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4-Thio-UTP

s4UTP, 4sUTP

4-Thio-uridine-5'-triphosphate, Sodium salt

Cat. No. Amount Price (EUR) Buy / Note
NU-1156S 10 μl (100 mM)103,10 Add to Basket/Quote Add to Notepad
NU-1156L 5 x 10 μl (100 mM)352,16 Add to Basket/Quote Add to Notepad
Structural formula of 4-Thio-UTP (s4UTP, 4sUTP, 4-Thio-uridine-5'-triphosphate, Sodium salt)
Structural formula of 4-Thio-UTP

For general laboratory use.

Shipping: shipped on gel packs

Storage Conditions: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.

Shelf Life: 12 months after date of delivery

Molecular Formula: C9H15N2O14P3S (free acid)

Molecular Weight: 500.20 g/mol (free acid)

Exact Mass: 499.95 g/mol (free acid)

Purity: ≥ 95 % (HPLC)

Form: solution in water

Color: colorless to slightly yellow

Concentration: 100 mM - 110 mM

pH: 7.5 ±0.5

Spectroscopic Properties: λmax 331 nm, ε 16.3 L mmol-1 cm-1 (Tris-HCl pH 7.5)

Applications:
Potent agonist for P2Y2 and P2Y4 receptors[1,4]
Labeling of transcriptional complex[2]
Influence on elongation and termination events and evoking transcriptional pause[3]

Related products:

BIOZ Product Citations:

Selected References:
[1] Jacobson et al. (2006) Structure activity and molecular modeling analyses of ribose- and base-modified uridine 5-triphosphate analogues at the human P2Y2 and P2Y4 receptors. Biochemical Pharmacology 71 (4):540.
[2] Khanna et al. (1991) Photoaffinity labelling of the pea chloroplast transcriptional complex by nascent RNA in vitro. Nucleic Acids Res. 19 (18):4849.
[3] Dissinger et al. (1990) Active site labeling of Escherichia coli transcription elongation complexes with 5-[(4-azidophenacyl)thio]uridine 5'-triphosphate. J. Biol. Chem. 265 (13):7662.
[4] Shaver et al. (1997) 4-substituted uridine 5'-triphosphates as agonists of the P2Y2 purinergic receptor. Nucleosides and Nucleotides 16 (7):1099.
[5] Munchel et al. (2011) Dynamic profiling of mRNA turnover reveals gene-specific and system-wide regulation of mRNA decay. Mol. Biol. Cell 22 (15):2787.
[6] Zaher et al. (2006) A general RNA-capping ribozyme retains stereochemistry during cap exchange. J. Am. Chem. Soc. 128 (42):13894.
[7] Kwon et al. (2001) DNA sequencing and genotyping by transcriptional synthesis of chain-terminated RNA ladders and MALDI-TOF mass spectrometry. Nucleic Acids Res. 29 (3):e11.
[8] Testa et al. (1999) Thermodynamics of RNA-RNA Duplexes with 2- or 4-Thiouridines: Implications for Antisense Design and Targeting a Group I Intron. Biochemistry 38:16655.
[9] Dontsova et al. (1994) Stem-loop IV of 5S rRNA lies close to the peptidyltransferase center. Proc. Natl. Acad. Sci. USA 91 (10):4125.
[10] Sheng et al. (1993) Active site labeling of HIV-1 reverse transcriptase. Biochemistry 32 (18):4938.
[11] Khanna et al. (1991) Photoaffinity labelling of the pea chloroplast transcriptional complex by nascent RNA in vitro. Nucleic Acids Res. 19 (18):4849.
[12] Tanner et al. (1988) Binding interactions between yeast tRNA ligase and a precursor transfer ribonucleic acid containing two photoreactive uridine analogues. Biochemistry 27 (24):8852.
[13] Bartholomew et al. (1986) RNA contacts subunits IIo and IIc in HeLa RNA polymerase II transcription complexes. J. Biol. Chem. 261 (30):14226.
[14] Eshaghpour et al. (1979) Specific chemical labeling of DNA fragments. Nucleic Acids Res. 7 (6):1485.