Description
Boc-Gly-Arg-Arg-AMC acetate salt is a protected fluorogenic peptide substrate supplied at a minimum purity of 98 % for enzymatic and biochemical assays. It carries CAS number 113866-14-1 and the empirical formula C₂₉H₄₄N₁₀O₇(C₂H₄O₂)ₓ, reflecting the Boc-masked Gly-Arg-Arg sequence linked to the 7-amino-4-methylcoumarin (AMC) reporter as an acetate salt. Cleavage after the arginine residues releases free AMC, enabling sensitive fluorescence readout in protease activity measurements, inhibitor screening and kinetic studies. The Boc group facilitates controlled handling in peptide-related workflows, while the dibasic recognition motif is suited to trypsin-like and related serine protease investigations. This specialty biochemical from manufacturer Carl ROTH gives laboratories a characterised AMC substrate for method set-up and comparative enzyme work based on the stated identity and purity.
This article is part of Click chemistry, bioconjugation & synthesis reagents, in Biochemicals & reagents.
Key features
- CAS number: 113866-14-1
- Pack sizes: 1 mg, 2 mg, 5 mg, 10 mg, 25 mg
- Purity: min. 98 %
- Empirical formula: C₂₉H₄₄N₁₀O₇(C₂H₄O₂)ₓ
- Storage temperature: -20 °C
- Salt form: acetate salt
- Technical Information Sheet:
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Questions about Boc-Gly-Arg-Arg-AMC acetate salt, min. 98 %, 1 mg
What is this article?
Boc-Gly-Arg-Arg-AMC acetate salt, min. 98 %, 1 mg is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Click chemistry, bioconjugation & synthesis reagents, inside Biochemicals & reagents, in Microbiology lab supplies.
Click and bioconjugation reagents join two molecules under mild conditions, often an azide to an alkyne, or an NHS ester to an amine. The linker length and the reactive group are the specification. They are small bottles of a reactive compound, and moisture often ruins them.
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