∙ 1Amino Acid Titration
°¡. Amino AcidÀÇ ampholytes ·Î¼ÀÇ ¼ºÁú
³ª. Henderson-Hasselbalch Equation
´Ù. Amino AcidÀÇ Titration°ú pH buffer ÀÛ¿ë
¶ó. ¿©·¯°¡Áö Amino AcidÀÇ »ê-¿°±â ¼ºÁú
¸¶. Amino Acid TitrationÀÇ ÀÇÀÇ
∙ Protein Á¤·®ºÐ¼® (ºä·¿¹ý/·Î¿ì¸®¹ý)
°¡. Protein Á¤·®ÀÇ °³¿ä
³ª. ÁÖ¿äÇÑ Protein Á¤·®¹ý
´Ù. SpectrophotometryÀÇ ±âº» ¿ø¸®
∙ Protein Seperation & Purification
°¡. Protein Seperation ¿¡ »ç¿ëµÇ´Â ±âº» ¿ø¸®
³ª. ´Ü¹éÁú ÃßÃâ
´Ù. ´Ü¹éÁúÀÇ Á¤Á¦¹ý
∙ SDS-PAGE
°¡. ElectrophoresisÀÇ ±âº» ¿ø¸®
³ª. ºÒ¿¬¼Ó °Ö Àü±âÀ̵¿¹ý (Disc-gel Electrophoresis) ¹ý
´Ù. SDS-Gel Electrophoresis
¶ó. Acrylamide Gel Á¦Á¶¿¡ »ç¿ëµÇ´Â Agent
∙ Enzyme Assay
°¡. Enzyme°ú inorganic Catalytic Agent¿ÍÀÇ Â÷ÀÌÁ¡ / °øÅëÁ¡
³ª. EnzymeÀÇ Substrate Specitify
´Ù. Enzyme KineticsÀÇ ÀÇÀÇ
¶ó. Michealis-Menton ½Ä°ú Km, Vmax ÀÇ ÀǹÌ
¸¶. Lineweaver-Bulk Plot
¹Ù. Inhibition°ú Michealis-Menton Equation
»ç. Enzyme ¹ÝÀÀ ¼ÓµµÀÇ ÃøÁ¤¹ý
∙ The Preparation of Genomic DNA & Plasmid DNA from Bacteria
°¡. Agarose gel Electrophoresis
∙ Bacterial Transformation
°¡. Transformation
³ª. Simple Transformation
´Ù. Eliminating Restriction System of E.Coli
∙ Physical Properties of DNA
°¡. Denaturation and Melting Curve of DNA
³ª. Double-Helix DNAÀÇ Stability¿¡ ¿µÇâÀ» ¹ÌÄ¡´Â Factorµé
´Ù. Renaturation and C0t Value
¶ó. Hyperchromic Effect & C+G ratio Estimation
¸¶. Diphenylamine ºÐ¼®¹ý¿¡ ÀÇÇÑ DNAÀÇ Á¤·®
∙ Southern Blotting
°¡. Blotting Technique
³ª. Prototype of Sourthern Blotting
´Ù. ECL Method
¶ó. Trp ED Gene
∙ Carbohydrate Á¤¼ººÐ¼®
°¡. CarbohydrateÀÇ ±âº» ±¸Á¶
³ª. CarbohydrateÀÇ Á¤¼ººÐ¼®¹ý