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引用和文献 (6)
Invitrogen™
QSY™ 7 C5-马来酰亚胺
QSY™ 7 C5-马来酰亚胺是一种非荧光受体染料（最大吸收波长 ∼560 nm），用于通过硫醇修饰制备 FRET 探针。了解更多信息
| 货号 | 数量 |
|---|---|
| Q10257 | 5 mg |
货号 Q10257
价格（CNY)
5,463.00
Each
数量:
5 mg
价格（CNY)
5,463.00
Each
QSY™ 7 C5-马来酰亚胺是一种非荧光受体染料（最大吸收波长 ∼560 nm），用于通过硫醇修饰制备 FRET 探针。
仅供科研使用。不可用于诊断程序。
规格
化学反应性硫醇
标签或染料QSY™ 7
产品类型马来酰亚胺
数量5 mg
反应一部分马来酰亚胺
运输条件室温
标签类型淬灭染料
产品线QSY
Unit SizeEach
内容与储存
储存在冰箱中 (-5 - -30°C) 并避光。
引用和文献 (6)
引用和文献
Abstract
Asymmetric amino acid activation by class II histidyl-tRNA synthetase from Escherichia coli.
Journal:J Biol Chem
PubMed ID:19487703
'Aminoacyl-tRNA synthetases (ARSs) join amino acids to their cognate tRNAs to initiate protein synthesis. Class II ARS possess a unique catalytic domain fold, possess active site signature sequences, and are dimers or tetramers. The dimeric class I enzymes, notably TyrRS, exhibit half-of-sites reactivity, but its mechanistic basis is unclear. In
Quantum dot-based multiplexed fluorescence resonance energy transfer.
Journal:J Am Chem Soc
PubMed ID:16366574
We demonstrate the use of luminescent quantum dots (QDs) conjugated to dye-labeled protein acceptors for nonradiative energy transfer in a multiplexed format. Two configurations were explored: (1) a single color QD interacting with multiple distinct acceptors and (2) multiple donor populations interacting with one type of acceptor. In both cases,
Visualizing the distribution and transport of mRNAs in living cells.
Journal:Proc Natl Acad Sci U S A
PubMed ID:14583593
We have visualized the movements of native mRNAs in living cells. Using nuclease-resistant molecular beacons, we imaged the transport and localization of oskar mRNA in Drosophila melanogaster oocytes. When the localization pattern was altered by genetic manipulation of the mRNA's 3' untranslated region, or by chemical perturbation of the intracellular
Resonance energy transfer for assessing the molecular integrity of proteins for local delivery.
Journal:Biotechnol Bioeng
PubMed ID:14755558
It remains unclear whether the limitations to the therapeutic potential of angiogenic growth factors stem from pharmacokinetic concerns related to inadequate delivery or from a reduced sensitivity of target tissues. Here, we report a novel method using resonance energy transfer to assess the molecular integrity of proteins after local delivery.
Docking and rolling, a model of how the mitotic motor Eg5 works.
Journal:J Biol Chem
PubMed ID:16115880
Whereas kinesin I is designed to transport cargoes long distances in isolation, a closely related kinesin motor, Eg5, is designed to generate a sustained opposing force necessary for proper mitotic spindle formation. Do the very different roles for these evolutionarily related motors translate into differences in how they generate movement?