Alexa Fluor™ 568 C5 马来酰亚胺
Alexa Fluor&trade; 568 C<sub>5</sub> 马来酰亚胺
Invitrogen™

Alexa Fluor™ 568 C5 马来酰亚胺

Alexa Fluor™ 568 是一种明亮的橙红色荧光染料,其激发光谱非常适合于 Ar-Kr 混合气体激光器上的 568 nm 激光谱线。Alexa了解更多信息
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货号数量
A20341
又称 A-20341
1 mg
货号 A20341
又称 A-20341
价格(CNY)
5,856.00
Each
添加至购物车
数量:
1 mg
价格(CNY)
5,856.00
Each
添加至购物车
Alexa Fluor™ 568 是一种明亮的橙红色荧光染料,其激发光谱非常适合于 Ar-Kr 混合气体激光器上的 568 nm 激光谱线。Alexa Fluor™ 568 染料用于成像和流式细胞分析中稳定信号的生成,具有水溶性和 pH 值不敏感性(pH 值 4 至 pH 值 10)。除反应性染料制剂外,我们还提供可与多种抗体、肽、蛋白、示踪剂和扩增底物偶联并且针对细胞标记和检测进行优化的 Alexa Fluor™ 568 染料(了解更多信息)。

Alexa Fluor™ 568 的马来酰亚胺衍生物是将该染料与蛋白、寡核苷酸硫代磷酸盐或低分子量配体上的硫醇基团偶联的较常用工具。所得 Alexa Fluor™ 568 偶联物显示出比其他光谱相似荧光基团的偶联物更亮的荧光和更高的光稳定性。

关于该 AlexaFluor™ 马来酰亚胺的详细信息:

荧光基团标记:Alexa Fluor™ 568 染料
反应性基团:马来酰亚胺
反应性:蛋白质和配基上的硫醇基团、寡核苷酸硫代磷酸盐
偶联物的 Ex/Em:575/600 nm
消光系数:92,000 cm-1M-1
光谱类似染料:罗丹明红
分子量:880.92

典型偶联反应
在适当的缓冲液中,在 pH 值 7.0-7.5 下该蛋白浓度应为 50-100 µM(10-100 mM 磷酸盐、Tris 或 HEPES)。在此 pH 值范围内,蛋白硫醇基团亲核性强,在存在不计其数的蛋白胺(这些蛋白胺经过质子化,并且相对不具反应性)时,几乎仅与试剂反应。我们建议此时使用达到 DTT 或 TCEP 等还原剂摩尔量10倍的浓度还原所有二硫键。必须通过透析去除过量的 DTT,应在无氧条件下进行后续硫醇修饰,以防止二硫键再形成;在马来酰亚胺偶联之前使用 TCEP 时,无需采取这些预防措施。

Alexa Fluor™ 马来酰亚胺通常在即将使用前溶于高质量无水二甲亚砜 (DMSO) 中,浓度为1-10 mM,储备液应尽可能避光储存。通常,将这种储备液逐滴加入蛋白溶液中,同时搅拌,产生大约10-20摩尔试剂/摩尔蛋白,反应在室温下进行2小时,或在 4°C 下过夜避光进行。通过添加过量的谷胱甘肽、巯基乙醇或其他可溶性低分子量硫醇,可以消耗任何未反应的硫醇反应性试剂。

偶联物纯化
通常使用凝胶过滤柱(如 Sephadex™ G-25、BioGel™ P-30 或等效物)将标记抗体与游离 Alexa Fluor™ 染料分离。对于更大或更小的蛋白,选择具有适当分子量滤除点的凝胶过滤介质或通过透析纯化。我们提供了多种优化的纯化试剂盒,可用于不同量抗体偶联物:
0.5-1 mg 用抗体偶联物纯化试剂盒 (A33086)
20-50 µg 用抗体偶联物纯化试剂盒 (A33087)
50-100 µg 用抗体偶联物纯化试剂盒 (A33088)

了解关于蛋白和抗体标记的更多信息
我们提供一系列 Molecular Probes™ 抗体和蛋白标记试剂盒,旨在满足您的起始材料和实验设置需求。参见我们的抗体标记试剂盒或使用我们的标记化学选择工具进行其他选择。欲了解有关我们标记试剂盒的更多信息,请参阅 Molecular Probes™ 手册中第 1.2 节—蛋白和核酸标记试剂盒

我们还’可为您定制偶联物
如果您’无法在我们的在线目录中找到’想要的产品,我们还’可为您定制抗体或蛋白偶联物。我们的定制偶联服务是高效和保密的,我们保证我们的工作质量。我们经过ISO 9001:2000认证。
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600 nm
激发575 nm
标签或染料Alexa Fluor™ 568
产品类型染料
数量1 mg
反应一部分马来酰亚胺
运输条件室温
标签类型Alexa Fluor 染料
产品线Alexa Fluor
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 (5)

引用和文献
Abstract
The citrate carrier CitS probed by single-molecule fluorescence spectroscopy.
Authors:Kästner CN, Prummer M, Sick B, Renn A, Wild UP, Dimroth P
Journal:Biophys J
PubMed ID:12609868
'A prominent region of the Na(+)-dependent citrate carrier (CitS) from Klebsiella pneumoniae is the highly conserved loop X-XI, which contains a putative citrate binding site. To monitor potential conformational changes within this region by single-molecule fluorescence spectroscopy, the target cysteines C398 and C414 of the single-Cys mutants (CitS-sC398, CitS-sC414) were ... More
Receptor-mediated endocytosis of phosphodiester oligonucleotides in the HepG2 cell line: evidence for non-conventional intracellular trafficking.
Authors:de Diesbach P, N'Kuli F, Berens C, Sonveaux E, Monsigny M, Roche AC, Courtoy PJ
Journal:Nucleic Acids Res
PubMed ID:11917011
'Having identified an oligonucleotide (ON) receptor in the HepG2 cell line, we have re-examined here the kinetics of ON uptake, subcellular distribution and intracellular localisation in these cells, at concentrations relevant for the study of a receptor-dependent process. Kinetic parameters of ON endocytosis were comparable with those of the receptor-mediated ... More
Structure and conformational changes in the C-terminal domain of the beta2-adrenoceptor: insights from fluorescence resonance energy transfer studies.
Authors:Granier S, Kim S, Shafer AM, Ratnala VR, Fung JJ, Zare RN, Kobilka B,
Journal:J Biol Chem
PubMed ID:17347144
The C terminus of the beta(2)-adrenoceptor (AR) interacts with G protein-coupled receptor kinases and arrestins in an agonist-dependent manner, suggesting that conformational changes induced by ligands in the transmembrane domains are transmitted to the C terminus. We used fluorescence resonance energy transfer (FRET) to examine ligand-induced structural changes in the ... More
Efficiencies of fluorescence resonance energy transfer and contact-mediated quenching in oligonucleotide probes.
Authors:Marras SA, Kramer FR, Tyagi S
Journal:Nucleic Acids Res
PubMed ID:12409481
An important consideration in the design of oligonucleotide probes for homogeneous hybridization assays is the efficiency of energy transfer between the fluorophore and quencher used to label the probes. We have determined the efficiency of energy transfer for a large number of combinations of commonly used fluorophores and quenchers. We ... More
Arp2/3 ATP hydrolysis-catalysed branch dissociation is critical for endocytic force generation.
Authors:Martin AC, Welch MD, Drubin DG
Journal:Nat Cell Biol
PubMed ID:16862144
The Arp2/3 complex, which is crucial for actin-based motility, nucleates actin filaments and organizes them into y-branched networks. The Arp2 subunit has been shown to hydrolyse ATP, but the functional importance of Arp2/3 ATP hydrolysis is not known. Here, we analysed an Arp2 mutant in Saccharomyces cerevisiae that is defective ... More