The rTrypsin 3.0 and rLys C enzyme mix combines two recombinant proteases for efficient peptide bond hydrolysis. rTrypsin 3.0 cleaves at the carboxyl side of lysine and arginine residues, while rLys C targets lysine residues specifically. This combination minimizes missed cleavages caused by rTrypsin’s slower digestion of lysine and arginine, PTMs on lysines, or hydrophobic C-termini (e.g., proline). The rTrypsin and rLys C mix is ideal for protein characterization, single-cell proteomics, and large cohort proteomics studies.
Physical Appearance
Lyophilized powder with 67 µg Trehalose
Molecular Weight
rTrypsin 23.7 kDa; rLys C 27 kDa
Resuspension Buffer
Dissolve in 40 µL of 50 mM acetic acid to a concentration of 0.5 µg/µL
rTrypsin 3.0/rLys C is maximally active in the pH range of 7–9
Usage Notes
1. Suitable digestion buffers: 20 mM Tris, 50 mM ABC, or HEPES buffer (pH 7–9). 2. Use denatured protein samples at a 1:50 protease-to-protein ratio. Maintain a protein concentration of 0.5 µg/µL and incubate at 37°C for 30 minutes.