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Cyanine 3-UTP (enhanced)

更新時間：2022-01-27

簡要描述：

Cyanine 3-UTP (Enhanced) can replace UTP as a substrate for T7 RNA polymerase in labeling systems that generate labeled probes through in vitro transcription. Probes generated by these methods are……

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Cyanine 3-UTP (Enhanced) can replace UTP as a substrate for T7 RNA polymerase in labeling systems that generate labeled probes through in vitro transcription. Probes generated by these methods are suitable for multicolor fluorescence analysis, specifically dual-color expression arrays in conjunction with cyanine 3-UTP .


Product Details

Alternative Name:Cyanine 3-uridine-5’-triphosphate (enhanced)

Concentration:10mM

Formulation:Liquid. Solution in water.

Excitation maximum:550 nm

Emission maximum:564 nm

Extinction Coefficient:150,000 M-1 cm-1 (550 nm in TE [10 mM TRIS, pH 8.0, 1 mM EDTA])

Purity:≥93% (HPLC)

Purity Detail:Purified by ion-exchange chromatography.

Appearance:Dark pink liquid.

Shipping:Shipped on Dry Ice

Long Term Storage:-20°C

Use/Stability:Stable for at least one year after receipt when stored as recommended.

Handling:Protect from light. Avoid freeze/thaw cycles.

Technical Info/Product Notes:Several of Enzo’s products and product applications are covered by US and foreign patents and patents pending.

Regulatory Status:RUO - Research Use Only

<strong>Cyanine 3-UTP (enhanced)</strong> image
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<strong>Cyanine 3-UTP (enhanced)</strong> image


Product Literature References

Borna disease virus phosphoprotein triggers the organization of viral inclusion bodies by liquid-liquid phase separation: Y. Hirai, et al.; Int. J. Biol. Macromol. 192, 55 (2021), Abstract;
NORAD-induced Pumilio phase separation is required for genome stability: M.M. Elguindy, et al.; Nature (2021), Abstract;
Self-assembled Messenger RNA Nanoparticles (mRNA-NPs) for Efficient Gene Expression: H. Kim, et al. ; Sci. Rep. 5, 12737 (2015), Application(s): Labeling of mRNA-NPs, Abstract;


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