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						31952518
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						DBCO-Amine	
					
					
					| Catalog # | Pkg Size | Price | Quantity | Shopping Cart | 
|---|---|---|---|---|
| R-CD-011 | 25mg | ¥ 750 | 加入购物车 | |
| R-CD-011 | 100mg | ¥ 1800 | 加入购物车 | |
| R-CD-011 | 500mg | ¥ 5500 | 加入购物车 | |
							结构式							
						
						 
	
                         						| 外观 | Slightly yellow to slightly crystalline | 
| 分子量 | 276.33 | 
| 溶解度 | DMSO, DMF, DCM, THF, Chloroform | 
| CAS号 | 1255942-06-3 | 
| 质量控制 | 95% | 
| 储存条件 | -20°C | 
| 保存时间 | 1 year | 
| 其他信息 | N/A | 
							DBCO-Amine is a simple DBCO-containing building block used to derivatize carboxyl groups in the presence of activators (e.g. EDC, or DCC) or activated esters (e.g. NHS esters) with DBCO moiety through a stable amide bond. A short spacer arm adds minimal mass to modified molecules (273.3 daltons).
						
						
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						| DBCO-C6-NHS Ester | DBCO-C6-NHS Ester is an amine-reactive building block used for modification of amine-containing molecule in organic media. | 
| DBCO-NHS Ester | DBCO-NHS Ester is an amine-reactive building block used for modification of amine-containing molecule in organic media. | 
| DBCO-Sulfo-NHS Ester | DBCO-Sulfo-NHS Ester is water-soluble reagent that enables simple and efficient labeling of antibodies, proteins and any other primary amine-containing macromolecules with DBCO moiety in 100% aqueous buffers. | 
| DBCO-PEG4-NHS Ester | DBCO-PEG4-NHS Ester reacts specifically and efficiently with a primary amine (e.g., side chain of lysine residues or aminosilane-coated surfaces) at pH 7-9 to form a covalent bond. | 
| DBCO-PEG5-NHS Ester | DBCO-PEG5-NHS Ester reacts specifically and efficiently with a primary amine (e.g., side chain of lysine residues or aminosilane-coated surfaces) at pH 7-9 to form a covalent bond. | 
| DBCO-PEG13-NHS Ester | DBCO-PEG13-NHS Ester reacts specifically and efficiently with a primary amine (e.g., side chain of lysine residues or aminosilane-coated surfaces) at pH 7-9 to form a covalent bond. The hydrophilic polyethylene glycol (PEG) spacer arm imparts water solubility and provides a long and flexible connection that minimizes steric hindrance involved with ligation to complementary azide-containing molecules. | 
 
	
				
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