dGTP - Solution
For research use only.
Please centrifuge briefly before opening (volume ≤2 ml).
Description:
dGTP, PCR-grade is supplied as ultrapure aqueous solution (pH 8.5) and suitable for all molecular biology applications including PCR/qPCR, reverse transcription, DNA labeling and DNA sequencing.
Shipping: shipped on gel packs
Storage Conditions: store at -20 °C
Shelf Life: 12 months
Molecular Formula: C10H16N5O13P3 (free acid)
Molecular Weight: 507.18 g/mol (free acid)
CAS#: 93919-41-6
Purity: ≥ 99 % (HPLC)
Form: clear aqueous solution
Concentration: 100 mM - 110 mM
pH: 8.5 ±0.2 (22 °C)
Spectroscopic Properties: λmax 252 nm, ε 14.2 L mmol-1 cm-1 (Tris-HCl pH 7.0)
Selected References:
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.
Erlich et al. (1988) Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 29 (239):487.
Sanger et al. (1977) DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74:5463.
| Cat. No. | Amount | Price |
|---|---|---|
| NU-1003L | 1 ml (100 mM) | 96,60 € |
| NU-1003-10ML | 10 ml (100 mM) | 675,90 € |
| NU-1003-100ML | 100 ml (100 mM) | Ask for Quotation |
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Scientific citations for Jena Bioscience nu-1003
21 scientific citations and 4 citation images found by Bioz.
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Promoter strength and position govern promoter competition through transcript-dependent insulation.
Nature genetics, 2026-08-07 · PMID:42477113
Abstract: Long-range competition among promoters within a shared regulatory landscape has been implicated in development and disease, but the determinants of promoter competition remain unclear. Here we introduce diverse promoters into defined genomic sites within the Sox2 locus and measure how these insertions attenuate endogenous Sox2 expression. We find that the level of reduction in endogenous Sox2 transcription is correlated with the strength of the inserted promoter
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Socially regulated genes are spatially hyperconnected to enhancers in the ant brain
bioRxiv, 2026-04-09 · DOI:10.64898/2026.04.08.717219
PrePrint: 25 μL of “End-Labelling Mix” containing 1x T4 DNA ligase buffer (Enzymatics, L6030-HC-L), 0.2 mM biotin-14-dATP (Jena Bioscience, NU-835-BIO14-S), 0.2 mM biotin-14-dCTP (Jena Bioscience, NU-809-BIOX-S), 0.2 mM dTTP (Jena Bioscience, NU-1004L), 0.2 mM dGTP (
Jena Bioscience , ), and 0.1% BSA was then added to the sample for an incubation of 45 min at 25°C on a shaking Thermomixer.NU-1003 L -
Structural basis for CTCF-mediated chromatin organization
bioRxiv, 2026-02-08 · DOI:10.64898/2026.02.06.704447
PrePrint: .. 0.5 U/μL, and incubation was continued for an additional 15 minutes at 37 °C.. End repair was followed by a fill-in reaction using biotin-dATP and biotin-dCTP (Jena Bioscience, cat. no. NU-835-BIO14 and NU-809-BIOX) together with dGTP and dTTP (
Jena Bioscience , cat. no.NU1003 and NU1004), each at 66 μM, for 45 minutes at 25 °C.. Reactions were terminated by adding EDTA to a final concentration of 30 mM and ..
