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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
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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
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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
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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
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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