Nucleic Acid Synthesis
Biotium Biotin-16-UTP, 10 mM in pH 7.5 Tris-HCl Solution
Biotin-16-UTP can be enzymatically incorporated into RNA. The number “16” is the number of atoms in the linker between biotin and UTP. The length of the linker affects the incorporation efficiency of the biotin-UTP probe into RNA using RNA polymerases, and it also affects biotin/avidin or biotin/streptavidin. In general, the shorter the linker, the more efficiently the biotin-UTP is incorporated into RNA by RNA polymerases. On the other hand, the longer the linker, the better biotin can interact with avidin or streptavidin. Properties: Colorless liquid; Store at -20⁰C; C32H48N7O19P3SLi4; MW: 987.51.
![Research Products International Corp ATP [Adenosine-5'-triphosphate, disodium salt trihydrate], 25 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00006095-A30030-25.0.JPG-250.jpg)
Research Products International Corp ATP [Adenosine-5'-triphosphate, disodium salt trihydrate], 25 G
An essential nucleotide triphosphate with a variety of roles in energy metabolism, signal transduction and nucleic acid metabolism.
Apexbio Technology LLC 5-Br-UTP(Synonyms: 5-Bromo-UTP, 5-Br-uridine triphosphate, 5-Bromo-uridine 5'-triphosphate, 5-Br-U 5'-triphosphate), 50ul (100 mM).
5-Br-UTP is a chemically modified ribonucleoside triphosphate that incorporates a bromine substituent at the 5 position of uracil Upon enzymatic incorporation into RNA sequences this compound confers enhanced structural stability and tolerance to enzymatic degradation by nucleases Such modified ribonucleotides are frequently employed in SELEX (Systematic Evolution of Ligands by EXponential enrichment) methodologies to generate aptamers exhibiting improved resistance to nucleolytic cleavage and greater thermal robustness Consequently 5-Br-UTP holds relevance for RNA-based therapeutic research and aptamer engineering applications
LGC GENOMICS LLC 5'-Thiol Modifier C6 S-S CE-Phosphoramidite, Thiol-Reactive Group, Robust Conjugation Method, 10.74074074074074 g
The 5'-Thiol Modifier C6 S-S CE-Phosphoramidite is a versatile chemical reagent designed for the targeted incorporation of thiol groups into oligonucleotides, which allows for easy post-synthesis modifications. Its unique disulfide bridge and C6 spacer facilitate effective thiol liberation, enhancing conjugation efficiency for various applications including biosensing and microarrays. Unlike other modifiers, it simplifies purification processes, making it suitable for diverse bioconjugation needs.
Medchemexpress LLC 7-TFA-ap-7-Deaza-dG | 666847-77-4 | MFCD29904591 | 98.0% | C16H16F3N5O5 | 10MG
7-TFA-ap-7-Deaza-dG is a modified nucleoside (7-deaza-2'-deoxyguanosine) bearing a trifluoroacetylated propargyl linker. Supplied as a solid, it functions as a building block in oligonucleotide synthesis and as a reagent for click-chemistry labeling, enabling conjugation through its terminal alkyne for bioconjugation and probe attachment.
- 7-deaza 2'-deoxyguanosine core with trifluoroacetyl modification.
- Terminal alkyne (propargyl) handle for click chemistry conjugation.
- High purity suitable for research and synthesis.
- Solid form for convenient storage and handling.
- Compatible with nucleotide and oligonucleotide synthesis workflows.
Chem-Impex International, Inc. Adenine | 73-24-5 | MFCD00041790 | 25G
Adenine, 73-24-5, MFCD00041790, 25G
Chem-Impex International, Inc. 1-Methyl-2-pyrrolidinone, distilled | 872-50-4 | MFCD00003193 | 4L
1-Methyl-2-pyrrolidinone, distilled, 872-50-4, MFCD00003193, 4L
Revvity Health Sciences Inc HTRF High Performance Human IL-6 Detection Kit, 96 Assay Points
HTRF High Performance Human IL-6 Detection Kit, 96 Assay Points
Cayman Chemical N6 N6-DImethyladenosIn 500mg
A modified nucleoside; has been found in tRNA isolated from M. bovis; dimethylation of adjacent adenosine nucleosides is found in E. coli 16S rRNA and is important for the initiation of protein synthesis; inhibits the proliferation of L1210 leukemia cells in vitro (IC50 = 0.5 UG/ml) but does not have antitumor activity in vivo; a component of puromycin