Discover Tmr-shtl Accessory [URVB3OQd]

Discover Tmr-shtl Accessory [URVB3OQd]: Advanced Protein Tagging Solution

Discover Tmr-shtl Accessory [URVB3OQd], also known as CA-Sulfo-TMR or TMR-Sulfo-Halotag Ligand, is a state-of-the-art sulfonated HaloTag substrate designed for efficient protein tagging and purification. Engineered from the haloalkane dehalogenase DhaA, HaloTag is a powerful tool for the rapid and selective labeling of proteins. The inclusion of a sulfonate group on the amide bond linking the chloroalkane moiety to the TMR dye enhances the stability and fluorescence properties of the ligand. This unique feature makes Discover Tmr-shtl Accessory [URVB3OQd] an ideal choice for a wide range of research applications.

Key Product Features and Specifications

Discover Tmr-shtl Accessory [URVB3OQd] offers several key advantages that set it apart from other protein tagging solutions. With a purity of >= 95% by HPLC, it ensures high-quality results. Its molecular formula, C38H48ClN3O9S, and molecular weight of 758.32 make it a reliable and consistent choice for your research. The solubility of Discover Tmr-shtl Accessory [URVB3OQd] in DMSO and DMF allows for easy handling and use. Furthermore, the product is shipped on gel packs to maintain its integrity during transportation and storage, ensuring that you receive the highest quality product possible.

Practical Applications and Benefits

Discover Tmr-shtl Accessory [URVB3OQd] is a versatile tool with numerous practical applications. Its ability to form a stable covalent bond with chloroalkane substrates makes it an excellent choice for protein purification and isolation. The introduction of the charged sulfonate group minimally alters the excitation and emission profiles, ensuring consistent and reliable results. Additionally, Discover Tmr-shtl Accessory [URVB3OQd] demonstrates longer fluorescence lifetimes than its non-sulfonated counterparts, making it ideal for various imaging techniques. This powerful substrate is a valuable asset for researchers seeking to improve the efficiency and effectiveness of their protein tagging experiments.