Molecular biology

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	#[http://www.strgen.org/protocols/lic-vector-prep.pdf Vector preparation]		#[http://www.strgen.org/protocols/lic-vector-prep.pdf Vector preparation]
	#[http://www.strgen.org/protocols/lic-insert-prep.pdf Insert preparation]		#[http://www.strgen.org/protocols/lic-insert-prep.pdf Insert preparation]
-	#[http://www.strgen.org/protocols/lic-rxn-transf.pdf LIC transformation]	+	#[http://www.strgen.org/protocols/lic-rxn-transf.pdf LIC transformation]:
		+	##mix insert and vector in appropriate amounts
		+	##incubate 5~30 min(20 min) at room temperature
		+	##do transformation in E. coli (recommend to use electro-competent cells)
		+
	==Softwares==		==Softwares==
	#[[NIH Image]]: Gel analysis software		#[[NIH Image]]: Gel analysis software

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Revision as of 06:43, 9 July 2008

Contents 1 Reagents & Protocols 1.1 recipes 1.2 protocols 2 Softwares

Reagents & Protocols

recipes

1. Commonly used reagents and equipment in molecular biology (PDF)
2. Concentration of antibiotics commonly used

protocols

1. PCR - General rules for primer design
2. Genomic DNA extraction
3. Competent cell preparation BSGC protocol (PDF)
4. Electrocompetent cell Protocol (PDF)
5. LIC cloning introduction LIC introduction - Ligation Independent Cloning

• LIC cloning protocol (Berkeley Structural Genomics Center)

1. Vector preparation
2. Insert preparation
3. LIC transformation:
   1. mix insert and vector in appropriate amounts
   2. incubate 5~30 min(20 min) at room temperature
   3. do transformation in E. coli (recommend to use electro-competent cells)

Softwares

1. NIH Image: Gel analysis software
2. Serial Cloner: DNA sequence management (PCR, restriction maps, etc.)
3. Bioedit
4. BioX (Mac OS X only)