

Quality Level

conjugate

FITC conjugate

form

powder

mol wt

average mol wt 20,000

extent of labeling

0.003-0.020 mol FITC per mol glucose

color

yellow to dark yellow

solubility

water: 25 mg/mL

storage temp.

2-8°C

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1 of 4

This Item
Z677698Z677728Z677647
feature

CE compliant, powder-free: no, standard type EN 374 (cat. III), latex free, standard type EN 388 (cat. III), reusable

feature

CE compliant, latex free, powder-free: no, reusable, standard type EN 374 (cat. III), standard type EN 388 (cat. III)

feature

CE compliant, latex free, powder-free: no, reusable, standard type EN 374 (cat. III), standard type EN 388 (cat. III)

feature

CE compliant, latex free, powder-free: no, reusable, standard type EN 374 (cat. III), standard type EN 388 (cat. III)

material

black (fluorocarbon rubber), black gloves

material

black (fluorocarbon rubber), black gloves

material

black (fluorocarbon rubber), black gloves

material

black butyl rubber , black gloves

manufacturer/tradename

KCL 890

manufacturer/tradename

KCL 890

manufacturer/tradename

KCL 890

manufacturer/tradename

KCL 897

packaging

pack of 1 pair

packaging

pack of 1 pair

packaging

pack of 1 pair

packaging

pack of 1 pair

size

XL (11)

size

S (8)

size

L (10)

size

M

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

General description

Dextran is a polymer of anhydroglucose. It is composed of approximately 95% alpha-D-(166) linkages. The remaining (163) linkages account for the branching of dextran. Conflicting data on the branch lengths implies that the average branch length is less than three glucose units. However, other methods indicate branches of greater than 50 glucose units exist. Native dextran has been found to have a molecular weight (MW) in the range of 9 million to 500 million. Lower MW dextrans will exhibit slightly less branching and have a more narrow range of MW distribution. Dextrans with MW greater than 10,000 behave as if they are highly branched. As the MW increases, dextran molecules attain greater symmetry. Dextrans with MW of 2,000 to 10,000, exhibit the properties of an expandable coil. At MW below 2,000, dextran is more rod-like. The MW of dextran is measured by one or more of the following methods: low angle laser light scattering, size exclusion chromatography, copper-complexation and anthrone reagent colorometric reducing-end sugar determination and viscosity.

Application

Dextran labeled with fluorescein isothiocyanate for possible use in perfusion studies in animals.
FITC-dextran is used extensively in microcirculation and cell permeability research utilizing microfluorimetry. FITC-dextran has been used to study plant cell wall porosity and capillary permeability. Plasma proteins have been shown not to bind to FITC-dextran.
FITC-dextran is used in cardiovascular, microcirculation, perfusion, cell monolayer and cell membrane permeability research as fluorescent flux tracer compound that supports the measurement of processes such as blood flow, membrane damage, vascular drainage and renal elimination.[1] Small FITC-dextrans are also used to measure processes such as endocytosis and cell junction permeability. Fluorescein-dextran, 20 kDa, may be used to study cell processes such as endocytosis and osmoporation.[2] FITC-dextran-20 may be used to study endothelial or epithelial monolayer porosity, apical-basolateral movements within cell layers and cell junction permeability. FITC-dextran-20 may be used as a model compound to study drug release from structures such as hydrogens and collagen minirods.[3]

Preparation Note

Sigma typically tests the solubility of FITC dextrans in water at concentrations at or above 25 mg/ml. Solutions should be protected from light. In vivo, FITC-dextran is stable for more than 24 hours.

Other Notes

Similar to FD-20, but produced by Sigma.
To gain a comprehensive understanding of our extensive range of Dextrans for your research, we encourage you to visit our Carbohydrates Category page.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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    Journal of the American Society for Mass Spectrometry, 21(9), 1606-1611 (2010-05-21)
    Shotgun proteomics has been used extensively for characterization of a number of proteomes. High-resolution Fourier transform mass spectrometry (FTMS) has emerged as a powerful tool owing to its high mass accuracy and resolving power. One of its major limitations, however
    Mark V Ivanov et al.
    Journal of proteome research, 13(4), 1911-1920 (2014-02-28)
    Data-dependent tandem mass spectrometry (MS/MS) is one of the main techniques for protein identification in shotgun proteomics. In a typical LC-MS/MS workflow, peptide product ion mass spectra (MS/MS spectra) are compared with those derived theoretically from a protein sequence database.
    Henrik Molina et al.
    Analytical chemistry, 80(13), 4825-4835 (2008-06-11)
    Electron transfer dissociation (ETD) is a recently introduced mass spectrometric technique which has proven to be an excellent tool for the elucidation of labile post-translational modifications such as phosphorylation and O-GlcNAcylation of serine and threonine residues. However, unlike collision induced
    Leslie Muller et al.
    Proteomics, 16(23), 2953-2961 (2016-10-18)
    Sample preparation, typically by in-solution or in-gel approaches, has a strong influence on the accuracy and robustness of quantitative proteomics workflows. The major benefit of in-gel procedures is their compatibility with detergents (such as SDS) for protein solubilization. However, SDS-PAGE
    Markus Brosch et al.
    Molecular & cellular proteomics : MCP, 7(5), 962-970 (2008-01-25)
    It is a major challenge to develop effective sequence database search algorithms to translate molecular weight and fragment mass information obtained from tandem mass spectrometry into high quality peptide and protein assignments. We investigated the peptide identification performance of Mascot

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