5(6)-SFX(6-(荧光素-5-(和-6)-甲酰胺) 己酸琥珀酰亚胺酯),混合异构体
5(6)-SFX(6-(荧光素-5-(和-6)-甲酰胺) 己酸琥珀酰亚胺酯),混合异构体
Invitrogen™

5(6)-SFX(6-(荧光素-5-(和-6)-甲酰胺) 己酸琥珀酰亚胺酯),混合异构体

荧光素是一种常见的绿色荧光衍生化试剂,而琥珀酰亚胺酯经常用于标记蛋白、胺修饰的寡核苷酸及其他含胺分子的伯胺 (R-NH2)。该“SFX”琥珀酰亚胺酯包含荧光基团和反应性基团之间的七原子氨基 - 己酰基间隔。该间隔可将荧光基团与其偶联的生物分子分离,可能减少通常在偶联时发生的淬灭作用。可利用标准 FITC了解更多信息
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货号数量
F2181
又称 F-2181
10 mg
货号 F2181
又称 F-2181
价格(CNY)
3,200.00
Each
添加至购物车
数量:
10 mg
价格(CNY)
3,200.00
Each
添加至购物车
荧光素是一种常见的绿色荧光衍生化试剂,而琥珀酰亚胺酯经常用于标记蛋白、胺修饰的寡核苷酸及其他含胺分子的伯胺 (R-NH2)。该“SFX”琥珀酰亚胺酯包含荧光基团和反应性基团之间的七原子氨基 - 己酰基间隔。该间隔可将荧光基团与其偶联的生物分子分离,可能减少通常在偶联时发生的淬灭作用。可利用标准 FITC 或 GFP 滤光片组检测产生的荧光素偶联物。荧光素染料及其偶联物具有相对较高的光漂白速率和 pH 值敏感的荧光。Alexa Fluor™ 488 和 Oregon Green™ 488 是替代染料,其光谱可模拟荧光素的光谱,更具光稳定性,在生理 pH 值范围内几乎无 pH 值敏感性。

规格:

• 荧光基团标记:荧光素

• 反应性基团:琥珀酰亚胺酯

• 反应性:蛋白和配体上的伯胺、胺修饰的寡核苷酸

• 分子量:586

• 消光系数:74,000 cm-1M-1

• 偶联物的激发/发射波长:494/520 nm

• 光谱相似染料:Alexa Fluor™ 488,GFP

典型偶联反应

胺反应性试剂可与几乎任何蛋白或肽偶联;提供的方案针对 IgG 抗体进行了优化。您可以针对任何量的蛋白按比例缩放反应,但为了获得最佳结果,蛋白的浓度应至少为 2 mg/mL。我们建议使用 3 种不同摩尔比的反应性试剂对蛋白进行 3 种不同程度的标记。

荧光素琥珀酰亚胺酯通常溶于高质量的无水二甲基甲酰胺 (DMF) 或二甲亚砜 (DMSO) 中,并在 0.1–0.2 M 碳酸氢钠缓冲液(pH 值 8.3)中于室温下进行反应,持续 1 小时。由于末端胺的 pKa 低于赖氨酸 ε-氨基基团的 pKa,因此您可以使用接近中性 pH 值的缓冲液对胺末端进行更具选择性的标记。

偶联物纯化

通常使用凝胶过滤柱(如 Sephadex™ G-25、BioGel™ P-30 或等效产品)将标记抗体与游离染料分离。对于更大或更小的蛋白,选择具有适当截留分子量的凝胶过滤介质或通过透析纯化。

替代包装

荧光素的混合异构体胺反应性琥珀酰亚胺酯也以 10 x 1 mg 单位规格 (F6129)、单异构体 (F6106) 和间隔比 SFX 间隔更具亲水性的形式 (F6130),以及用于标记蛋白和核酸的大量试剂盒(用于标记蛋白和核酸的活性酯和试剂盒—表 1.2)的形式提供。
仅供科研使用。不可用于诊断程序。
规格
化学反应性
发射520
激发494
标签或染料FITC(荧光素)
数量10 mg
反应一部分活性酯、琥珀酰亚胺酯
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 (29)

引用和文献
Abstract
Macromolecular accessibility of fluorescent taxoids bound at a paclitaxel binding site in the microtubule surface.
Authors:Díaz JF, Barasoain I, Souto AA, Amat-Guerri F, Andreu JM
Journal:J Biol Chem
PubMed ID:15550392
'The macromolecular accessibility of the paclitaxel binding site in microtubules has been investigated using a fluorescent taxoid and antibodies against fluorescein, which cannot diffuse into the microtubule lumen. The formation of a specific ternary complex of microtubules, Hexaflutax (7-O-{N-[6-(fluorescein-4''-carboxamido)-n-hexanoyl]-l-alanyl}paclitaxel) and 4-4-20 IgG (a monoclonal antibody against fluorescein) has been observed ... More
High-affinity binding of the Drosophila Numb phosphotyrosine-binding domain to peptides containing a Gly-Pro-(p)Tyr motif.
Authors:Li SC, Songyang Z, Vincent SJ, Zwahlen C, Wiley S, Cantley L, Kay LE, Forman-Kay J, Pawson T
Journal:Proc Natl Acad Sci U S A
PubMed ID:9207069
'The phosphotyrosine-binding (PTB) domain is a recently identified protein module that has been characterized as binding to phosphopeptides containing an NPXpY motif (X = any amino acid). We describe here a novel peptide sequence recognized by the PTB domain from Drosophila Numb (dNumb), a protein involved in cell fate determination ... More
The ligand for osteoprotegerin (OPGL) directly activates mature osteoclasts.
Authors:Burgess TL, Qian Y, Kaufman S, Ring BD, Van G, Capparelli C, Kelley M, Hsu H, Boyle WJ, Dunstan CR, Hu S, Lacey DL
Journal:J Cell Biol
PubMed ID:10225954
'Osteoprotegerin (OPG) and OPG-ligand (OPGL) potently inhibit and stimulate, respectively, osteoclast differentiation (Simonet, W.S., D.L. Lacey, C.R. Dunstan, M. Kelley, M.-S. Chang, R. Luethy, H.Q. Nguyen, S. Wooden, L. Bennett, T. Boone, et al. 1997. Cell. 89:309-319; Lacey, D.L., E. Timms, H.-L. Tan, M.J. Kelley, C.R. Dunstan, T. Burgess, R. ... More
Evolution of peptides that modulate the spectral qualities of bound, small-molecule fluorophores.
Authors:Rozinov MN, Nolan GP
Journal:Chem Biol
PubMed ID:9862799
'BACKGROUND: Fluorophore dyes are used extensively in biomedical research to sensitively assay cellular constituents and physiology. We have created, as proof of principle, fluorophore dye binding peptides that could have applications in fluorescent dye-based approaches in vitro and in vivo. RESULTS: A panel of Texas red, Rhodamine red, Oregon green ... More
Mutations in the P. falciparum digestive vacuole transmembrane protein PfCRT and evidence for their role in chloroquine resistance.
Authors:Fidock DA, Nomura T, Talley AK, Cooper RA, Dzekunov SM, Ferdig MT, Ursos LM, Sidhu AB, Naudé B, Deitsch KW, Su XZ, Wootton JC, Roepe PD, Wellems TE
Journal:Mol Cell
PubMed ID:11090624
'The determinant of verapamil-reversible chloroquine resistance (CQR) in a Plasmodium falciparum genetic cross maps to a 36 kb segment of chromosome 7. This segment harbors a 13-exon gene, pfcrt, having point mutations that associate completely with CQR in parasite lines from Asia, Africa, and South America. These data, transfection results, ... More