Pierce™ EDC,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!
Pierce™ EDC,No-Weigh™ 规格
Thermo Scientific™

Pierce™ EDC,No-Weigh™ 规格

Thermo Scientific Pierce EDC 是羧基和胺反应性零长度交联剂。EDC 首先与羧基发生反应,形成胺反应性 O-酰基异脲中间体,该中间体可与氨基快速反应形成酰胺键,释放异脲副产物。中间体在水性溶液中不稳定,因此两步偶联程序依赖于 N-羟基琥珀酰亚胺了解更多信息
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货号数量
7714910 mg
A3539110 x 1 mg
229805 g
2298125 g
货号 77149
价格(CNY)
1,259.00
Each
添加至购物车
数量:
10 mg
请求批量或定制报价
价格(CNY)
1,259.00
Each
添加至购物车
Thermo Scientific Pierce EDC 是羧基和胺反应性零长度交联剂。EDC 首先与羧基发生反应,形成胺反应性 O-酰基异脲中间体,该中间体可与氨基快速反应形成酰胺键,释放异脲副产物。中间体在水性溶液中不稳定,因此两步偶联程序依赖于 N-羟基琥珀酰亚胺 (NHS) 进行稳定。如果不与胺发生反应,将导致中间体的水解、羧基的再生和 N-取代尿素的释放。副反应是形成 N-酰脲,通常仅限于位于蛋白疏水性区域的羧基。

Thermo Scientific No-Weigh 产品是可提供预分装规格的特殊试剂。预称重的包装可消除重复开瓶和关盖,从而防止随时间推移试剂反应性的降低和污染。对于这种规格,可每次使用一小瓶新鲜试剂,消除了对少量试剂进行称重的麻烦,并减少了对试剂稳定性的担忧。

EDC 的特点:

反应性基团碳二亚胺
反应靶标:活化羧基与氨基(伯胺)偶联
多种偶联策略—将 EDC 单独与靶标基团反应,或包括 NHS磺基-NHS,以提高反应效率或稳定活性中间体,用于后续胺类反应
中性键—在羧基和胺之间形成中性酰胺键
水溶性试剂—在水性生理缓冲液中直接加入进行反应
可溶性反应副产物—使用水或稀释酸洗涤即可轻松去除
高纯度结晶试剂—用于生成高质量、活化的衍生物

EDC 的属性
• 分子式:C8H17N3·HCl
• 分子量:191.7
•间隔臂长度:0 Å
• 货号:25952-53-8
• 反应基团:碳二亚胺
• 反应性:在 pH 值为 4.7–6.0(较优)的条件下与羧基形成活性中间体,然后中间体与伯胺发生反应

1-乙基-3[3-二甲基氨基丙基]碳二亚胺盐酸盐(EDC 或 EDAC)是一种零长度交联剂,用于将羧基偶联至伯胺。该交联剂已用于多种应用,如在肽合成中形成酰胺键、连接半抗原与载体蛋白形成免疫原、通过 5' 磷酸基标记核酸以及构建生物分子的胺反应性 NHS 酯。EDC 与羧基反应,形成胺反应性 O-酰基异脲中间体。如果这种中间体不遇到胺,它将水解并再生羧基。在存在 N-羟基磺基琥珀酰亚胺(磺基-NHS)的情况下,EDC 可用于将羧基转换为胺反应性磺基-NHS 酯。这是通过将 EDC 与含有羧基的分子混合并添加磺基-NHS 来实现的。

应用:
• 偶联肽和蛋白间的羧基与氨基基团
• 偶联半抗原与免疫原性载体蛋白(如将肽连接至 KLH
将肽抗原固定在亲和纯化抗体上
• 生成 NHS 活化、胺反应性标记化合物
• 交联蛋白与羧基包被的微珠或表面
• 使用胺反应性 Sulfo-NHS 酯活化纳米微粒
• 通过 5' 磷酸基进行 DNA 标记(参见 Tech Tip #30)

产品参考文献:
交联剂应用指南—检索本产品的近期参考文献
仅供科研使用。不可用于诊断程序。
规格
细胞渗透性
描述EDC
形式粉末
标记方法化学标记
分子量191.7
聚乙二醇化
产品线Pierce™
数量10 mg
反应一部分碳二亚胺
运输条件湿冰
溶解度
间隔臂长0.0 Å
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.

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.

What is the difference between the Thermo Scientific CarboLink (now Glycolink) and CarboxyLink Resins?

The CarboxyLink Resin is for immobilizing carboxyl-containing biomolecules after EDC activation. CarboLink Resin is hydrazide-activated and immobilizes glycoproteins. Carbolink has been replaced with glycolink immobilization kits and resins. Glycolink can also be used to immobilize steroids or other molecules containing ketones. Both resins are capable of coupling ligands via carboxylic acids using EDC (Cat. No. 22980). Both immobilization chemistries are available on UltraLink Resin as UltraLink Hydrazide (glycoproteins) and UltraLink DADPA (carboxyl) Resins.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

How do CarboxyLink and DADPA UltraLink Resins immobilize molecules?

These resins are derivatized with diaminodipropylamine (DADPA). DADPA has a terminal primary amine that enables covalent immobilization of peptides or other carboxyl-containing (-COOH) molecules. When incubated with the resin and the carbodiimide crosslinker EDC (included in the CarboxyLink Immobilization Kit), carboxyl-containing molecules become permanently attached to the resin by stable amide bonds. The immobilized molecules can then be used in affinity purification procedures. CarboxyLink/DADPA UltraLink Coupling Resins can also be used to immobilize other kinds of molecules using alternative amine-reactive crosslinking chemistries.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.