Transferrin From Human Serum, Alexa Fluor™ Conjugate
Invitrogen™

Transferrin From Human Serum, Alexa Fluor™ Conjugate

Transferrin is a monomeric serum glycoprotein that binds to a specific receptor on the surface of vertebrate cells and delivers up to two Fe3+ atoms via receptor-mediated endocytosis—our labeled LDL complexes are useful tools for studying this phenomenon.
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Catalog NumberDye TypeQuantity
T13343Alexa Fluor Dyes5 mg
T13342Alexa Fluor Dyes5 mg
T2871Classic Dyes5 mg
T23364Alexa Fluor Dyes5 mg
T35352Alexa Fluor Dyes5 mg
T23365Alexa Fluor Dyes5 mg
T23362Alexa Fluor Dyes5 mg
T23366Alexa Fluor Dyes5 mg
Catalog number T13343
Price (EUR)
762,00
5 mg
Dye Type:
Alexa Fluor Dyes
Quantity:
5 mg
Price (EUR)
762,00
5 mg

Fluorescent transferrin for receptor-mediated endocytosis and recycling

Fluorescent transferrin conjugates are widely used to study transferrin receptor-mediated endocytosis, endosomal trafficking, and recycling using live-cell imaging or fixed-cell endpoint analysis. Transferrin binds transferrin receptor 1 (TfR1) at the cell surface and is internalized through clathrin-mediated endocytosis. Following endosomal acidification and iron release, apo-transferrin remains bound to TfR1 and the complex recycles to the plasma membrane, where apo-transferrin dissociates.

Why use fluorescent transferrin for endocytosis studies?

  • Track receptor-mediated endocytosis: Follow transferrin binding, TfR-mediated internalization, and intracellular trafficking.
  • Monitor endocytic recycling: Use fluorescent transferrin as a well-established marker of the endosomal recycling pathway.
  • Study trafficking kinetics: Follow uptake and recycling using live-cell imaging, pulse-chase experiments, or fixed-cell endpoint analysis.
  • Assess endosomal trafficking: Investigate trafficking events associated with endosomal acidification, cargo sorting, and membrane transport.
  • Compare trafficking pathways: Combine fluorescent transferrin with fluorescent LDL or other cargo markers to compare recycling and lysosomally directed pathways.
  • Enable multiplex fluorescence imaging: Choose from fluorescein and Alexa Fluor™ 488, 546, 555, 568, 594, 633, and 647 conjugates for multicolor imaging workflows.

Fluorescent transferrin enables a direct fluorescence readout of a well-characterized endocytic pathway, making it a versatile probe for studying receptor internalization, endosomal trafficking, and recycling.

Choose a fluorescent transferrin conjugate for your imaging workflow

Select from fluorescein and Alexa Fluor™ 488, 546, 555, 568, 594, 633, and 647 transferrin conjugates, with fluorescence spanning green to far-red wavelengths.

Multiple fluorophore options

  • Match your imaging system: Select a conjugate compatible with available excitation sources, emission filters, and detectors.
  • Support multicolor imaging: Choose spectrally distinct labels for use with antibodies, organelle markers, and other fluorescent probes.
  • Optimize experimental design: Select the excitation and emission profile that best fits your available fluorescence channels.
  • Use one biological probe across workflows: Study transferrin receptor trafficking with fluorophore options suitable for a range of fluorescence microscopy applications.

Applications of fluorescent transferrin

Fluorescent transferrin is a well-established probe for studying transferrin receptor-mediated endocytosis and intracellular trafficking.

Use fluorescent transferrin to:

  • Visualize receptor-mediated internalization and recycling using live-cell imaging or fixed-cell endpoint analysis
  • Track endosomal trafficking using fluorescence and confocal microscopy
  • Study trafficking events associated with endosomal acidification and changes in endosomal function
  • Investigate transferrin receptor dynamics, including appropriately designed FRET-based studies
  • Measure transferrin receptor binding in mammalian and parasite model systems
  • Compare recycling and lysosomal trafficking using complementary fluorescent cargo markers
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence
Dye TypeAlexa Fluor Dyes
Excitation/Emission590/617
FormSolid
Protein FamilyTransferrin
Quantity5 mg
Shipping ConditionRoom Temperature
Product LineAlexa Fluor
Product TypeTransferrin
pH7.2
Unit Size5 mg
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Citations & References (42)

Citations & References
Abstract
Inhibition of caveolar uptake, SV40 infection, and beta1-integrin signaling by a nonnatural glycosphingolipid stereoisomer.
Authors:Singh RD, Holicky EL, Cheng ZJ, Kim SY, Wheatley CL, Marks DL, Bittman R, Pagano RE
Journal:J Cell Biol
PubMed ID:17371832
'Caveolar endocytosis is an important mechanism for the uptake of certain pathogens and toxins and also plays a role in the internalization of some plasma membrane (PM) lipids and proteins. However, the regulation of caveolar endocytosis is not well understood. We previously demonstrated that caveolar endocytosis and beta1-integrin signaling are ... More
The long and the short cycle. Alternative intracellular routes for trafficking of G-protein-coupled receptors.
Authors:Innamorati G, Le Gouill C, Balamotis M, Birnbaumer M
Journal:J Biol Chem
PubMed ID:11150299
'The C terminus of the human V2 vasopressin receptor contains multiple phosphorylation sites including a cluster of amino acids that when phosphorylated prevents the return of the internalized receptor to the cell surface. To identify the step where the recycling process was interrupted, the trafficking of the V2 receptor was ... More
Transfer of M2 muscarinic acetylcholine receptors to clathrin-derived early endosomes following clathrin-independent endocytosis.
Authors:Delaney KA, Murph MM, Brown LM, Radhakrishna H
Journal:J Biol Chem
PubMed ID:12093817
'Upon agonist stimulation, many G protein-coupled receptors such as beta(2)-adrenergic receptors are internalized via beta-arrestin- and clathrin-dependent mechanisms, whereas others, like M(2) muscarinic acetylcholine receptors (mAChRs), are internalized by clathrin- and arrestin-independent mechanisms. To gain further insight into the mechanisms that regulate M(2) mAChR endocytosis, we investigated the post-endocytic trafficking ... More
Identification and characterization of small molecules that inhibit intracellular toxin transport.
Authors:Saenz JB, Doggett TA, Haslam DB
Journal:Infect Immun
PubMed ID:17576758
'Shiga toxin (Stx), cholera toxin (Ctx), and the plant toxin ricin are among several toxins that reach their intracellular destinations via a complex route. Following endocytosis, these toxins travel in a retrograde direction through the endosomal system to the trans-Golgi network, Golgi apparatus, and endoplasmic reticulum (ER). There the toxins ... More
A burst of auxilin recruitment determines the onset of clathrin-coated vesicle uncoating.
Authors:Massol RH, Boll W, Griffin AM, Kirchhausen T
Journal:Proc Natl Acad Sci U S A
PubMed ID:16798879
'Clathrin-coated pits assemble on a membrane and pinch off as coated vesicles. The released vesicles then rapidly lose their clathrin coats in a process mediated by the ATPase Hsc70, recruited by auxilin, a J-domain-containing cofactor. How is the uncoating process regulated? We find that during coat assembly small and variable ... More