BSA-Block

BSA-Block

Product catalog summary
Product Overview: BSA-Block (article no. 115) is a standard blocker used to saturate free binding sites on plastic or other protein-binding surfaces. It is suitable for general laboratory use.
Storage Instructions: Store at 2 – 8 °C or -15 to -30 °C. The product tolerates repeated freezing and thawing cycles.
Specifications: The pH value at 19.0 – 21.0 °C is 7.3 ± 0.2. It contains less than 0.0014% [w/w] of the preservative CMIT/MIT (3:1).
Expiry Date: Refer to the label on the bottle for the expiry date when stored unopened.
Instructions for Use: BSA-Block is ready-to-use and should be shaken thoroughly before use. After immobilizing capture antibodies or antigens, add BSA-Block without dilution to wells or membranes. Incubate at room temperature for 1 - 4 hours or overnight, with 1 hour often being sufficient. Blocking time can be reduced by shaking the plate at 600 - 900 rpm, depending on the application. After blocking, wash the surface to remove BSA-Block before proceeding with the next steps.
Recommendations: The suitability for specific assays and antibodies must be tested by the user. If non-specific binding occurs despite using BSA-Block, consider using The Blocking Solution (article no. 110).
Additional Information: For further details, visit www.candor-bioscience.com.
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Catalog excerpts

BSA-Block-1

Standard blocker for saturating free binding sites on plastic surfaces or other protein binding surfaces Storage: 2 – 8 °C or -15 to -30 °C (tolerates repeated freezing and thawing cycles) contains < 0.0014 % [w/w] reaction mass of CMIT/MIT (3:1) Expiry date when stored unopened: see label on the bottle For general laboratory use Instructions for use BSA-Block is ready-to-use. Please shake the buffer thoroughly before use. After immobilization of capture antibody or antigens, BSA-Block is added without dilution to wells or membranes. Incubate at room temperature for 1 - 4 hours or overnight. 1 hour is often sufficient. Note: The blocking time can be further reduced by shaking the plate at 600 - 900 rpm, depending on the application. The blocking time depends on the properties of the surface to be blocked and the ambient conditions and should therefore be tested. After blocking, the surface is washed to remove BSA-block. The surface (e.g. microtiter plate or blotting membrane) can then be used for the next steps. The suitability for the respective assay and the respective antibodies must be tested by the user. If background occurs due to non-specific binding despite the use of BSA-Block, we recommend the use of The Blocking Solution (article no. 110). For further information please visit www.candor-bioscience.com.

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