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PC DBCO-NHS Ester
| Catalog # | Pkg Size | Price | Quantity | Shopping Cart |
|---|---|---|---|---|
| R-CD-007 | 10mg | ￥ 1520 | 加入購物車 | |
| R-CD-007 | 25mg | ￥ 3120 | 加入購物車 | |
| R-CD-007 | 100mg | ￥ 8784 | 加入購物車 | |
Datasheet
MSDS
COA
結(jié)構(gòu)式
| 外觀 | Yellow amorphous solid |
| 分子量 | 945.96 |
| 溶解度 | DMF, DMSO, DCM, THF, Chloroform |
| CAS號 | N/A |
| 質(zhì)量控制 | 95% |
| 儲存條件 | -20°C |
| 保存時間 | 1 year |
| 其他信息 | N/A |
Photocleavable DBCO-NHS ester reagent contains an amine reactive group linked to DBCO moiety through a spacer arm containing a photocleavable moiety. Molecules jointed by the copper-free click reaction can be efficiently photoreleased, typically >90% in 5-25 minutes using an inexpensive, near-UV, low intensity lamp (e.g. 365 nm lamp at 1-5 mW/cm2).
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相關(guān)產(chǎn)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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