Sulfo-NHS(N-羟基磺基琥珀酰亚胺),No-Weigh™ 规格
Invitrogen17万+抗体限时买二赠一,靶点广,灵活用!
Invitrogen17万+抗体限时买二赠一,靶点广,灵活用!
Sulfo-NHS(N-羟基磺基琥珀酰亚胺),No-Weigh™ 规格
Sulfo-NHS(N-羟基磺基琥珀酰亚胺),No-Weigh™ 规格
Sulfo-NHS(N-羟基磺基琥珀酰亚胺),No-Weigh™ 规格
Sulfo-NHS(N-羟基磺基琥珀酰亚胺),No-Weigh™ 规格
Thermo Scientific™

Sulfo-NHS(N-羟基磺基琥珀酰亚胺),No-Weigh™ 规格

Thermo Scientific Pierce Sulfo-NHS是一款用于将羧基转换为氨基反应性NHS酯的化学修饰试剂,适用于生物偶联、交联、标记和固定等操作。Sulfo-NHS的特点:• Sulfo-NHS提高EDC介导的偶联效率• 能够利用任何含羧基分子形成氨基反应性NHS酯或Sulfo-NHS酯• Sulfo-NHS衍生物通常直接溶于水了解更多信息
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货号数量
245255 g
24510500 mg
A3926910 x 2 mg
货号 24525
价格(CNY)
28,197.00
Each
添加至购物车
数量:
5 g
请求批量或定制报价
价格(CNY)
28,197.00
Each
添加至购物车
Thermo Scientific Pierce Sulfo-NHS是一款用于将羧基转换为氨基反应性NHS酯的化学修饰试剂,适用于生物偶联、交联、标记和固定等操作。

Sulfo-NHS的特点:

• Sulfo-NHS提高EDC介导的偶联效率
• 能够利用任何含羧基分子形成氨基反应性NHS酯或Sulfo-NHS酯
• Sulfo-NHS衍生物通常直接溶于水(可直接加入生理缓冲液中),不可穿透细胞膜(可用于标记细胞表面)
• 高纯度的晶体Sulfo-NHS可用于生成高品质活化衍生物

Sulfo-NHS(N-羟基琥珀酰亚胺)能够控制和修饰碳二亚胺交联反应,包括活化羧酸根(—COOH)以偶联伯胺基(—NH2)。通过将Sulfo-NHS与一种含羧基分子及一种脱水试剂(如碳二亚胺EDC(EDAC))混合,可以方便地合成相关衍生物。该方法是制备许多类型蛋白标记试剂的基础,包括氨基反应性荧光染料、生物素亲和标签和聚乙二醇化化合物。

应用:
• 提高EDC偶联反应效率
• 将羧基转化为氨基反应性Sulfo-NHS酯
• 在蛋白与羧基包被微珠或表面之间实现高效交联
• 使用氨基反应性Sulfo-NHS酯活化纳米颗粒

Sulfo-NHS的规格:
我们按照最高标准生产N-羟基琥珀酰亚胺以获得最特异的生物偶联物,进而确保数据的完整性,并为您提供最高水平的实验一致性。每一批次的Sulfo-NHS均经过测试,符合以下标准:

纯度—定量NMR检测纯度≥95%(交联剂纯度的最高标准)
每批次的平均纯度高于99%
可溶性—2 mg/mL下溶解于去离子水,形成清澈的无色溶液
鉴别检测—IR扫描只显示N-羟基琥珀酰亚胺的特性峰值

产品参考文献:
交联剂应用指南— 搜索本品最新参考文献

相关资源:

交联综述
交联化学原理

相关产品:
EDC(碳二亚胺交联剂)
生物偶联技术(书籍)
交联剂一览(选择指南)
NHS激活生物素标记试剂
NHS激活荧光标记试剂
NHS激活琼脂糖树脂
NHS激活磁珠
仅供科研使用。不可用于诊断程序。
规格
细胞渗透性
描述Sulfo-NHS
形式粉末
标记方法化学标记
分子量217.13
聚乙二醇化
产品线Pierce™
数量5 g
反应一部分碳二亚胺
运输条件环境
溶解度
水溶性
化学反应性胺基 - 羧基
可裂解
交联剂类型异型双功能团试剂
产品规格标准品,一次性使用,优级
产品类型交联剂
间隔子短 (<10 Å)
Unit SizeEach

常见问题解答 (FAQ)

Can NHS and EDC stock solutions be made for long-term storage before use?

No. EDC is very unstable in aqueous environments and must be dissolved immediately before use. NHS and Sulfo-NHS are relatively stable in solution but best results are obtained when they are dissolved immediately before use. Store these compounds desiccated at 4°C.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Are there any substances that interfere with NHS reactions?

Yes. Except for the intended targets, reactions must not contain carboxyl or amine compounds. Thus, Tris, glycine, lysine, ethanolamine or other amine- containing buffers must be avoided.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What is the difference between NHS and Sulfo-NHS?

Sulfo-NHS is the sulfonate sodium salt of NHS; it is water-soluble, but not membrane-permeable. NHS is membrane-permeable and water-soluble. NHS is soluble in organic solvents, as is Sulfo-NHS to a lesser extent. Because NHS is a leaving group in reactions with primary amines, the final conjugation product resulting from NHS and Sulfo-NHS reactions is identical. Sulfo-NHS is chosen for its ability to confer better solubility to the activated compound and/or to control its membrane permeability.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

How are NHS and Sulfo-NHS used?

These compounds are used to modify a carboxyl group to form an amine-reactive ester. This is accomplished by mixing NHS with a carboxyl-containing molecule and the carbodiimide EDC (Cat. No. 22980, 22981, 77149, A35391). EDC causes a dehydration reaction between the carboxyl and the NHS hydroxyl group, giving rise to an NHS-ester-activated molecule. The activated molecule can then be reacted spontaneously with a primary amine-containing molecule. Although the carboxyl-molecules can be made to react directly with amines using EDC, the reaction is much more efficient with NHS because a stable intermediate is created. In fact, molecules that are activated as NHS esters can be dried and stored for later reaction to amine-containing targets.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What are NHS and Sulfo-NHS used for?

These compounds are used in conjunction with the crosslinker EDC (Cat. No. 22980, 22981, 77149, A35391) to synthesize amine-reactive labeling reagents, crosslinkers and conjugation compounds. Any compound containing a carboxylic acid (-COOH), such as a protein, or biotin or peptide, can be activated with NHS or Sulfo-NHS to form an NHS ester that will spontaneously react to form covalent amide linkages with proteins and other molecules that contain primary amines (-NH2).

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.