Description

Our dNTPs are analytically tested to ensure a purity of >99% by HPLC, guaranteeing optimal performance in demanding PCR applications.

Specification

Parameter	Specification
Purity	≥ 99% (HPLC)
Total Product Size	0.5 mL
Individual Container Size	0.5 mL
Number of Containers	1
Refrigeration Requirements	Freezer
Shipping Conditions	ICE
UNSPSC Code	12352208
UNSPSC Category	Nucleic Acid Bases
Grade	Biotech
DG	No
Storage	(-15 to -20)℃
Sterile	No
Stock	Usually in Stock

Summary

DNase, RNase: None detected.

Suitable for use in the Polymerase Chain Reaction (PCR).

PCR Suitability

dNTP Mix is a solution containing each of the four deoxynucleotides as follows:

25 mM dATP
25 mM dCTP
25 mM dGTP
25 mM dTTP

dNTP Mix was tested at a final concentration of 200 μM in a reaction mixture containing10 mM Tris-HCl, pH 8.3 at 25 °C, 50 mM KCl, 1.5 mM MgCl2, 0.001% (w/v) gelatin, primers defining an approximately 500 base pair region of λ DNA at 1.0 μM each, λ DNA template at 1 ng/100 μl, and Taq DNA polymerase at 2.5 units/100 μl. The reaction underwent 25 cycles of 94 °C to denature the double stranded DNA, 55 °C to anneal the DNA segments, and 72 °C to extend the DNA segments. A single band of approximately 500 base pairs was visualized following electrophoresis of the reaction product in a 1.5% agarose gel.

Quality Control

Endonuclease-Exonuclease
One μg of λ Hind III fragments was incubated for 16 hours at 37 °C with dNTP Mix at a final concentration of 5 mM in a 50 μl reaction mixture containing 30 mM TrisHCl, pH 7.8, 50 mM NaCl and 10 mM MgCl2. No degradation of the DNA fragments was detected following agarose gel electrophoresis. Detection limit: Degradation of 10% of the DNA substrate is detectable.

Endonuclease (Nickase)
One μg of pBR322 DNA was incubated for 16 hours at 37 °C with dNTP Mix at a final concentration of 5 mM in a 50 μl reaction mixture containing 30 mM Tris-HCl, pH 7.8, 50 mM NaCl and 10 mM MgCl2. No conversion of the covalently closed circular DNA to the nicked or linear form was observed following agarose gel electrophoresis. Detection limit: Conversion of 1% of the DNA substrate is detectable.

RNase
Two μg of transfer RNA were incubated for 16 hours at 37 °C with dNTP Mix at a final concentration of 5 mM in a 50 μl reaction mixture containing 30 mM Tris-HCl, pH 7.8, 50 mM NaCl and 10 mM MgCl2. No degradation of the tRNA was detected following polyacrylamide gel electrophoresis. Detection limit: Degradation of 10% of the tRNA substrate is detectable.

Documents

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Disclaimer

For laboratory research use only.

dNTP mixture (25mM)