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407207  SignalBoost™Immunoreaction Enhancer Kit

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Merck KGaA
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29 May 2012

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Product number Qty/Pk Quantity Price
407207-1KIT  1 kit  loading
Prices are subject to change without notice.
SignalBoost™ Immunoreaction Enhancer Kit is designed to enhance the desired signal in assays such as immunoblotting, dot blotting, and ELISA. This kit significantly improves sensitivity and discrimination when assessing protein targets of low immunoreactivity or low expression levels. Enhancement of signal is especially marked for low affinity antibodies. It replaces conventional antibody diluents with Solution 1, which is used to dilute primary antibodies and Solution 2, which is used to dilute secondary antibodies. No additional steps, materials, or increase of assay time is required.

Increases signal: minimizes background resulting in high signal to noise ratios
Versatile: can be used with nitrocellulose or PVDF membranes and is compatible with chemiluminescent or colorimetric detection systems
Convenient: ready-to-use format, no dilution necessary
Product information
Format Liquid, Antibody Diluent
Form 20 Miniblots or 1600 cm2
Detection method Chemiluminescence, colorimetric, or fluorescence
Protect from Light Yes
Kit contains Solution 1 for Primary Antibodies, Solution 2 for Secondary Antibodies, and a user protocol.
Store and ship information
Storage +2°C to +8°C
Ship Blue Ice Only
Standard Handling
Data

Detection of protein kinase C by immunoblotting. Samples: whole cell lysate from K562 cells. Immunoblotting conditions: nitrocellulose membrane blocked overnight with 5% milk in PBST; all washes were performed with PBST. Primary antibody: Anti-PKC (Ab-2) Mouse mAb (MC5) (Cat. No. OP74) diluted 1:1000 in 5% milk/PBST (lane A) or in Solution 1 (lane B) (incubation for 1 h ). Secondary antibody: Anti-Mouse IgG diluted 1:10,000 in 5% milk/PBST (lane A) or Solution 2 (lane B). Detection: chemiluminescence (30 s exposure).

ELISA results generated with and without dilution of antigen and detection antibody using SignalBoost™ reagent.

© Merck KGaA, Darmstadt, Germany, 2012


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