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引用和文献 (629)
Invitrogen™
荧光素-5-异硫氰酸盐（FITC异构体 I）
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| 货号 | 数量 |
|---|---|
| F143 | 1 g |
| F1907 | 10 x 100 mg |
| F1906 | 10 x 10 mg |
货号 F143
价格（CNY)
4,698.00
Each
数量:
1 g
价格（CNY)
4,698.00
Each
在寻找卓越的荧光素替代品？Alexa Fluor 染料系列为您提供所需的一切甚至更多。
仅供科研使用。不可用于诊断程序。
规格
化学反应性胺
标签或染料FITC(荧光素)
产品类型荧光素-5-异硫氰酸酯
数量1 g
反应一部分异硫氰酸盐
运输条件室温
标签类型经典染料
Unit SizeEach
内容与储存
储存在冰箱(-5 至 -30°C)中并避光。
引用和文献 (629)
引用和文献
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