2-déoxyuridine, 99 - 100 %

Code: d5412-1g D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

2′-Deoxyuridine has been used as a:precursor of [3H]thymidine triphosphate (TTP) in place of thymidine to avoid a potential thymidine block in relative proliferat...


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Votre prix
£115.00 1G

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

2′-Deoxyuridine has been used as a:precursor of [3H]thymidine triphosphate (TTP) in place of thymidine to avoid a potential thymidine block in relative proliferation assaysnucleoside supplement for cell cycle synchronization and DNA replication inhibitionmitotic inhibitor in culture media to minimize the proliferation of glial cells

Biochem/physiol Actions

2′-Deoxyuridine (dU) is frequently halogenated to create thymidine analogs useful for studies of DNA synthesis and degradation mechanisms. Derivatized 2′-deoxyuridines used as labeling substrates include chloro-2′-deoxyuridine (CldU), bromodeoxyuridine (BrdU) and/or iododeoxyuridine (IdU). Other useful analogs of 2′-deoxyuridine include 5-ethynyl-2′-deoxyuridine (DdU) and 5-hydroxymethyl-2′-deoxyuridine (HmdU).

Packaging

1, 5 g in poly bottle

100, 250 mg in poly bottle

assay≥98.5%
biological sourcesynthetic (organic)
formpowder
Gene Informationmouse ... Slc29a1(63959)
impuritiesThymidine, free
InChI keyMXHRCPNRJAMMIM-SHYZEUOFSA-N
InChI1S/C9H12N2O5/c12-4-6-5(13)3-8(16-6)11-2-1-7(14)10-9(11)15/h1-2,5-6,8,12-13H,3-4H2,(H,10,14,15)/t5-,6+,8+/m0/s1
Quality Level100
SMILES stringOC[C@H]1O[C@H](C[C@@H]1O)N2C=CC(=O)NC2=O
solubilitywater: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow
Code
Description
Unité de vente
Prix annoncé
Qté
D5412-100MG
Unité:100MG
Prix annoncé: £27.90
Source:Prix annoncé
D5412-250MG
Unité:250MG
Prix annoncé: £42.10
Source:Prix annoncé
D5412-5G
Unité:5G
Prix annoncé: £415.00
Source:Prix annoncé
Cas Number951-78-0
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