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Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
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An optimized blend of a thermostable DNA Ligase and a proprietary additive, HiFi Taq DNA Ligase efficiently seals nicks in DNA with unmatched high fidelity. The formation of a phosphodiester bond between juxtaposed 5 phosphate and 3 hydroxyl termini of two adjacent oligonucleotides that are hybridized to a complementary target DNA is enhanced in the improved reaction buffer and mismatch ligation is dramatically reduced. The improved formulation allows higher resolution discrimination between ligation donors and acceptors, enabling precise detection of SNPs and other allele variants. HiFi Taq DNA Ligase is active at elevated temperatures (37-75C). Please note that HiFi Taq DNA Ligase is intended for use in molecular diagnostics applications that depend on high fidelity nick ligation. It is not a substitute for T4 DNA ligase and is not suitable for cloning applications or adapter ligation/NGS library prep.
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The ADAMTS-4/Aggrecanase FRET Substrate offers researchers a reliable tool for detecting ADAMTS-4 enzyme activity. With a quantity of 1 mg, this peptide substrate enables precise enzyme assays with FRET technology, distinguishing it from standard substrates. Its specific function in cartilage degradation pathways makes it vital for studies related to osteoarthritis and tissue remodeling. Easy to use and store, it supports ongoing research in enzyme substrates and inhibitors.
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Dabcyl–FRLKGGAPIKGV–Edans is an internally quenched fluorogenic substrate for the SARS-CoV or MERS-CoV family Papain-like protease (PLPro or PLP) that recognizes a LXGG consensus cleavage sites. Upon PLP-mediated cleavage between glycine and alanine, the resulting APIKGV-Edans fluorescence can be monitored at the excitation/emission wavelengths of 355/538 nm, respectively. In addition, PLP has deubiquitinating and deISG15ylation activities.
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Ac-ANW-AMC is a fluorogenic peptide substrate used to measure immunoproteasome β5i activity in vitro. Proteolytic cleavage releases 7-amino-4-methylcoumarin (AMC), producing a fluorescent signal suitable for kinetic or end-point assays.
releases AMC fluorophore upon proteolytic cleavage for fluorescence detection.
Caspase and granzyme substrate. Fluorogenic substrate for caspase-8/caspase-3 processing enzyme and granzyme B. Also a substrate for caspase-10. The IETD sequence is based on caspase-3 proenzyme cleavage site. Alternative Name: Caspase 8 substrate (fluorogenic), Granzyme B substrate (fluorogenic). Formula: C31H38F3N5O12. MW: 729.7. Purity: ≥98% (HPLC). Sequence Ac-Ile-Glu-Thr-Asp-AFC (AFC=7-Amino-4-trifluoromethylcoumarin). Appearance: White to off-white powder. Solubility: Soluble in DMSO. Long Term Storage: -20°C. Handling: Keep cool and dry.
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