AFDye 430 Picolyl Azide

貨號(hào)
規(guī)格
價(jià)格
品牌
貨期
1272-1
1 mg
3180.0
ClickChemistryTools
現(xiàn)詢(xún)
1272-5
5 mg
9900.0
ClickChemistryTools
現(xiàn)詢(xún)
1272-25
25 mg
29900.0
ClickChemistryTools
現(xiàn)詢(xún)

Abs/Em Maxima: 430/537 nm

Extinction Coefficient: 15,000

Spectrally Similar Dyes: Alexa Fluor? 430, CF? 430

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AZDye? 430 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? 430 is structurally identical to Alexa Fluor? 430. Its absorption/emission spectra is a perfect match to spectra of many other structurally similar dyes, including Alexa Fluor? 430 and CF?430 Dye.

分子量
705.71 (protonated)
分子式
N/A
CAS
N/A
溶(解)度
Water, DMSO, DMF
純度
>95% (HPLC)
外觀
Yellow solid
儲(chǔ)存環(huán)境
-20°C. Desiccate
運(yùn)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]


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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