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¼ÕÀ» Àâ°í °¡¸£ÃÄ ÁÖ´Â DNA Ŭ·Î´× (Á¦3ÆÇ) |
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¡Ø±³È¯ ¹× ¹ÝÇ°¾È³» :
- ±³È¯À̳ª ¹ÝÇ°½Ã »óÇ° ¼ö·ÉÈÄ 3ÀÏÀ̳» ±³È¯À̳ª ¹ÝÇ° Àǻ縦 ¾Ë·ÁÁֽðí ÀÏÁÖÀÏÀ̳»¿¡ ÀúÈñÂÊÀ¸·Î »óÇ°ÀÌ ÀÔ°íµÇ¾î¾ßÇÕ´Ï´Ù. ½ÃÀÏÀÌ °æ°úµÇ¸é ¹ÝÇ°ÀÌ ºÒ°¡ÇÕ´Ï´Ù. - º¯½É¿¡ ÀÇÇÑ ±³È¯À̳ª ¹ÝÇ°½Ã, ¹è¼Ûºñ´Â °í°´´Ô²²¼ ºÎ´ãÇϽøç, ¿À¹è¼ÛÀ̳ª »óÇ° ºÒ·®½Ã¿¡´Â ¹«·á ±³È¯ÀÌ °¡´ÉÇÕ´Ï´Ù. - ¹ÝÇ°½Ã¿¡´Â ¹ÝÇ°»óÇ° °Ë¼öÈÄ Ä«µå Ãë¼Ò¸¦ Çص帮°Å³ª ÅëÀå,Àû¸³±ÝµîÀ¸·Î ȯºÒ Á¶Ä¡ ÇØ µå¸³´Ï´Ù. |
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¡Ø¹è¼Û¾È³» :
- Á¦ÁÖµµ¹× µµ¼»ê°£Áö¿ªÀº Åùèºñ°¡ Ãß°¡µÉ¼ö ÀÖ½À´Ï´Ù. |
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¡¡Restriction enzyme (Á» ´õ Á¤È®ÇÑ ¿ë¾î´Â restriction endonuclease; ¾àÀÚ·Î RE)Àº DNAÀÇ Æ¯Á¤ sequence¸¦ ÀνÄÇÏ¿© À߶óÁÖ¸ç, 1970³â Hamilton Smith (³ªÁß¿¡ ±× °øÀ¸·Î ³ëº§»ó ¼ö»ó)¿¡ ÀÇÇØ Ã³¸§À¸·Î µ¿Á¤µÇ¾ú´Ù.
¡¡REÀÇ ¸í¸íÀº µ¿Á¤µÈ ±ÕÁÖÀÇ À̸§À» µû¸¥´Ù. °¡·É EcoR¥°ÀÇ °æ¿ì Escherichia coli RY13 strain¿¡¼ µ¿Á¤µÇ¾ú´Ù. µû¶ó¼ EcoR¥°ÀÇ Ã³À½ E´Â Escherichia¿¡¼, co´Â coli¿¡¼, RÀº strain À̸§ RY13¿¡¼,¥°Àº ¸ÇóÀ½ µ¿Á¤µÇ¾ú´Ù´Â ÀǹÌÀÌ´Ù. ¸· óÀ½ ½ÇÇè½Ç¿¡ µé¾î¿Í¼ EcoR¥°À» ¡°ÀÌÄھ˾ÆÀÌ¡±¶ó°í Àоú´Ù°¡ ¸Á½Å´çÇÑ ÀûÀÌ ÀÖ´Ù. ¸Ç ¸¶Áö¸· ¡°¥°¡±´Â ¼ýÀÚÀ̹ǷΠ¡°one¡±À̶ó°í Àоî¾ß ÇÑ´Ù. ±×¸®°í °³ÀÎÀÇ ÃëÇâ¿¡ µû¶ó ´Ù¸£±ä ÇÏÁö¸¸, RE¿¡ µû¶ó ÆíÇÏ°Ô Àд ¹æ¹ýÀ» ¼±È£ÇÏ´Â °æ¿ìµµ ÀÖ´Ù. °¡·É Bgl¥±¸¦ ¡°ºñÁö¿¤Åõ¡±´ë½Å¿¡ ¡°º£À̱ÛÅõ¡±¶ó°í Àб⵵ Çϸç, ³ª´Â ¡°º£À̱ÛÅõ¡±·Î Àд ¹æ½ÄÀ» ¼±È£ÇÑ´Ù. Á» ´õ Ä£¼÷ÇÏ°Ô ´À²¸Áö±â ¶§¹®ÀÌ´Ù. »§ÀÌ »ý°¢³ª¹Ç·Î.
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¥°Å¬·Î´×À̶õ?
1.1. Ŭ·Î´×ÀÇ Á¤ÀÇ 17
1.2. »õ·Î¿î À¯ÀüÀÚÀÇ ¹ß±¼ 18
1.3. °ú°ÅÀÇ Å¬·Î´× 20
1.4. ÇöÀçÀÇ Å¬·Î´× 21
¥± Ŭ·Î´×À» À§ÇÑ Áغñ
2.1. Ŭ·Î´× ¼³°è¿¡ À¯¿ëÇÑ ¼ÒÇÁÆ®¿þ¾î 27
2.2. Vector, Plasmid, Construct & Kozak consensus sequence 31
2.3. Multiple Cloning Sites (MCS) 36
2.4. Á¦ÇÑÈ¿¼Ò (Restriction enzyme; RE)¿Í Star activity 39
2.5. Agarose gel electrophoresis for nucleic acids 47
2.6. LB (Luria-Bertani) plate ¸¸µé±â 52
2.7. Competent cells 55
2.8. DNAÀÇ Áú·®À» molar ³óµµ·Î ¹Ù²Ù´Â ¹ý 59
2.9. »õ·Î¿î plasmid¸¦ ¹Þ¾ÒÀ» ¶§ 60
2.10. cDNA library 62
¥² Ŭ·Î´× ù°ÉÀ½
3.1. Cut & Paste 67
3.2. DNA sequencing & Direct sequencing 80
3.3. Ŭ·Î´×À» À§ÇÑ PCR & Nested PCR 85
3.4. Fill-in (Full & Partial) 94
3.5. Compatible cohesive ends 98
3.6. Methylation 100
3.7. Three-piece ligation 109
3.8. Site-directed mutagenesis 112
3.9. ½Ä¹° ÇüÁú Àüȯ (Plant transformation) º¤ÅÍÀÇ ±¸Á¶ 119
3.10. rhizobium radiobacter ÇüÁú Àüȯ 123
¥³ Ŭ·Î´× ´ÙÀ½ °ÉÀ½
4.1. À¯ÀüÀÚ Áß°£ºÎºÐ¿¡ ´Ù¸¥ DNA¸¦ »ðÀÔÇÏ´Â ¹æ¹ý (Insertion)
4.2. À¯ÀüÀÚ Áß°£ºÎºÐÀ» »èÁ¦ÇÏ´Â ¹æ¹ý (Deletion) 131
4.3. À¯ÀüÀÚ¿¡ epitope tagÀ» »ðÀÔÇÏ´Â ¹æ¹ý & CRISPR/Cas9 133
4.4. Translational fusion vs. transcriptional fusion 139
¥´ Ŭ·Î´× ¸¶Áö¸· °ÉÀ½
5.1. ´Ù¸¥ Á¾¿¡¼ À¯»çÇÑ À¯ÀüÀÚ¸¦ cloningÇÏ´Â ¹æ¹ý 143
5.2. RACE (rapid amplification of cDNA ends) 146
5.3. BAC recombineering 149
5.4. Old Trick: partial digestion 153
5.5. º¤ÅÍÀÇ º¯°æ 155
5.6. Ŭ·Î´×ÀÌ ´Ù µÆ´Ù°í »ý°¢Çߴµ¥, frame shift°¡ ÀÖÀ» ¶§ 158
5.7. Ŭ·Î´×ÀÇ ½ÇÁ¦: ¾ï¼¼°Ô ¿îÀÌ ¾ø´Â °æ¿ì 160
¥µ Ŭ·Î´×À¸·Î ÀÎÇÑ µÎÅëÀ» ´ú¾îÁÖ´Â ¹æ¹ý
6.1. TA cloning & T-vectorÀÇ Á¦ÀÛ 173
6.2. TOPO TA cloning 179
6.3. Gateway cloning 182
6.4. Golden gate assembly & Golden gate¸¦ ÀÌ¿ëÇØ Çª´Â Á÷¼ÒÆÛÁñ 185
6.5. In-Fusion Sequence-and Ligation-independent Cloning (In-Fusion SLC) 192
6.6. T4 DNA Polymerase Sequence-and Ligation-Independent Cloning (T4 DNA Pol SLIC) 205
6.7. Non-template PCR cloning 211
¥¶ Cloner¿¡°Ô ÁÖ´Â Á¶¾ð
7.1. Ŭ·Î´×ÀÌ ¾ÈµÉ ¶§ 217
7.2. Ŭ·Î´×ÀÇ Á¤¸®¿Í ±â·Ï 220
Appendix 1. ½ÉÈÇнÀÀ» À§ÇÑ ¹®Çå 224
Appendix 2. ¾àÀÚ 226
Appendix 3. index 228 |
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µî·ÏµÈ ¼ÆòÀÌ ¾ø½À´Ï´Ù. |
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