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      * ÇØ´ç ½Ã¾àÀº ÁÖ·Î ³ó¾÷¿¡¼­ Á¦ÃÊÁ¦·Î »ç¿ëµÇ¸ç, À¯ÀüÀÚ º¯Çü ÀÛ¹°ÀÇ ¼±ÅÃÀû Á¦ÃÊÁ¦ ¿ªÇÒÀ» ÇÕ´Ï´Ù. bar ¶Ç´Â pat À¯ÀüÀÚ°¡ µµÀÔµÈ ½Ä¹°À» ¼±ÅÃÇÏ´Â µ¥ »ç¿ëµÇ¸ç, ºñÀ¯ÀüÀÚ º¯Çü ÀÛ¹°¿¡µµ ¿µÇâÀ» ¹ÌÄ¡¹Ç·Î ÁÖÀÇÇÏ¿© »ç¿ëÇØ¾ß ÇÕ´Ï´Ù.

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      PPT [MB-P4691]

       

       

       

      INSTRUCTION

       

      À̸í

      DL-Phosphinothricin, Be able to replaced by Bialaphos

      È­ÇнÄ

      C5H15N2O4P

      ºÐÀÚ·®

      198.2

      CAS No.

      77182-82-2

      º¸°ü¿Âµµ

      Room Temperature

      ¿ë¸Å

      Soluble in Water

      * ÇØ´ç Á¦Ç°Àº ½Ä¹° Á¶Á÷¹è¾ç ¹× ¹Ì»ý¹°½ÇÇèÀ» À§ÇØ »ç¿ëµÇ´Â ½Ã¾àÀÔ´Ï´Ù.

       

       

       

      PACKAGE

       

      Quantity

      Cat. No

      250mg

      MB-P4691-250mg

      1g

      MB-P4691-1g

       

       

       

      Reference

      Leung H., Pat Loomis, and Martin L. Pall. ¡°Transformation of Magnaporthe grisea to phosphinothricin resistance using the bar gene from Streptomyces hygroscopicus.¡± Department of Plant Pathology, Washington State University, Pullman, WA 99164-6430.

      <http://www.fgsc.net/fgn42/leung.html> Accessed: [10/31/2011 2:12:16 PM].

      Schwartz D, S. Berger, E. Heinzelmann, K. Muschko, K. Welzel, and W. Wohlleben (2004) Biosynthetic Gene Cluster of the Herbicide Phosphinothricin Tripeptide from Streptomyces viridochromogenes Tu494. Applied And Environmental Microbiology 70:12 Pp. 7093–7102

       Schwartz D, N. Grammel, E. Heinzelmann, U. Keller and W. Wohlleben (2005) Phosphinothricin Tripeptide Synthetases in Streptomyces viridochromogenes Tu¡§494. Antimicrobial Agents And Chemotherapy, 49:11, Pp. 4598–4607.

       

       

       

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