Search
Citações e referências (151)
Invitrogen™
Tetramethylrhodamine-5-Iodoacetamide Dihydroiodide (5-TMRIA), single isomer
The thiol-reactive tetramethylrhodamine-5-iodoacetamide dihydroiodide (5-TMRIA) can be used to can be used to create bright orange-red-fluorescent bioconjugates with excitation/emission maximaLeia mais
| Número do catálogo | Quantity |
|---|---|
| T6006 | 5 mg |
Número do catálogo T6006
Preço (BRL)
4.491,00
5 mg
Quantity:
5 mg
Preço (BRL)
4.491,00
5 mg
The thiol-reactive tetramethylrhodamine-5-iodoacetamide dihydroiodide (5-TMRIA) can be used to can be used to create bright orange-red-fluorescent bioconjugates with excitation/emission maxima ∼555/580.
For Research Use Only. Not for use in diagnostic procedures.
Especificações
Chemical ReactivityThiol
Emission580
Excitation555
Label or DyeRhodamine Isomers, TMR (Tetramethylrhodamine)
Product TypeTetramethylrhodamine-5-Iodoacetamide Dihydroiodide
Quantity5 mg
Reactive MoietyAlkyl Halide, Iodoacetamide
Shipping ConditionRoom Temperature
Label TypeClassic Dyes
Unit Size5 mg
Conteúdo e armazenamento
Store in freezer (-5 to -30°C) and protect from light.
Citações e referências (151)
Citações e referências
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