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Fluorescein-5-Isothiocyanate (FITC 'Isomer I')
Searching for superior alternatives to fluorescein? Our Alexa Fluor Dye Series offers everything you're looking for and more.Read more
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| Catalog Number | Quantity |
|---|---|
| F1906 | 10 x 10 mg |
| F1907 | 10 x 100 mg |
| F143 | 1 g |
Catalog number F1906
Price (USD)
202.00
Each
In stock
Quantity:
10 x 10 mg
Price (USD)
202.00
Each
Searching for superior alternatives to fluorescein? Our Alexa Fluor Dye Series offers everything you're looking for and more.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityAmine
Label or DyeFITC (Fluorescein)
Product TypeFluorescein-5-Isothiocyanate
Quantity10 x 10 mg
Reactive MoietyIsothiocyanate
Shipping ConditionRoom Temperature
Label TypeClassic Dyes
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.
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Figures
Proteobacterial symbionts. Fluorescein-5-isothiocyanate and Texas Red® sulfonyl chloride.
Chemical Structure
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Lot #Certificate TypeDateCatalog Number(s)
3193677Certificate of AnalysisJun 20, 2025F1906
3154628Certificate of AnalysisMay 18, 2025F1906
3136423Certificate of AnalysisMar 31, 2025F1906
3118566Certificate of AnalysisMar 31, 2025F1906
3135764Certificate of AnalysisMar 26, 2025F1907
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Citations & References (632)
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Citations & References
Abstract
Protonation dynamics of the extracellular and cytoplasmic surface of bacteriorhodopsin in the purple membrane.
Journal:Proceedings of the National Academy of Sciences of the United States of America
PubMed ID:8855251
The dynamics of proton binding to the extracellular and the cytoplasmic surfaces of the purple membrane were measured by laser-induced proton pulses. Purple membranes, selectively labeled by fluorescein at Lys-129 of bacteriorhodopsin, were pulsed by protons released in the aqueous bulk from excited pyranine (8-hydroxy-1,3,6-pyrenetrisulfonate) and the reaction of protons
The engineering of membrane-permeable peptides.
Journal:Analytical biochemistry
PubMed ID:15907875
Sensitive fluorescence-based thermodynamic and kinetic measurements of DNA hybridization in solution.
Journal:Biochemistry
PubMed ID:8457571
Kinetic and thermodynamic constants associated with DNA hybridization were determined in solution using fluorescence measurements and complementary fluorophore-labeled oligomers. One oligomer was labeled with a 5'-terminal fluorescein, and the other was labeled with a 3'-terminal rhodamine. The juxtaposition of the two labels in double-stranded complexes results in a strong quenching
Fluorescence resonance energy transfer analysis of the structure of the four-way DNA junction.
Journal:Biochemistry
PubMed ID:1591245
We have carried out fluorescence resonance energy transfer (FRET) measurements on four-way DNA junctions in order to analyze the global structure and its dependence on the concentration of several types of ions. A knowledge of the structure and its sensitivity to the solution environment is important for a full understanding
Macrophage phagocytosis: use of fluorescence microscopy to distinguish between extracellular and intracellular bacteria.
Journal:J Immunol Methods
PubMed ID:1919019
One of the challenges of phagocytosis research is to differentiate bacteria adherent to a host cell from bacteria which the cell has internalized. To address this question, various techniques such as fluorescence microscopy, electron microscopy, and flow cytometry have been used. We have adapted a flow cytometric method (Fattorossi et
632 total citations