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Peptides shop · Rhodamine 110, bis-(L-aspartic acid amide) · Reference sheet

Rhodamine 110, bis-(L-aspartic acid amide)

Reference sheet · Enzyme Substrates · CPC catalog code CASP-065

Identity

Name
Rhodamine 110, bis-(L-aspartic acid amide)
Catalog code
CASP-065
Category
Enzyme Substrates

Physicochemical properties

Sequence
(H-Asp)2-R110

Handling, storage & reconstitution

Upstream storage
CONDITIONS:**-20 ± 5 °C

General guidance for this class

Reference standards in the Enzyme Substrates class are typically shipped as lyophilized powder and stored desiccated at −20 °C protected from light. Once reconstituted in bacteriostatic water or the assay-appropriate buffer, aliquot and store at −80 °C to minimize freeze–thaw cycles. Confirm handling requirements against your institutional biosafety and radiation protocols before use.

Mechanism & research applications

Rhodamine 110, bis-(L-aspartic acid amide) sits within the Enzyme Substrates research class (CPC reference CASP-065). The peptide encodes a recognition sequence flanked by a reporter group (pNA, AMC, MCA, FAM/DABCYL). Enzyme cleavage releases the reporter, producing a quantifiable optical signal proportional to catalytic activity. Investigators typically incorporate Rhodamine 110, bis-(L-aspartic acid amide) as a reference standard, tool ligand, or substrate in the assay contexts listed above. Read on kinetic plate readers with the reporter-appropriate filter set (e.g. 405 nm, 380/460 nm).

Studied for

  • Kinetic (kcat / Km) characterization of proteases and hydrolases
  • High-throughput inhibitor screening
  • Selectivity profiling across related enzyme families
  • Diagnostic and academic activity assays

Frequently asked

What is Rhodamine 110, bis-(L-aspartic acid amide)?

Rhodamine 110, bis-(L-aspartic acid amide) (CPC catalog code CASP-065) is a synthetic enzyme substrate (research reagent) in the enzyme substrates category. It is provided as a lyophilized ~1 mg vial for in-vitro research use only.

What is Rhodamine 110, bis-(L-aspartic acid amide) studied for?

Published and internal research programs use Rhodamine 110, bis-(L-aspartic acid amide) as a reference standard in enzyme substrates workflows — for example, kinetic (kcat / km) characterization of proteases and hydrolases and high-throughput inhibitor screening. Human clinical evidence is not established.

Is Rhodamine 110, bis-(L-aspartic acid amide) FDA-approved for human use?

No. Rhodamine 110, bis-(L-aspartic acid amide) is a research-grade reference peptide and is not approved by the FDA or any national regulator for human or veterinary therapeutic use. It is offered exclusively for in-vitro laboratory research and does not ship to the United States for consumer use.

How is Rhodamine 110, bis-(L-aspartic acid amide) typically used in the lab?

In a enzyme substrates workflow, Rhodamine 110, bis-(L-aspartic acid amide) is reconstituted in sterile buffer or DMSO (solubility-dependent) and applied in the researcher's chosen assay format. Read on kinetic plate readers with the reporter-appropriate filter set (e.g. 405 nm, 380/460 nm).

Sources

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Related peptides in Enzyme Substrates

Other reference standards in the same class — commonly cross-referenced during assay design and comparator selection.

Rhodamine 110, bis-(CBZ-L-phenylalanyl-L-arginine amide)
Rhodamine 110, bis-(p-tosyl-L-glycyl-L-prolyl-L- arginine amide)
Rhodamine 110, bis-(CBZ-L-arginine amide), dihydrochloride (BZAR)
Rhodamine 110, bis-(CBZ-L-alanyl-L-arginine amide), dihydrochloride
Rhodamine 110, bis-(CBZ-L-isoleucyl-L-prolyl-L- arginine amide), (BZiPAR)
Rhodamine 110, bis-(succinoyl-L-alanyl-L-alanyl-L- prolyl-L-phenylalanyl amide)
Ac-YVAD-2,6-dimethylbenzoyloxymethylketone
IL-1b Converting Enzyme (ICE) Inhibitor IV
Research use only. The peptides referenced on this page are supplied to qualified laboratories for in-vitro or non-human research. They are not drugs, foods, cosmetics, or dietary supplements, are not for human consumption, and are not intended to diagnose, treat, cure, or prevent any disease. Physicochemical values shown here are transcribed from the cited upstream reference sheet(s); confirm with your own certificate of analysis before use.
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