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Sulfo DBCO-Amine
| Catalog # | Pkg Size | Price | Quantity | Shopping Cart |
|---|---|---|---|---|
| R-CD-013 | 25mg | ￥ 2500 | 加入購物車 | |
| R-CD-013 | 100mg | ￥ 5500 | 加入購物車 | |
Datasheet
MSDS
COA
結構式
| 外觀 | Slightly yellow to slightly grey crystalline |
| 分子量 | 427.47 |
| 溶解度 | Water, DMSO, DMF |
| CAS號 | N/A |
| 質量控制 | 95% |
| 儲存條件 | -20°C |
| 保存時間 | 1 year |
| 其他信息 | N/A |
Sulfo DBCO-Amine is a water-soluble building block used to derivatize carboxyl-containing molecules or activated esters (e.g. NHS esters) with DBCO moiety through a stable amide bond. The hydrophilic sulfonated spacer arm greatly improves water solubility of DBCO derivatized molecules, in many cases making it completely soluble in aqueous media. A short spacer arm adds minimal mass to modified molecules.
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相關產品
| 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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