Polymerase Chain Reaction (PCR) to Amplify rRNA Gene Fragment
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<center> <b><font>Polymerase Chain Reaction (PCR) to Amplify rRNA Gene Fragment</font> </b></center>
- 
		Prepare sufficient master mix for both partners (45 mL/50 mL reaction) 
		- 10 mL 10x PCR buffer
- 10 mL 2.5 mM dNTPs (0.25 mM final concentration)
- 15 mL Primer A (5 pmole/mL)
- 15 mL Primer B (5 pmole/mL)
- 40 mL H2 O
- 0.4 mL TaKaRa Ex-Taq DNA Polymerase (2 units)( Panvera )
- 
				90 mL
 
 
 
- 
		Aliquot 45 mL of master mix into each of two 0.5 mL microfuge tubes labelled with the student's initials; PCR; date.
 
 
- 
		Add 1-5 mL template DNA1 (100 ng for bacterial genomic DNA), 0-4 mL H2 O to yield a final volume of 50 mL.
 
 
- 
		Add 50 mL mineral oil (using cut pipette tip), close tube tightly, place in thermal cycler.
 
 
- Initiate thermal cycling program.
- 
	Phase 1 - 1 cycle
	
- 
		- Initial denaturation 4 min. @ 94o C
- Primer annealing 45 sec. @ 55o C
- Primer extension2 1 min. @ 72o C
 Phase 2 - 35 cycles
- 
		- standard denaturation 1 min. @ 94o C
- Primer annealing 45 sec. @ 55o C
- Primer extension2 1 min. @ 72o C
 Phase 3 - 1 cycle
- 
		- standard denaturation 1 min. @ 94o C
- Primer annealing 45 sec. @ 55o C
- Primer extension2 10 min. @ 72o C
 
1 To improve specificity, template DNA concentration, annealing temperature and Mg2+ concentration may be varied.
2 1 minute extension time should be used for each kbp of product expected.
PCR方法相关产品:
- 电泳设备
- 紫外设备
- 普通PCR仪
- 定量PCR仪
- 
		PCR/RT-PCR/qPCR试剂
- 
		PCR引物
- 
		PCR试剂
- 
		PCR对照
- 
		特异性PCR试剂盒
- 
		PCR克隆试剂盒
- 
		RNA
- 
		RNase检测/去除
- 
		RT-PCR试剂
- 
		RT-PCR标准品
- 
		定量PCR试剂
- 
		定量PCR标记
- 
		总RNA分离纯化盒
- 
		PCR产物纯化
- 
		核酸酶
- 
		聚合酶
- 
		反转录酶










