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 Á¦Ç°¾È³»  Àü±â¿µµ¿  ´Ü¹éÁú Àü±â¿µµ¿  Western Blot Kit

Luminata Western HRP substrate

Western blot ÈÄ, ¹ß»ö¿¡ »ç¿ëµÇ´Â premixed ECL solution ÀÔ´Ï´Ù.

Millipore
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  • Luminol°ú Peroxidase solutionÀÌ 1:1·Î ¼¯ÀÎ premixed ÇüÅ¿©¼­ »ç¿ëÀÌ Æí¸®Çϸç, ½Ã¾àÀ» È¥ÇÕÇÒ¶§ ¹ß»ýÇÒ ¼ö ÀÖ´Â cross contaminationÀ» ¹æÁöÇÕ´Ï´Ù.
  • Detection range¿¡ µû¶ó 3°¡Áö Á¦Ç°Áß ¿øÇϽô Á¦Ç°À» ¼±ÅÃÇÏ¿© »ç¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
  • SNAP id system¿¡ validationµÇ¾ú½À´Ï´Ù.
  • pipetting error¸¦ ÃÖ¼ÒÈ­ ÇÏ¿© °á°ú°¡ ÀÏÁ¤ÇÕ´Ï´Ù.
  • »ó¿ÂÀ̳ª 4¡É¿¡¼­ 1³â°£ ¾ÈÁ¤ÇÕ´Ï´Ù.
  • °¡Áö°í °è½Ã´Â PVDF³ª nitrocellulose membrane¿¡ ȣȯÀÌ °¡´ÉÇÕ´Ï´Ù.
    Á¦Ç°ÀÇ Á¾·ù
  1. Luminata Classico: °¡Àå ÀϹÝÀûÀ¸·Î »ç¿ëÇÒ ¼ö ÀÖ´Â Á¦Ç°ÀÔ´Ï´Ù.
  2. Luminata Crescendo: ³·Àº picogram¹üÀ§±îÁö °ËÃâ ÇÒ ¼ö ÀÖ´Â Á¦Ç°ÀÔ´Ï´Ù.
  3. Luminata Forte: femtogram ¹üÀ§¸¦ °ËÃâ ÇÒ ¼ö ÀÖ´Â Á¦Ç°ÀÔ´Ï´Ù.
Three different sensitivities of Luminata substrates meet all detection needs
Detection of GAPDH in 10 ¥ìg (Lane 1), 5 ¥ìg (Lane 2), 2.5 ¥ìg (Lane 3), and 1.2 ¥ìg (Lane 4) of A431 lysate. Blots were treated with the indicated detection substrate and exposed to x-ray film for 5 minutes. Luminata Forte substrate is equivalent to Immobilon Western Chemiluminescent HRP Substrate (WBKLS0500, Millipore).
    »ç¿ë¿¹
    Premixed Luminata substrate signals stay strong even after long term storage
    Dilution series of stimulated A431 lysates (10-0.6 ¥ìg) were resolved by SDS-PAGE then transferred on to Immobilon P membrane (Millipore). Blots were blocked with Bl©ªk-CH reagent (Millipore) and probed with either anti-PP2, anti-STAT1 (05-987, Millipore), or anti-BRCA1 (05-842, Millipore) primary antibody diluted in Bl©ªk-CH reagent. The appropriate secondary antibodies were added to each antibody. Each blot was visualized with indicated HRP detection reagent. Blots processed using the SNAP i.d. protein detection system (Millipore).