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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20°C. Desiccate
- 保质期:
2年
- 英文名:
Bis-sulfone Amine-5 g
- 库存:
100
- 供应商:
艾美捷科技
- CAS号:
查看datasheet
双砜胺-5 g,Bis-sulfone Amine-5 g,双砜胺-5 g,Bis-sulfone Amine-5 g
双砜胺-5 g-Bis-sulfone Amine-5 g
产品货号:CCT-1148-5G
产品规格:5g
双砜-PEG 4-DBCO是一种双烷基化标记试剂,能够将DBCO部分位点特异性掺入抗体上,形成明确的缀合物。该方法涉及两个步骤:(1)二硫键还原以释放两个半胱氨酸硫醇和(2)通过经由DBCO部分共价连接的三碳桥的双烷基化重新形成二硫键。在此过程中,蛋白质的不可逆变性,破坏其三级结构或其生物活性不会发生。文献中还报道了PEG与蛋白质上的多组氨酸标签(His标签)通过双烷基化试剂的共价、位点特异性偶联(参见选定参考文献章节)。

Bis-sulfone-PEG4-DBCO is a bis-alkylating labeling reagent that enables site-specific incorporation of DBCO moiety onto antibodies to form well-defined conjugates. Conjugates prepared with bis-sulfone reagents benefits from reduced heterogeneity and enhanced stability.DBCO reagents are the most commonly used substrates for strain-promoted copper-free azide-alkyne click chemistry reactions. DBCO compounds react with azide functionalized compounds or biomolecules without the need for a Cu(I) catalyst to result in a stable triazole linkage.

双砜胺-5 g-Bis-sulfone Amine-5 g-20°C. Desiccate
点击:双砜胺-5 g-Bis-sulfone Amine-5 g查看更详细产品说明,更多应用、储存、价格、货期等信息请垂询艾美捷科技有限公司。更多Vectorlabs公司Azides(Biotin-Azides)试剂、Bis-sulfone交联试剂、DBCO试剂、TCO试剂、Terminal Alkyne试剂、Tetrazine试剂、标记试剂盒以及分选用底物等。,请点击查看艾美捷特色产品中心。

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文献和实验Synthesis of Building Blocks and Oligonucleotides with {G}O6‐Alkyl‐O6{G} Cross‐Links
two methods for preparing oligonucleotides containing an O6 ?2??deoxyguanosine?alkyl?O6 ?2??deoxyguanosine interstrand cross?link by a solid?phase synthesis approach. Depending on the desired orientation of the cross?link in the DNA duplex, either a bis
Differences Between Biogenic Amine Detection by HPLC Methods Using OPA and Dansyl Derivates
an increasing search for trace compounds that can affect human health. Although they are present in fermented foods and beverages in low quantities, they exhibit interactions with normal human metabolism (e.g., having vasoactive or psychoactive properties
Modification of Alginate Using Mannuronan C-5-Epimerases
inversion of D-glucuronic acid into L-iduronic acid in dermatan ( 1 ) and heparin ( 2 ) synthesis and D-mannuronic acid (M) into L-guluronic acid (G) in alginates ( 3 ). The latter epimerization (Fig. 1 ), which is catalyzed by mannuronan C-5 epimerases
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