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Pyrene azide 2

Azides Pyrene Click chemistry
貨號 數量 價格 交貨時間
A2530 1 mg $110 現貨
B2530 5 mg $210 現貨
C2530 10 mg $310 現貨
D2530 25 mg $410 現貨
E2530 50 mg $695 現貨
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This pyrene azide is a derivative of pyreneacetic acid with triethyleneglycol (PEG3) linker.

An alternative pyrene azide with a shorter linker is also available. A detailed description of the fluorophore can be found there.

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sulfo-Cyanine5 amine

Sulfonated Cyanine5 amine derivative for the conjugation with electrophiles and enzymatic transamination labeling.

BDP 630/650 amine

BDP 630/650 is a far red emitting fluorophore for Cyanine5 channel. This fluorophore is based on BDP (borondipyrromethene) core, which provides high quantum yield and photostability. This is an amine derivative of this dye.
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sulfo-Cyanine5 dUTP

sulfo-Cyanine5 dUTP is a fluorescently labeled triphosphate used to enzymatically modify DNA with a sulfo-Cyanine5 fluorophore. The reagent contains a long linker arm, which makes incorporation highly efficient.
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General properties

Appearance: yellowish solid
Molecular weight: 416.47
CAS number: 1807512-45-3
Molecular formula: C24H24N4O3
Solubility: good solubility in chloroform, dichloromethane, moderate solubility in DMSO, DMF, acetonitrile
Quality control: NMR 1H (95%)
Storage conditions: Storage: 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light.
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產品規格

Spectral properties

Excitation/absorption maximum, nm: 343; 326; 313; 276; 265; 242; 234
Emission maximum, nm: 377; 397

產品引用

  1. Bednarczyk, M.; Peters, J.K.; Kasprzyk, R.; Starek, J.; Warminski, M.; Spiewla, T.; Mugridge, J.S.; Gross, J.D.; Jemielity, J.; Kowalska, J. Fluorescence-Based Activity Screening Assay Reveals Small Molecule Inhibitors of Vaccinia Virus mRNA Decapping Enzyme D9. ACS Chemical Biology, 2022, 17(6), 1460-1471. doi: 10.1021/acschembio.2c00049
  2. Wanat, P.; Walczak, S.; Wojtczak, B.A.; Nowakowska, M.; Jemielity, J.; Kowalska, J. Ethynyl, 2-Propynyl, and 3-Butynyl C-Phosphonate Analogues of Nucleoside Di- and Triphosphates: Synthesis and Reactivity in CuAAC. Organic Letters, 2015, 17(12), 3062–3065. doi: 10.1021/acs.orglett.5b01346
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