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dNTP Mix dUTP / 10 mM

Premix of 10 mM dATP, dCTP, dGTP and 20 mM dUTP

2'-Deoxyadenosine 5'-triphosphate, Sodium salt; 2'-Deoxycytidine 5'-triphosphate, Sodium salt; 2'-Deoxyguanosine 5'-triphosphate, Sodium salt; 2'-Deoxyuridine 5'-triphosphate, Sodium salt

Cat. No. Amount Price (EUR) Buy / Note
NU-1020S 200 μl 23,24 Add to Basket/Quote Add to Notepad
NU-1020L 1 ml 92,96 Add to Basket/Quote Add to Notepad
Structural formula of dNTP Mix dUTP / 10 mM (Premix of 10 mM dATP, dCTP, dGTP and 20 mM dUTP, 2'-Deoxyadenosine 5'-triphosphate, Sodium salt; 2'-Deoxycytidine 5'-triphosphate, Sodium salt; 2'-Deoxyguanosine 5'-triphosphate, Sodium salt; 2'-Deoxyuridine 5'-triphosphate, Sodium salt)
Structural formula of dNTP Mix dUTP / 10 mM

For in vitro use only!

Shipping: shipped on blue ice

Storage Conditions: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible. If stored as recommended, Jena Bioscience guarantees optimal performance of this product for 12 months after date of delivery.

Shelf Life: 12 months

Molecular Formula: C10H13N5O12P3 (Anion); C9H13N3O13P3 (Anion); C10H13N5O13P3 (Anion); C9H12N2O14P3 (Anion)

Molecular Weight: 488.16 g/mol (Anion); 464.13 g/mol (Anion); 504.16 g/mol (Anion); 465.12 g/mol (Anion)

Purity: ≥ 99 % (HPLC)

Form: clear aqueous solution

pH: 8.5 ±0.2 (22 °C)

Description:
dNTP Mix incl. dUTP is an mixture of 10 mM ultrapure dATP, dCTP, and dGTP, and 20 mM dUTP supplied as clear aqueous solution (pH 8.5). dUTP can be used in place of dTTP in PCR and RT-PCR protocols to prevent carry-over contaminations from previous amplifications.

Quality Control Specifications:
Low Copy Long Range PCR (4 kb, lambda DNA, template dilution series): PCR fragment with 10 pg of template or less
Contamination with bacterial or human DNA: not detectable
DNases, RNases, Nicking Activity: not detectable
Proteases: not detectable

Selected References:
Erlich et al. (1988) Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 29 (239):487.
Holland et al. (1991) Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase. Proc. Natl. Acad. Sci. USA 88 (16):7276.
Sanger et al. (1977) DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74:5463.