SensoLyte® Rh110 Elastase Assay Kit Fluorimetric - 1 kit

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  • Cat.Number : AS-72179
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    In stock
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Elastases catalyze the hydrolysis of elastin, the chief constituent of elastic fibers that together with collagen determines the mechanical properties of connective tissue. Elastases have many other natural substrates these include proteoglycans, collagens and fibronectin. Implicated in many diseases such as pulmonary emphysema, cystic fibrosis, infections, inflammation and atherosclerosis, elastases are considered important drug targets.
The SensoLyte® Rh110 Elastase Assay Kit detects elastase activity using a fluorogenic peptide substrate. Upon elastase cleavage, the peptide releases the Rh110 fluorophore with bright green fluorescence that can be detected at Ex/Em=496 /520 nm. The increase in fluorescence intensity is directly proportional to enzyme activity. The kit does not require any separation steps and can be used to continuously measure the kinetics of elastase. The longer-wavelength spectra and higher extinction coefficient of the Rh110 provide greater sensitivity and less interference from screening compounds.


Kits components
  • Component A: Rh110 Elastase substrate, Ex/Em=490 /520 nm upon cleavage: 2 mM, 50 µL Component B: Rh110, fluorescence reference standard, Ex/Em=490 nm/520 nm: 2 mM, 20 µL Component C: Elastase, porcine pancreas: 10 µg/mL, 100 µL Component D: 2X Assay Buffer: 15 mL Component E: Elastase inhibitor (MeOSuc-Ala-Ala-Pro-Val-CMK): 1 mM, 10 µL
UniProt number
  • P08246
Absorbance (nm)
  • 490
Emission (nm)
  • 520
Storage & stability
Storage Conditions
  • Store all components at -20°C. Protect component A from light and moisture. Component C can be stored at room temperature for convenience.
Biomarker Target
Detection Method
Research Area
Sub-category Research Area
  • Research use
Code Nacres
  • NA.32

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Proteolytic and N-glycan processing of human α1-antitrypsin expressed in Nicotiana benthamiana.

Plant Physiol. . 2014 Oct 25 ; 166(4) 1839 | DOI : 10.1104/pp.114.250720

  • A. Castilho
  • et al