Pierce Protein-Free Blocking Buffer is a non-protein compound that provides effective blocking for membrane-based and plate-based protein detection methods, resulting in extremely low background.
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Catalog Number
Quantity
Buffer
37571
1 L
TBST
37584
100 mL
PBS
37572
1 L
PBS
37585
100 mL
TBS
37570
1 L
TBS
37573
1 L
PBST
6 Options
Catalog number 37571
Price (USD)
262.65
Online Exclusive
288.00
Save 25.35 (9%)
Each
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Quantity:
1 L
Buffer:
TBST
Request bulk or custom format
Price (USD)
262.65
Online Exclusive
288.00
Save 25.35 (9%)
Each
Add to cart
Pierce Protein-Free Blocking Buffer is a non-protein compound that provides effective blocking for membrane-based and plate-based protein detection methods, resulting in extremely low background. It is supplied in a convenient, ready-to-use format.
Features of Protein-Free Blocking Buffer include: • Protein-free blocker—minimizes or eliminates cross-reactivity associated with protein-based blocking buffers • Applications—compatible with western blotting (membranes), ELISA (microplates), and arrays (coated glass slides) • Streptavidin-friendly—free of biotin; no interference with avidin-biotin detection systems • High-performance—optimized and validated in many protein methods to provide high signal-to-noise ratio (i.e., no quenching of specific binding and signal but eliminating nonspecific binding and background)
Traditional blocking buffers contain proteins that can cross-react in certain immunodetection systems, resulting in high background and reduced signal. Pierce Protein-Free Blocking Buffers are devoid of protein while remaining highly effective at blocking plates, membranes, and other surfaces for ELISA, western blotting, glass slide arrays, and other applications.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Blocking AgentNon-protein compound
BufferTBST
Concentration1X
For Use With (Application)ELISA, Western Blot
FormLiquid
Product LinePierce™
Product TypeBlocking Buffer, protein-free
Quantity1 L
Unit SizeEach
Contents & Storage
Upon receipt store product at room temperature. After opening, store product at 4°C.
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.