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  2. Fluorescent Dye DNA Stain
  3. Cy3-dCTP

Cy3-dCTP is a directly fluorescently labeled deoxyribonucleotide, in which Cy3 is a cyanine fluorescent dye. Cy3-dCTP is used for direct enzymatic labeling of DNA and cDNA: with the aid of DNA polymerases, this modified nucleotide is incorporated into the extending DNA strand during processes such as reverse transcription, PCR, nick translation or random primer labeling.

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Cy3-dCTP

Cy3-dCTP Chemische Struktur

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Solvent
1 mg (10 mM * 86.43 μL in Water) Auf Lager
Solvent
5 mg (10 mM * 432.15 μL in Water) Auf Lager

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Beschreibung

Cy3-dCTP is a directly fluorescently labeled deoxyribonucleotide, in which Cy3 is a cyanine fluorescent dye. Cy3-dCTP is used for direct enzymatic labeling of DNA and cDNA: with the aid of DNA polymerases, this modified nucleotide is incorporated into the extending DNA strand during processes such as reverse transcription, PCR, nick translation or random primer labeling[1][2].

In Vitro

Guide (The following is our recommended protocol. This protocol is only a guide and should be modified according to your specific needs).
While specific steps vary by application, a standard direct labeling protocol (e.g., for microarrays or FISH) generally follows these stages:
1. Reaction Setup
1.1 Mix the DNA or RNA template with primers (e.g., oligo dT or random hexamers).
1.2 Prepare a dNTP mix where a portion of the natural dCTP is replaced by Cy3-dCTP.
1.3 Recommended Ratio: A common ratio is 30–50% Cy3-dCTP to 50–70% unlabeled dCTP to balance labeling efficiency with enzyme processivity.
2. Enzymatic Incorporation
2.2 Add the appropriate enzyme (e.g., Klenow fragment for DNA, Reverse Transcriptase for RNA, or Taq polymerase for PCR).
2.3 Incubate at the enzyme's optimal temperature (e.g., 37°C for Klenow/RT or cycling for PCR).
3. Stopping and Purification:
3.1 Stop the reaction using EDTA (HY-Y0682) or heat inactivation.
3.2 Crucial Step: Remove unincorporated nucleotides using a spin column, ethanol precipitation, or centrifugal filters. This is essential to minimize background fluorescence during downstream applications.
4. Analysis:
4.1 Measure the concentration and labeling efficiency (dye incorporation) using a spectrophotometer like a NanoDrop.
4.2 Read absorbance at 260 nm (DNA) and 550 nm (Cy3).

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molekulargewicht

1156.71

Formel

C43H51Li4N6O20P3S2

Appearance

Liquid

Color

Pink to red

SMILES

O=S(C1=CC2=C(C=C1)C(C)(C)C(/C=C/C=C3N(CCCCCC(NCC#CC4=CN(C5OC(COP(OP(OP(O[Li])(O[Li])=O)(O[Li])=O)(O[Li])=O)C(O)C5)C(N=C4N)=O)=O)C6=C(C=CC(S(=O)(O)=O)=C6)C/3(C)C)=[N+]2CC)([O-])=O

Versand

Room temperature in continental US; may vary elsewhere.

Speicherung

Solution, -20°C, protect from light, 2 years

Reinheit & Dokumentation

Purity: 98.70%

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  • Molaritätsrechner

  • Verdünnungsrechner

Die Formel zur Berechnung von Molaritäten

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
= × ×

The dilution calculator equation

Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)

Diese Gleichung wird häufig abgekürzt als: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Cy3-dCTP
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