I-Block™ Protein-Based Blocking Reagent
I-Block™ Protein-Based Blocking Reagent
Invitrogen™

I-Block™ Protein-Based Blocking Reagent

I-Block reagent is a highly purified casein-based blocking reagent. It provides superior blocking compared to both dried milk and BSA.Read more
Catalog NumberQuantity
T201530 g
Catalog number T2015
Price (JPY)
15,600
30 g
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Quantity:
30 g
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I-Block reagent is a highly purified casein-based blocking reagent. It provides superior blocking compared to both dried milk and BSA. Unlike other casein-based blocking reagents, I-Block reagent is essentially biotin-free. I-Block reagent is tested in assays using Tropix substrates and alkaline phosphatase conjugates, and is useful as a blocking reagent in membrane-based and immunoassay applications.

The suggested working concentration is 0.2% (w/v) for detection of nucleic acids on neutral or positively-charged nylon membranes and for immunoassays and protein detection on membranes (nitrocellulose, PVDF, or neutral nylon). For protein detection on positively-charged nylon membrane (such as TropilonPlus membrane), a concentration of 3% is recommended. I-Block blocking solution is prepared in either Tris- or phosphate-buffered saline buffer with heating (40-50°C).

This casein-based blocking reagent can be used with Western-Light, Western-Light Plus, Western-Star, ELISA-Light, Southern-Light, and Southern-Star detection systems.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical Name or MaterialReagent
Recommended StorageStore the product at room temperature.
For Use With (Equipment)Western-Light™ Detection System, Western-Star™ Detection System, Southern-Star™ Detection System, ELISA-Light™ Detection System, Southern-Light™ Detection System, Western-Light Plus™ Detection System
Product LineI-Block, NovaBright
Quantity30 g
Unit Size30 g

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.