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VP BF01-1L  ¦è¤è¾¥ÂIªk¾B»\²G - Protein Free ¤H®ð«ü¼Æ 8136
«¬¸¹¡GVP BF01-1L
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­^¤å¦WºÙ¡GBlockPRO™ Protein-Free Blocking Buffer
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BlockPRO ¦è¤è¾¥ÂIªk¾B»\²G Protein-free °t¤è¤£§t³J¥Õ½è¡A ¯à¦³®Ä­°§C¾B»\²G»P³J¥Õ¼Ë¥»ªº¥æ¤¬§@¥Î¡AÁ×§Kª«ºØ¤zÂZ¡CÀ³ ¥Î¼sªx¡A¾A¥Î©ó Western blotting »P ELISA µ¥§K¬Ì¾Ç¹êÅç¡C

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roduct Detail :

Figure 1. BlockPRO™ Protein-Free Blocking Buffer is better than protein-based blocking buffers (skim milk, BSA and casein) for detection of target protein in Western blotting.

THP-1 cell lysates were prepared and separated by electrophoresis. The proteins were transferred to PVDF and blocked for 1 hour at room temperature with the indicated blocking buffer, probed with mouse anti-pAMPK followed by anti-mouse HRP and detected by chemiluminescence. All results were exposed to X-ray film for 30 seconds.

Figure 2. BlockPRO™ Protein-Free is suitable for various protein antigen detection, such as high molecular weight protein, tACC; phosphoprotein, pAMPK; abundant protein, GAPDH; low molecular weight protein, histone H3.

THP-1 cell lysates were prepared and separated by electrophoresis. The proteins were transferred to PVDF and blocked for 1 hour at room temperature with BlockPRO™ Protein-Free Blocking Buffer. Antibodies designed to probe the indicated proteins were used. All the signals were detected by chemiluminescence and were exposed to X-ray film.

Figure  3. BlockPRO™ Protein-Free Blocking Buffer can be used in both PVDF and nitrocellulose platform. 

Hela cell lysates were prepared and separated by SDS-PAGE. The proteins were transferred to PVDF or nitrocellulose membranes. The membranes were blocked for overnight at 4 °C with BlockPRO™ Protein-Free Blocking Buffer or 5% skim milk, probed with mouse anti-histone H3 followed by anti-mouse HRP and detected by chemiluminescence. All results were exposed to X-ray film for 30 seconds.


­qÁʸê°T :

Cat. No. Product Name Description
BF01-1L BlockPRO™ Blocking Buffer

  1 kit  500mL Solution X 2

 

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