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引用和文献 (151)
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四甲基罗丹明-5-碘乙酰胺二氢碘化物 (5-TMRIA)（单异构体）
硫醇反应性四甲基罗丹明-5-碘乙酰胺二氢碘化物 (5-TMRIA) 可用于生成明亮橙红色荧光生物偶联物，最大激发/发射波长 ∼555/580。了解更多信息
| 货号 | 数量 |
|---|---|
| T6006 | 5 mg |
货号 T6006
价格（CNY)
7,335.00
5 mg
数量:
5 mg
价格（CNY)
7,335.00
5 mg
硫醇反应性四甲基罗丹明-5-碘乙酰胺二氢碘化物 (5-TMRIA) 可用于生成明亮橙红色荧光生物偶联物，最大激发/发射波长 ∼555/580。
仅供科研使用。不可用于诊断程序。
规格
化学反应性硫醇
发射580
激发555
标签或染料罗丹明异构体、TMR(四甲基罗丹明)
产品类型四甲基罗丹明-5-碘乙酰胺二氢碘化物
数量5 mg
反应一部分烷基卤化物、碘乙酰胺
运输条件室温
标签类型经典染料
Unit Size5 mg
内容与储存
储存在冰箱(-5 至 -30°C)中并避光。
引用和文献 (151)
引用和文献
Abstract
Rapid binding of synapsin I to F- and G-actin. A study using fluorescence resonance energy transfer.
Journal:FEBS Lett
PubMed ID:8365471
Synapsin I is a nerve terminal phosphoprotein which interacts with synaptic vesicles and actin in a phosphorylation-dependent manner. By using fluorescence resonance energy transfer between purified components labeled with fluorescent probes, we now show that the binding of synapsin I to actin is a rapid phenomenon. Binding of synapsin I
A non-radioactive automated method for DNA sequence determination.
Journal:J Biochem Biophys Methods
PubMed ID:3559035
A method and instrument for automated DNA sequencing without radioactivity have been developed. In spite of the success with radioactive labels there are drawbacks attached to the technique, such as hazards in the handling, storage and disposal of radioactive materials, and the considerable cost of the radiolabelled nucleoside triphosphates. In
Functional studies of the domains of talin.
Journal:J Cell Biol
PubMed ID:2110569
'The protein talin has two domains of approximately 200 and 47 kD, which can be cleaved apart by a variety of proteases. To examine the function of these two structural domains of talin, we have digested purified talin with a calcium-dependent protease and separated the resulting fragments chromatographically. Both fragments
Low molecular-weight G-actin binding proteins involved in the regulation of actin assembly during myofibrillogenesis.
Journal:Cell Struct Funct
PubMed ID:9113405
'We previously demonstrated that small G-actin binding proteins, cofilin, ADF and profilin, are involved in the actin dynamics during myofibrillogenesis (OBINATA, T. (1993). Int. Rev. Cytol., 143: 153-189.). To better understand how they are responsible for the regulation of actin assembly, the amounts of the actin-binding proteins were quantified by
Association of microinjected myosin and its subfragments with myofibrils in living muscle cells.
Journal:J Cell Biol
PubMed ID:3058721
'Purified skeletal muscle myosin was labeled with iodoacetamidofluorescein and microinjected into cultured chick myotubes. The fluorescent myosin analogue became incorporated within 10-15 min after injection, into either periodic (mean periodicity = 2.23 +/- 0.02 micron) bands or apparently continuous fibrillar structures. Comparison of rhodamine-labeled alpha-actinin with coinjected fluorescein-labeled myosin suggested