Pierce™ Fast Blocking Buffer
Pierce™ Fast Blocking Buffer
Thermo Scientific™

Pierce™ Fast Blocking Buffer

Pierce Fast Blocking Buffer effectively and reliably blocks western blots in just five minutes to provide low-background results for traditionalRead more
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Catalog NumberQuantity
37576100 mL
37575500 mL
Catalog number 37576
Price (CNY)
1,316.92
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Ends: 31-Dec-2026
1,712.00
Save 395.08 (23%)
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Quantity:
100 mL
Request bulk or custom format
Price (CNY)
1,316.92
飞享价
Ends: 31-Dec-2026
1,712.00
Save 395.08 (23%)
Each
Add to cart
Pierce Fast Blocking Buffer effectively and reliably blocks western blots in just five minutes to provide low-background results for traditional western blotting protocols.

Compare and view all available blocking buffers

Pierce Fast Blocking Buffer streamlines western blot protocols by providing consistent, high-quality blocking for nitrocellulose or PVDF membranes in only five minutes, producing results comparable to traditional blockers. Blocking and probing steps with Fast Blocking Buffer prevent nonspecific binding of detection antibodies during probing steps but allows specific detection to occur. Pierce Fast Wash Buffer provides efficient membrane washing after incubation with a primary and secondary antibody to effectively shorten total washing time to 20 minutes (from the typical 90 minutes). This buffer is compatible with antibodies and biotin-avidin systems, as well as both nitrocellulose and PVDF membranes.

Related products
Pierce Fast Wash Buffer, 10X
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical Name or MaterialBlocking Buffer
Recommended StorageUpon receipt store at 4°C.
Concentration1X
For Use With (Application)Western Blot
Physical FormLiquid
Quantity100 mL
Unit SizeEach

Frequently asked questions (FAQs)

How can I reduce background bands in my Western blot?

Optimize the concentration of primary and secondary antibodies. In some cases, increasing the concentration of blocking agent (BSA or non-fat dry milk) or usiing an alternative blocking solution such as Starting Block or SuperBlock may reduce background signal. After incubation with the primary antibody, wash at least 2 times with TBST (include 0.5 M NaCl in one or more of the wash steps). Avoid Nonidet P40 or Triton X-100 in buffers because protein detection is decreased when these detergents are used.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.