Neutrophil Elastase on the ASK
- Products and catalog numbers
- Using Neutrophil Elastase in vivo/ex vivo
- Application notes and posters
Neutrophil elastase is a key protease involved in acute lung injury, acute respiratory distress syndrome, as well as many other inflammatory processes such as emphysema, cystic fibrosis, COPD, wound healing, rheumatoid arthritis, and ischemia-reperfusion. Neutrophil Elastase 680 FAST™ is a fluorescent agent that is selectively cleaved by elastase produced by activated neutrophils during acute inflammation. Neutrophil Elastase 680 FAST is optically silent upon injection and produces fluorescent signal only after cleavage by elastase.
Neutrophil Elastase 680 FAST is a member of a family of activatable fluorescent imaging agents comprising a novel architecture, termed F.A.S.T. (Fluorescent Activatable Sensor Technology) that confers an improved pharmacokinetic profile with a broader range of early imaging time points. This architecture also offers higher target specific signal with reduced background. Neutrophil Elastase 680 FAST can be used for imaging both in vitro and in vivo.
Neutrophil Elastase 680 FAST enables imaging of neutrophil elastase activity in applications including:
- Acute lung injury models
- Acute respiratory distress syndrome
- Cystic Fibrosis
- Wound Healing
- Rheumatoid Arthritis
Products and catalog numbers
|Product||Catalog Number||Ex/Em wavelength (nm)||Molecular weight (g/mol)||Validated Experiments||Applications||Storage and Stability|
|Neutrophil Elastase 680 FAST||NEV11169||675/693||43,000||In vivo/Ex vivo||Acute inflammation|
|Technical Data Sheet|
Using Neutrophil Elastase 680 FAST in vivo/ex vivo
The generally recommended procedure for in vivo imaging with Neutrophil Elastase 680 FAST is administration via intravenous injection and imaging 4-8 hours post injection. Earlier and later time points may be appropriate for some disease models, and the optimal imaging time point for any application should be determined empirically.
|Product||Route of Injection||Mouse Dose (25 g)||Rat Dose (250 g)||Blood t 1/2||Tissue t 1/2||Optimal imaging time||Optimal Re-injection Time (complete clearance)||Route of Metabolism/ background tissue||FMT& IVIS settings|
|Neutrophil Elastase 680 FAST||IV||4 nmol||12-40 nmol||3 h||12 h||3-6 h||2 d||Bladder, liver, intestines||FMT 680/700
Figure 1: Paw inflammation was induced with carageenan (CG) injection. CG-injected mice were measured for changes in paw thickness, vascular leak (AngioSense® 750EX), neutrophil elastase activity (Neutrophil Elastase 680 FAST), and cathepsin activity (Cat B 680 FAST) by injecting these agents at two time points, 2h (early) and 24h (late), post CG injection. Tomographic (3D) paw imaging was performed on the FMT2500 5h after agent injection. All CG-induced responses were statistically significant at both time points (p < 0.01), revealing significant recruitment of inflammatory cells.
Frozen Tissue Protocol
We have validated Neutrophil Elastase 680 FAST for use with frozen tissue samples. Here is a brief protocol with a recommended concentration of agent to use:
- Freeze tumor (without agent) and section 5-10 µm by cryostat. For lung samples, mice are challenged intranasally with 100 µg of LPS followed by intranasal instillation of 200 nM fMLP in 40 uL PBS 18 h later. Harvest lungs 5 h later. For specificity, co-incubate agent with Silvelestat inhibitor.
- Incubate with 1 uM Neutrophil Elastase 680 FASTat 37ºC for 10-30 min for tumors; 5 h for lungs.
- Wash 1x with PBS.
- Mount with anti-fade reagent.
- Fluorescence microscopy filter: Cy5.5
Application notes and posters
- Poster: A novel NIR dye for in vivo temporal tracking of labeled macrophages to sites of acute inflammation
- Poster: Near-Infrared Quantitative Fluorescence Imaging of Renin Activity in Kidney Tissue
Please visit our Citations Library for references using Neutrophil Elastase 680 FAST on the IVIS or on the FMT.