946123-12-2,AF 343 (Coumarin) X NHS ester,可以作为一种荧光标记试剂

英文名:AF 343 (Coumarin) X NHS ester

中文名:AF 343 (香豆素) X活性酯

CAS号:946123-12-2

Molecular formula:C26H29N3O7

Molecular weight:495.52

Purity:95%+

Appearance:solid/powder

Matters for use:

It is sensitive to light and temperature. In order to use the reagent effectively, the material should always be kept in a low temperature dry condition, away from light, and avoid frequent thawing and freezing.

storage conditions:

Store at - 20 ℃ as much as possible. If conditions permit, the material can be treated under inert gas to obtain better stability of the reagent.

Packing specification:10mg、25mg、50mg

结构式:

产品介绍:

AF 343 (Coumarin) X NHS Ester,也被称为AF 343 (香豆素) X活性酯,是一种重要的香豆素类荧光染料,其CAS号为946123-12-2。这种染料因其独特的荧光特性和广泛的科研应用价值,在生物学和化学等多个领域得到了广泛应用。本文将详细介绍AF 343 (Coumarin) X NHS Ester的基本性质、反应活性、应用领域以及注意事项。

AF 343 (Coumarin) X NHS Ester是一种胺反应性的NHS酯,其独特的结构特点使其能够与多种分子发生反应。这种染料在荧光团和反应基团之间含有氨基己酰基连接体,这种连接体不仅提供了更好的溶解性,还在荧光团和被标记的目标分子之间提供了空间分离,从而增强了染料的稳定性和反应活性。特别地,AF 343 (Coumarin) X NHS Ester能够与荧光素(FAM)形成FRET对,这种特性使得它在荧光共振能量转移(FRET)实验中具有重要的应用价值。

同类型相关产品:

AF350 C5 Maleimide,AF350 C5马来酰亚胺

AF532 C5 Maleimide,AF532 C5马来酰亚胺

AF594 C5 Maleimide,AF594 C5马来酰亚胺

AF568 carboxylic acid,AF568 羧基

AF568 NHS ester,AF568 琥珀酰亚胺酯

AF488 alkyne, 5-isomer,AF488 炔基, 5-异构体

AF488 DBCO, 5-isomer,AF488 二苯基环辛炔, 5-异构体

AF488 C5 Maleimide,AF488 C5马来酰亚胺

AF350 NHS Ester,AF350琥珀酰亚胺酯

AF532 NHS Ester,AF532琥珀酰亚胺酯

AF488 Hydroxylamine,AF488 羟胺

(文章资料汇总来源于:陕西新研博美生物科技小编木木)

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润色下面英文:The controlled drug delivery systems, due to their precise control of drug release in spatiotemporal level triggered by specific stimulating factors and advantages such as higher utilization ratio of drug, less side-effects to normal tissues and so forth, provide a new strategy for the precise treatment of many serious diseases, especially tumors. The materials that constitute the controlled drug delivery systems are called “smart materials” and they can respond to the stimuli of some internal (pH, redox, enzymes, etc.) or external (temperature, electrical/magnetic, ultrasonic and optical, etc.) environments. Before and after the response to the specific stimulus, the composition or conformational of smart materials will be changed, damaging the original balance of the delivery systems and releasing the drug from the delivery systems. Amongst them, the photo-controlled drug delivery systems, which display drug release controlled by light, demonstrated extensive potential applications, and received wide attention from researchers. In recent years, photo-controlled drug delivery systems based on different photo-responsive groups have been designed and developed for precise photo-controlled release of drugs. Herein, in this review, we introduced four photo-responsive groups including photocleavage groups, photoisomerization groups, photo-induced rearrangement groups and photocrosslinking groups, and their different photo-responsive mechanisms. Firstly, the photocleavage groups represented by O-nitrobenzyl are able to absorb the energy of the photons, inducing the cleavage of some specific covalent bonds. Secondly, azobenzenes, as a kind of photoisomerization groups, are able to convert reversibly between the apolar trans form and the polar cis form upon different light irradiation. Thirdly, 2-diazo-1,2-naphthoquinone as the representative of the photo-induced rearrangement groups will absorb specific photon energy, carrying out Wolff rearrangement reaction. Finally, coumarin is a promising category photocrosslinking groups that can undergo [2+2] cycloaddition reactions under light irradiation. The research progress of photo-controlled drug delivery systems based on different photo-responsive mechanisms were mainly reviewed. Additionally, the existing problems and the future research perspectives of photo-controlled drug delivery systems were proposed.
02-06
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