AFDye 405 Picolyl Azide

貨號
規(guī)格
價格
品牌
貨期
1308-1
1 mg
3580.0
ClickChemistryTools
現(xiàn)詢
1308-5
5 mg
10900.0
ClickChemistryTools
現(xiàn)詢
1308-25
25 mg
29900.0
ClickChemistryTools
現(xiàn)詢

Abs/Em Maxima: 402/424 nm

Extinction Coefficient: 35,000

Flow Cytometry Laser Line: 405 nm

Microscopy Laser Line: 405 nm

Spectrally Similar Dyes: Alexa Fluor? 405, CF? 405, Cascade Blue?, DyLight? 405

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AZDye? 405 Picolyl Azide is an advanced fluorescent probe that incorporates a copper-chelating motif to raise the effective concentration of Cu(I) at the reaction site to boost the efficiency of the CuAAC reaction, resulting in a faster and more biocompatible CuAAC labeling. Up to 40-fold increase of signal intensity, compared to conventional azides, was reported (see Selected References).

In addition, the use picolyl azides instead of conventional azides allows for at least a tenfold reduction in the concentration of the copper catalyst without sacrificing the efficiency of labeling, significantly improving biocompatibility of CuAAC labeling protocol.

In summary, the introduction of a copper-chelating motif into azide probe leads to a substantial increase in the sensitivity and reduced cell toxicity of CuAAC detection alkyne-tagged biomolecules. This will be of special value for the detection of low abundance targets or living system imaging.

AZDye? 405 is structurally similar and spectrally is almost identical to DyLight? 405, Alexa Fluor? 405, CF? 405S Dye, or any other sulfonated pyrene based fluorescent dyes.

分子量
718.68 (protonated) 1022.26 (triethylammonium salt)
分子式
N/A
CAS
N/A
溶(解)度
Water, DMSO, DMF
純度
>95% (HPLC)
外觀
Yellow solid
儲存環(huán)境
-20°C. Desiccate
運輸條件
Ambient temperature

1. Jiang, H., et al. (2014). Monitoring Dynamic Glycosylation in Vivo Using Supersensitive Click Chemistry. Bioconjugate Chem.,, 25, 698-706. [PubMed]

2. Uttamapinant, C., et al. (2012). Fast, Cell-Compatible Click Chemistry with Copper-Chelating Azides for Biomolecular Labeling. Angew. Chem. Int. Ed,., 51, 5852-56. [PubMed]

3. Gaebler, A.,et al. (2016). A highly sensitive protocol for microscopy of alkyne lipids and fluorescently tagged or immunostained proteins. J. Lipid. Res., 57, 1934-47. [PubMed]


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