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GC-rich Template¿¡ °­ÇÑ High Fidelity PCR È¿¼Ò

HS with GC Buffer

-

Á¦Á¶»ç Á¦Ç°ÄÚµå Á¦Ç°¸í ¿ë·® °¡°Ý
(ºÎ°¡¼¼º°µµ)
ºñ°í »ç¿ëÀڸŴº¾ó
Takara
R044A
PrimeSTAR¢ç HS DNA Polymerase with GC Buffer
°ü·ÃÇмú ±¸¸ÅÇϱ⠶óÀ̼±½º 
250 U
264,000¿ø  R044A.e_v1908Da.pdf
Takara
R044B
PrimeSTAR¢ç HS DNA Polymerase with GC Buffer
°ü·ÃÇмú ±¸¸ÅÇϱ⠶óÀ̼±½º 
1,000 U (R044A x 4)
848,000¿ø 

Á¦Ç°¼³¸í
PrimeSTAR HS DNA Polymerase´Â, ´ÙÄ«¶ó¹ÙÀÌ¿À°¡ µ¶ÀÚÀûÀ¸·Î °³¹ßÇÑ Áö±ØÈ÷ ³ôÀº Á¤È®¼º°ú ¶Ù¾î³­ ÁõÆø È¿À²À» °âºñÇÏ´Â DNA polymeraseÀÌ´Ù. º» È¿¼Ò´Â ¸Å¿ì °­·ÂÇÑ 3' - 5' exonuclease È°¼ºÀ» °¡Á®, PCR ÁõÆø¿¡ ´ëÇØ °­·ÂÇÑ Proofreading ±â´ÉÀ» ³ªÅ¸³»´Â ÇÑÆí, Taq DNA PolymeraseÀÇ ¸Å¿ì ¶Ù¾î³­ ÁõÆø È¿À²µµ ³ªÅ¸³½´Ù. »ó¿Â¿¡¼­ÀÇ DNA Polymerase È°¼º ¹× 3' - 5' exonuclease È°¼ºÀ» ¾ïÁ¦ÇÏ´Â monoclonal Ab¸¦ ÷°¡ÇÏ°í Àֱ⠶§¹®¿¡, PCR ¹ÝÀÀÀüÀÇ miss-primingÀ̳ª primerÀÇ digestionÀ» ¸·À» ¼ö ÀÖ¾î ³ôÀº ¹ÝÀÀ ƯÀ̼ºÀ» ¾òÀ» ¼ö ÀÖ´Ù.¶Ç, º» È¿¼Ò´Â ³ôÀº priming È¿À²À» °¡Áö°í Àֱ⠶§¹®¿¡, annealing ½Ã°£À» ª°Ô ¼³Á¤ÇÒ ¼ö ÀÖ¾î Á¾·¡ÀÇ ¹ÝÀÀ ½Ã°£À» ´ÜÃàÇÒ ¼ö ÀÖ´Ù. °Ô´Ù°¡ °íµµ·Î ÁöÀûÈ­ÇÑ PrimeSTAR Buffer¸¦ ÀÌ¿ëÇÏ´Â °ÍÀ¸·Î, Æø³ÐÀº Ÿ°Ù¿¡ ´ëÇØ High Fidelity, °í°¨µµ, °íƯÀ̼º, ³ôÀº ¼º°øÀ²·Î ÁõÆøÀÌ µÇ¾ú´Ù.
Ư¡
GC richÀÎ Thermus thermophilus HB8 genomic DNA¸¦ ÁÖÇüÀ¸·Î¼­ ÀÓÀÇ¿¡ ¼±ÅÃÇÑ 8 ¿µ¿ª(ÁõÆø »çÀÌÁî´Â °¢°¢ ¾à 500 bp)À» PCR ÁõÆø ÈÄ, º¤ÅÍ¿¡ Ŭ·Î´× ÇØ, °¢ ¹è¿­¿¡ ´ëÇØ º¹¼ö Ŭ·ÐÀ» ÇȾ÷ ÇØ ±× ¼ø¼­¸¦ È®ÀÎÇØ, mutation frequency¸¦ ¾ò¾ú´Ù.
±× °á°ú, PrimeSTAR HS DNA Polymerase´Â Taq DNA Polymerase¿Í ºñ±³Çؼ­ 10¹è Fidelity°¡ ³ô°í, A»ç High Fidelity È¿¼Ò¿¡ ºñÇصµ µ¿µî ÀÌ»óÀÇ Á¤È®¼ºÀ» ³ªÅ¸³Â´Ù.
ÀÌ ¹æ¹ýÀº, ½ÇÁ¦ÀÇ PCR¿¡ °¡Àå Á¤È®ÇÏ°Ô FidelityÀÇ ±¸ÇÏ´Â ¹æ¹ýÀ̸ç, Á¤È®¼ºÀÌ Áß¿äÇÑ ¹ÝÀÀ¿¡ ¾È½ÉÇÏ°í º»È¿¼Ò¸¦ »ç¿ëÇÒ ¼ö ÀÖ´Ù.
³»¿ë(250U)
PrimeSTAR HS DNA Polymerase with GC buffer (TaKaRa Code R044A/B)
PrimeSTAR HS DNA Polymerase(2.5 U/ul) 100 ul
2 x PrimeSTAR GC Buffer(Mg2+Plus) 1.7 ml x 3
dNTP Mixture(2.5 mM) 800 ul
* Mg2+ ³óµµ:5 mM (5¡¿)
ÇüÅÂ
50 mM Tris-HCl(pH8.2 at 4¡É)
100 mM NaCI
0.1 mM EDTA
1 mM DTT
0.1 % Tween 20
0.1 % Nonidet P-40
50 % Glycerol
È°¼ºÀÇ Á¤ÀÇ
È°¼ºÈ­ salmon sperm DNA¸¦ Template/primer·Î ÀÌ¿ëÇØ ¾Æ·¡¿Í °°Àº È°¼º ÃøÁ¤¿ë ¹ÝÀÀ¾× Áß¿¡¼­ 74¡É¿¡¼­ 30ºÐ°£ 10 nmolÀÇ nucleotides¸¦ acid insolubility sediment·Î Àüȯ½ÃÅ°´Â È°¼ºÀ» 1 U·Î ÇÑ´Ù.
È°¼º ÃøÁ¤¿ë ¹ÝÀÀ¾× Á¶¼º
100 mM Tris-HCl ¿ÏÃæ¾× pH8.3 at 37¡É
10 mM KCl
6 mM (NH4)2SO4
2 mM MgCl
0.1 % Triton X-100
0.001£¥ BSA
°¢ 200 ¥ìM dATP¡¤dGTP¡¤dCTP
100 ¥ìM [3H£ÝTTP
0.4 mg/mll È°¼ºÈ­ salmon sperm DNA
PCR »ê¹°
PrimeSTAR¢ç HS DNA Polymerase¸¦ ÀÌ¿ëÇØ ÁõÆøÇÑ PCR »ê¹°ÀÇ ´ëºÎºÐÀº ÆòÈ° ¸»´Ü (Blunt End)ÀÌ´Ù.
µû¶ó¼­ T-vector¿¡ Ŭ·Î´× ÇÏ´Â °æ¿ì, PCR »ê¹°ÀÇ 3' ¸»´Ü¿¡ dA¸¦ ºÎ°¡ÇØ¾ß Çϸç, Mighty TA-cloning Reagent Set for PrimeSTAR¢ç(Code 6019)¸¦ ÀÌ¿ëÇÏ¿© A-tailing ¹× TA cloningÀ» ÁøÇàÇÒ ¼ö ÀÖ´Ù.
PCR »ê¹°À» ±×´ë·Î (ÇÊ¿ä¿¡ µû¶ó¼­ ÀλêÈ­ÇÏ¿©) ÆòÈ° ¸»´Ü º¤ÅÍ¿¡ Ŭ·Î´×ÇÏ´Â °æ¿ì Mighty Cloning Reagent Set (Blunt End) (Code 6027)¸¦ ÀÌ¿ëÇÒ ¼ö ÀÖ´Ù.
PCR °ËÁ¤
- ¥ëDNA¸¦ ÁÖÇüÀ¸·Î ÇÑ PCR(ÁõÆø »ê¹° 8, 10, 12, 15 kbp)¿¡ ´ëÇØ ¾çÈ£ÇÑ ÁõÆøÀ» º¼ ¼ö ÀÖ´Â °ÍÀ» È®ÀÎÇÏ°í ÀÖ´Ù.
- Human genome DNA¸¦ ÁÖÇüÀ¸·Î ÇÑ PCR(ÁõÆø »ê¹° 0.5, 1, 2, 4, 6, 8 kbp)¿¡ ´ëÇØ ¾çÈ£ÇÑ ÁõÆøÀ» º¼ ¼ö ÀÖ´Â °ÍÀ» È®ÀÎÇÏ°í ÀÖ´Ù
º¸Á¸ -20¡É
¼øµµ
- 10 UÀÇ º» È¿¼Ò¿Í 0.6 ¥ìgÀÇ ¥ë-Hind III ºÐÇع°À» 74¡É, 1½Ã°£ ¹ÝÀÀ½ÃÄѵµ DNAÀÇ Àü±â ¿µµ¿ ÆÐÅÏ¿¡ º¯È­´Â ÀϾÁö ¾Ê´Â´Ù.
- 10 UÀÇ º» È¿¼Ò¿Í 0.6 ¥ìgÀÇ supercoiled pBR322 DNA¸¦ 74¡É, 1½Ã°£ ¹ÝÀÀ½ÃÄѵµ DNAÀÇ Àü±â ¿µµ¿ ÆÐÅÏ¿¡ º¯È­´Â ÀϾÁö ¾Ê´Â´Ù.
°ü·ÃÁ¦Ç°
- A-tailing & TA cloning kit: Mighty TA-cloning Reagent Set for PrimeSTAR¢ç
- 15ºÐ ¿Ï·á! ¿øÁ¶ PCR cloning kit: In-Fusion¢ç Snap Assembly Master Mix
- Á¤È®ÇÑ cDNA ÇÕ¼ºÀ» À§ÇÑ ¿ªÀü»ç¹ÝÀÀ kit: PrimeScript¢â II 1st strand cDNA Synthesis Kit
- Gel elution¿ë Agarose: SeaPlaque¢ç Agarose
- ÄÄÆÑÆ®ÇÑ 96 well gradient PCR ±â±â: Clontech PCR Thermal Cycler GP

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