5(6)-TAMRA PEG3 azide acid Unlike traditional chemical reactions utilizing

Unlike traditional chemical reactions utilizing succinimidyl esters or maleimides that target amines and sulfhydryls – functional groups that are not unique – click chemistry-labeled molecules can be applied to complex biological samples and be detected with unprecedented sensitivity due to extremely low background

382 SMILES OCCCCCNC1=C2C(=O)N(C3CCC(=O)NC3=O)C(=O)C2=CC=C1 Purity (HPLC) >= 95% Shipping Conditions Room temperature Storage Conditions Refrigerated Shelf Life 12 months after the date of delivery Regulatory Statement For Research Use Only

401 SMILES OC(=O)CCOCCOCCOC1=C2C(=O)N(C3CCC(=O)NC3=O)C(=O)C2=CC=C1 Purity (HPLC) >= 95% Shipping Conditions Room temperature Storage Conditions Refrigerated Shelf Life 12 months after the date of delivery Regulatory Statement For Research Use Only

The two-step reaction procedure involves a copper-catalyzed triazole formation of an azide and an alkyne

5(6)-TAMRA PEG3 azide acid Unlike traditional chemical reactions utilizingThe water soluble 5(6) TAMRA PEG3 azide has a long PEG3 spacer that separates the dye tetramethylrhodamine (commonly known as TMR or TAMRA) from the terminal azide group. The water soluble PEG3 spacer should minimize the interaction between the dye and the biomolecule to be labeled. With excitation maximum at 547 nm, the acetylene TMR conjugate is an excellent match to the intense 546 nm spectral line of the mercury arc laps used in most fuorescence