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貨物所在地:
上海上海市
產(chǎn)地:
美國
更新時間:
2023-11-26 21:00:18
有效期:
2023年11月26日 -- 2024年5月26日
已獲點擊:
1282
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產(chǎn)品特點
Highly selective, low background labeling
Rapid and quantitative labeling
Multiple fluorophore selection for multicolor imaging

詳細介紹

Click Chemistry is a new approach to rapidly and selectively react ("click") a pair of functional groups with each other in mild, aqueous conditions. Click Chemistry reactions can be categorized into two separate groups: (1) Cu(I)-catalyzed Azide-Alkyne Click Chemistry reaction (CuAAC); (2) Strain-promoted Azide-Alkyne Click Chemistry reaction (SPAAC).
Biomolecules that have been functionalized with a CLICK moiety (e.g. a terminal Alkyne or Azide) can be detected by labeling with a compatible CLICKable fluorescent dye (e.g. a fluorescent Azide or Alkyne) that allows the subsequent visualization by fluorescence spectroscopy. Applied BioProbes has developed a series of CLICKable biotin and fluorescent dyes for efficient “click” labeling of biomolecules.

 
Figure 1. Click chemistry labeling

Standard CuAAC reactions
Azides and alkynes can be used interchangeably in standard CuAAC reactions, so either one can serve as the tagged substrate or be labeled for the detection step. Some biomolecules are sensitive to the amount of copper used to catalyze standard click reactions. In particular, proteins such as GFP and R-PE exhibit reduced fluorescence and nucleic acids can be denatured by a high-copper environment.

Picolyl azides for low-copper reactions
Picolyl azide reagents enable researchers to perform copper-catalyzed click reactions with compounds that are sensitive to copper, while retaining all of the benefits of the original azide/alkyne click reaction. Picolyl azide only need much lower copper concentration than standard click reactions to protect against undesired copper side reactions with proteins (e.g., GFP, RPE), nucleic acids (e.g., RNA, oligos), and even small molecules (e.g., phalloidin). Additionally the picolyl azides can be used to increase sensitivity or accelerate the reactions by using the original copper-catalyzed reaction conditions.

DBCO alkynes for copper-free reactions
DBCO reagents can be used to perform click reactions with azide-modified targets without the use of heavy metal catalysis. DBCO reactions are ideal for surface labeling of live cells and also minimize damage to fluorescent proteins like GFP or R-PE.

CLICKable Biotin and Fluorescent Dye Selection Guide

LabelAlkyneAzidePicolyl azideDBCO
BiotinC303C304C325 C330
5-FAMC305C306  
5-TAMRAC307C308  
Texas RedC309C310  
Cy3C311C312C337C335
Cy5C313C314C338C336
Andy Fluor™ 350C315C316  
Andy Fluor™ 488C317C318C326C331
Andy Fluor™ 555C319C320C327C332
Andy Fluor™ 594C321C322C328C333
Andy Fluor™ 647C323C324C329C334

 

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