Biotin alkyne
Cat. # | Quantity | Price | Lead time | Buy this product |
---|---|---|---|---|
C37B0 | 10 mg | $135 | in stock | |
D37B0 | 25 mg | $325 | in stock | |
E37B0 | 50 mg | $575 | in stock | |
F37B0 | 100 mg | $1150 | in stock |
Biotin alkyne for the preparation of various biotinylated conjugates via click reaction.
This alkyne reacts with various azides, including biomolecules containing azide groups. Biotinylated conjugates can be used for various assays and applications requiring affinity binding.
Our recommended protocol can be used for the conjugation.
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Appearance: | colorless solid |
Molecular weight: | 281.37 |
CAS number: | 773888-45-2 |
Molecular formula: | C13H19N3O2S |
Solubility: | good in DMSO and DMF, low in water |
Quality control: | NMR 1H (95%), TLC, functional testing |
Storage conditions: | Storage: 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. |
MSDS: | Download |
Product specifications |
Product citations
- Bin Rashed, F.; Stoica, A.C.; MacDonald, D.; El-Saidi, H.; Ricardo, C.; Bhatt, B.; Moore, J.; Diaz-Dussan, D.; Ramamonjisoa, N.; Mowery, Y.; Damaraju, S.; Fahlman, R.; Kumar, P.; Weinfeld, M. Identification of proteins and cellular pathways targeted by 2-nitroimidazole hypoxic cytotoxins. Redox Biology, 2021, 41, 101905. doi: 10.1016/j.redox.2021.101905
- Clavé, G.; Vasseur, J.-J.; Smietana, M. The Sulfo-Click Reaction and Dual Labeling of Nucleosides. Current Protocols in Nucleic Acid Chemistry, 2020, 83(1), e120. doi: 10.1002/cpnc.120
- Rink, W.M.; Thomas, F. Decoration of Coiled-Coil Peptides with N-Cysteine Peptide Thioesters As Cyclic Peptide Precursors Using Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) Click Reaction. Organic Letters, 2018, 20(23), 7493–7497. doi: 10.1021/acs.orglett.8b03261
- Cui, X.-Y.; Sun, N.-N.; Xie, X.-N.; Sun, W.-C.; Zhao, Q.; Liu, N. Detection of Newly Synthesized Proteins via Metabolic Incorporation of Non-natural Amino Acid. Chinese Journal of Analytical Chemistry, 2018, 46(11), 1808–1813. doi: 10.1016/s1872-2040(18)61125-9
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