Table of Contents (Ver. 2.24.18)
I. Basic Experiments
- DNA digestion
- DNA Ligation-1: User specified vector/insert ratio.
- DNA Ligation-2: Automatically calculate the vector/insert ratio.
- DNA Ligation-3: Automatically provide the range of vector/inset ratio from 1/1 to 1/5.
- DNA Assembly
II. Normalisation
- Normalisation by mass
- Normalisation by molecules
- Normalisation by cells
III. Conversion
- OD260 to mass
- OD260 to moles
- Mass to moles
- Moles to mass
- RPM to RCF
- RCF to RPM
IV Physical quantities
- DNA physical quantities
- RNA physical quantities
V. Melting temperature
- Perfect matched DNA oligos
- Mismatched DNA oligos
- DNA oligos with inosines
VI. Plasmid, Cosmid, Phage
- Plasmid copy number
- Cosmid in vivo packaging
- Expected cosmid packaging efficiency
- Phage multiplicity of adsorption: Considering adsorption rate to evaluate multiplicity of infection (MOI).
VII. Bacterial growth
- Culture tracking
- OD alarm timer: Alert when the culture reaches the desired growth level.
- Fitness cost
- Conjugation rate
VIII. Lab strain references
- Selection antibiotics
- Genotypes
- Common markers
- Genes and products
- Essential genes
IX. Restriction enzymes
- Find recognition sequences
- Find Type IIP enzymes
- Find Type IIS enzymes
- Codon and enzymes
- Palindromic compatible ends