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Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
Prevent recircularization and religation of linearized cloning vector DNA by removing Phosphate groups from both 5'-termini, dephosphorylation of 5' Phosphorylated ends of DNA or RNA for subsequent labeling with (32P)ATP and T4 Polynucleotide Kinase
The AttoPhos(R) Buffer is optimized for sensitive detection of alkaline phosphatase (AP) when used to prepare working solutions with AttoPhos(R) Substrate.
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Capable of digesting DNA in 15 minutes or less. Available at high concentration, containing 5,000 units of RsaI at a concentration of 40-80u/μL. (GT/AC CA\TG)
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Capable of digesting DNA in 15 minutes or less. Blue/white cloning qualified, providing a higher level of quality control for enzymes used in cloning applications. (G/GATC C C CTAG\G)
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Glu-C, Sequencing Grade (S. aureus V8), is a serine protease that specifically cleaves at the C-terminus of either aspartic or glutamic acid residues. Glu-C activity is optimal in the pH range of 4.0-9.0 and suitable for digestion reactions in solution.
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Pepsin preferentially cleaves at the C-terminus of phenylalanine, leucine, tyrosine and tryptophan. Pepsin can be used alone or with other proteases for protein analysis by mass spectrometry and other applications. Activity is optimal at pH 1.0-3.0.
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