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2′-Deoxyadenosine 5′-monophosphate disodium
2′-Deoxyadenosine 5′-monophosphate disodium
CAS No. 2922-74-9
2′-Deoxyadenosine 5′-monophosphate disodium ( —— )
Catalog No. M28292 CAS No. 2922-74-9
2′-Deoxyadenosine 5′-monophosphate disodium, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate disodium can be used to study adenosine-based interactions during DNA synthesis and DNA damage.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product Name2′-Deoxyadenosine 5′-monophosphate disodium
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NoteResearch use only, not for human use.
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Brief Description2′-Deoxyadenosine 5′-monophosphate disodium, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate disodium can be used to study adenosine-based interactions during DNA synthesis and DNA damage.
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Description2′-Deoxyadenosine 5′-monophosphate disodium, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate disodium can be used to study adenosine-based interactions during DNA synthesis and DNA damage.(In Vitro):2′-Deoxyadenosine 5′-monophosphate (dAMP) is incorporated into Caco-2 cells in a time-dependent manner. The uptake of 2′-Deoxyadenosine 5′-monophosphate is increased with a drop in pH, suggesting that 2′-Deoxyadenosine 5′-monophosphate transport activity might be linked to the protons. 2′-Deoxyadenosine 5′-monophosphate uptake by Caco-2 cells is pH- and Na+-dependent.
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Synonyms——
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PathwayProteasome/Ubiquitin
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TargetEndogenous Metabolite
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RecptorROS;P450;Trypsin
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Research Area——
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Indication——
Chemical Information
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CAS Number2922-74-9
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Formula Weight375.2
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Molecular FormulaC10H12N5Na2O6P
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Purity>98% (HPLC)
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Solubility——
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SMILES[Na+].[Na+].Nc1ncnc2n(cnc12)C1CC(O)C(COP([O-])([O-])=O)O1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Biskup E, et al. Triterpenoid α-amyrin stimulates proliferation of human keratinocytes but does not protect them against UVB damage. Acta Biochim Pol. 2012;59(2):255-60. Epub 2012 May 11.
molnova catalog
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