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  InnoZyme™ Insulysin/IDE Immunocapture Activity Assay Kit
Cat. No. CBA079  
All Categories » Calbiochem » Kits and Tools » Protease Assays » Other

Format: 96-well plate
Form: 96 Tests
Detection Method: Fluorescence
Assay Range: 50-1000 ng/ml
Assay Time: 3.5 h
Sample Type: Cell lysates, tissue extracts, biological fluids
Positive Control: Recombinant rat IDE
Kit Contents: Control Rat Recombinant IDE, Anti-Insulysin/IDE Coated 96-Well Plate, Substrate, Assay Buffer, 10X Sample Buffer, Plate Sealer, and a user protocol.
Comments: A specific and sensitive assay for measuring active human, mouse, or rat Insulysin (IDE) in cell lysates, tissue extracts, and biological fluids. IDE is a major enzyme responsible for degrading insulin hence critical for glucose, lipid, and protein metabolism, as well as for cell growth and differentiation. It also plays an important role in both diabetes and Alzheimer's disease.
Ref.: Li, Q., et al. 2006. Cell 127, 305. Shen, Y., et al. 2006. Nature 443, 870. Song, E.S. and Hersh, L.B., 2005. J. Mol. Neurosci. 25, 201. Farris, W., et al. 2003. PNAS USA 100, 4162. Morelli, L., et al. 2003. J. Biol. Chem. 278, 23221. Song, E.S., et al. 2001. J. Biol. Chem. 276, 1152.

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EMD Chemicals Inc. USD list price is displayed (pricing with local distributors may vary). NOTE: In Stock status is based on item availability worldwide.

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1 kit*$536.00

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Cat. No.Disclaimers
CBA079-1KIT
Stock StatusPlease contact our Customer Service Department for delivery time.


Activity of recombinant rat and human IDE.. Recombinant rat and human IDE activity was measured as outlined in the Detailed Protocol above using a 4-h incubation at 37°C. The data is presented as Relative Fluorescence Units.


IDE Activity in Cell Lysates and Tissue Extracts. IDE Activity in Biological Samples. Cells (cell types are denoted in the figure) were cultured in DMEM or RPMI medium supplemented with 10% FCS and harvested at 80-90% confluency. Total cell lysates were prepared using CytoBuster™ Protein Extraction Reagent (Cat. No. 71009) according to the manufacturer's recommended protocol. Human spleen extract was prepared by homogenizing tissue in 170 mM NaCl and 2 mM EDTA. Protein concentration was determined using a BCA protein assay. Activity was assessed as outlined in the Detailed Protocol above. Fluorescence intensity was measured at an excitation wavelength of 320 nm and an emission wavelength of 405 nm and expressed per mg total protein.

Related Literature:

Diabetes and Obesity Brochure

Biologics 33.2

Novagen inNovations Newsletter 27

Material Safety Data Sheets:
CBA079: InnoZyme™ Insulysin/IDE Immunocapture Activity Assay Kit - English
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All Categories » Calbiochem » Kits and Tools » Protease Assays » Other