Purine nucleosides
Cambridge Isotope Laboratories 2-Fluoro-2-deoxyguanosine 5-triphosphate ammonium salt (unlabeled) (in solution) CP 90% 100 umol
2-Fluoro-2-deoxyguanosine 5-triphosphate ammonium salt (unlabeled) (in solution) CP 90% 100 umol
Cambridge Isotope Laboratories 2-Deoxyadenosine monohydrate (13C10 98% 15N5 96-98%) 10 mg
2-Deoxyadenosine monohydrate (13C10 98% 15N5 96-98%) 10 mg
Sigma Aldrich Fine Chemicals Biosciences 2'-Deoxyguanosine monohydrate 99-100% | 312693-72-4 | MFCD00150760 | 5G
2'-Deoxyguanosine monohydrate 99-100% | Purity: 99-100% | Mol Wt: 285.26 | 312693-72-4 | MFCD00150760 | 5G
Medchemexpress LLC 2'-deoxyguanosine | 961-07-9 | MFCD00080300 | 99.2% | 267.24 g/mol | C10H13N5O4 | 10 MG
2'-Deoxyguanosine (standard) is the analytical standard of 2'-deoxyguanosine, a purine nucleoside used as an analytical reference and research reagent. Supplied as a high-purity solid, it is intended for analytical assays, method development, and quantitative reference applications.
- Analytical standard suitable for quantitative assays and calibration.
- High purity (99.2%) for reliable analytical results.
- Molecular weight 267.24 g/mol; formula C10H13N5O4 for accurate identification.
- Available in small pack sizes for method development and trace analyses.
- Supplied with certificate of analysis and recommended storage guidance.
Chem-Impex International, Inc. N2-Isobutyryl-2'-deoxyguanosine | 68892-42-2 | MFCD00010060 | 25G
N2-Isobutyryl-2'-deoxyguanosine, 68892-42-2, MFCD00010060, 25G
Biotium MUC1 / CA15-3 / EMA / CD227 (Epithelial Marker)(VU-4H5), CF740 conjugate, 0.1mg/mL
MAb VU-4H5 reacts with MUC1, a large transmembrane glycoprotein expressed on the ductal surface of normal glandular epithelia. The dominant epitope of MAb VU4H5 is APDTR as established with 'epitope fingerprinting'. VU-4H5 preferentially binds to under-glycosylated 'tumor' MUC1. The extracellular domain of MUC1 largely consists of a highly conserved, O-glycosylated 20 amino acids tandem repeat which can occur 30-100 times per molecule depending on the length of the allele involved. In the vast majority of human carcinomas this protein is upregulated and poorly glycosylated and appears on the cell surface in a non-polarized fashion. Antibody to EMA is useful as a pan-epithelial marker for detecting early metastatic loci of carcinoma in bone marrow or liver.
Medchemexpress LLC 2-Deoxyadenosine 5 250mg
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[1]
eMolecules 312693-72-4 | 2'-Deoxyguanosine monohydrate | 1g
Ambeed | 1-(2-Methoxyphenyl)-1H-imidazole-5-carboxylic acid | 100mg | 600849156 | A866307 | 762240-23-3 | MFCD25368751 | 218.212 | C11H10N2O3
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Medchemexpress LLC 2'-Deoxyguanosine-13C10,15N5 monohydrate | 2483830-26-6 | 99.8% | 1 MG
2'-Deoxyguanosine-13C10,15N5 (monohydrate) is the 13C and 15N labeled 2'-Deoxyguanosine monohydrate, which is an endogenous metabolite. It is for research use only and not sold to patients.
- Used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules for quantitation during the drug development process.
- Deuteration has potential to affect pharmacokinetic and metabolic profiles of drugs.
Sigma Aldrich Fine Chemicals Biosciences 2 Deoxyadenosine monohydra25G
2 Deoxyadenosine monohydra25G
Medchemexpress LLC 2'-Deoxyguanosine 5'-monophosphate disodium hydrate | 146877-98-7 | 99.0% | C10H14N5O7.H2O.2Na | 100 MG
2'-Deoxyguanosine 5'-monophosphate disodium hydrate (dGMP) is an oxidizable target of the photosensitizer pterin. It can be used to evaluate the photosensitizing properties of biopterins. Pterin causes a photosensitive reaction of dGMP under UV-A radiation, leading to DNA damage. This process involves two main mechanisms in vitro for the photosensitive oxidation of purine nucleotides by pterin.
- A hydrogen abstraction reaction of electron transfer from dGMP to the triplet excited state of pterin (type I mechanism).
- Interaction between dGMP and pterin produces singlet molecular oxygen (1O2) (type II mechanism).