Product protein-crosslinkers-bioconjugation-products

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Catalog	name	Description	price
R-M2-10919	Biotin-Methylthioadenosine	Biotin-Methylthioadenosine/Methylthioadenosine-Biotin‌(standard full name 5-Deoxy-5- Methylthioadenosine-Biotin) is an affinity labeled nucleoside derivative obtained by directed covalent coupling of natural metabolite 5- methylthioadenosine (MTA) with biotin. It is currently a core research tool molecule in the field of nucleoside interacting protein screening.	price>
R-M2-10925	Biotin-Salvianolic acid A	Biotin-Salvianolic acid A /Biotin labeled Salvianolic acid A is an affinity type scientific probe obtained by directed covalent coupling of natural active ingredient Salvianolic acid A with biotin. It retains the biological activity of Salvianolic acid A completely and adds the ultra-high specific binding ability of biotin streptavidin. It is a core tool molecule in the field of natural product target screening.	price>
R-M2-10926	Biotin-Palmitoleic acid	Biotin labeled Palmitoleic acid is an affinity type lipid probe obtained by directed covalent coupling, which fully retains the biological activity of palmitoleic acid and adds the ultra-high specificity binding ability of biotin streptavidin. It is a core research tool molecule in the fields of lipid metabolism and target screening.	price>
R-M2-10933	Biotin-Retinoic acid	Biotin-Retinoic acid/Biotin labeled retinoic acid is an affinity based research probe obtained by directed covalent coupling of all trans retinoic acid and biotin, which fully preserves the biological activity of retinoic acid and adds the ultra-high specificity binding ability of biotin streptavidin. It is a core tool molecule in the field of retinoic acid target screening and interacting protein identification.	price>
R-M2-10939	Biotin-Pemetrexed disodium	Biotin-Pemetrexed disodium/Biotin labeled Pemetrexed disodium is a research grade affinity tracer probe used only in laboratory studies and cannot replace clinical chemotherapy drugs. Through the streptavidin pull-down experiment, the direct binding target of pemetrexed was accurately enriched and identified from the whole protein lysate of tumor cells, and the deep molecular mechanism of overcoming tumor drug resistance was analyzed. As an affinity probe, quantitatively verify the specific binding efficiency between pemetrexed modified nanoparticles and folate receptors, and accurately quantify the active targeting performance of targeted drug delivery systems.	price>

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