AFDye 488 Picolyl Azide

貨號
規(guī)格
價格
品牌
貨期
1276-1
1 mg
3800.0
ClickChemistryTools
現(xiàn)詢
1276-5
5 mg
11300.0
ClickChemistryTools
現(xiàn)詢
1276-25
25 mg
35900.0
ClickChemistryTools
現(xiàn)詢

Abs/Em Maxima: 494/517 nm

Extinction Coefficient: 73.000

Flow Cytometry Laser Line: 488 nm

Microscopy Laser Line: 488 nm

Spectrally Similar Dyes: Fluorescein, Alexa Fluor? 488, CF? 488A, DyLight? 488, Atto? 488

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ZDye? 488 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? 488 is structurally identical to Alexa Fluor? 488. Its absorption/emission spectra is a perfect match to spectra of many other fluorescent dyes based on sulfonated rhodamine 110 core, including DyLight? 488, Alexa Fluor? 488, and CF? 488A.

分子量
763.69 (protonated)
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. Morral, C., et al. (2020). Protocol for Efficient Protein Synthesis Detection by Click Chemistry in Colorectal Cancer Patient-Derived Organoids Grown In Vitro. STAR Protocols, Volume 1, 2 [ScienceDirect]

2. Uchiyama, J., et al. (2020). Quantitative nascent proteome profiling by dual pulse labeling with O-propargyl-puromycin and stable isotope labeled amino acids. The Journal of Biochemistry, 10, 1093. [Oxford Academic]

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

4. 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]

5. 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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