Buffers Flashcards
MD037
Feed Media. WFI, Soytone, Yeast Extract, Soy 100, Potassium Phosphate Mono/Dibasic, Dextrose, Ammonium chloride. Soy 100 has high amounts of nucleosides, free amino acids, vitamins, and carbohydrates. Dextrose provides more sugars
MD038
Growth Media. WFI, Soytone, Yeast Extract, Potassium Phosphate Mono/Dibasic, Glycerin
SL060
17% Phosphoric Acid. Fermentation
SL001
Lysis Resuspension Buffer. 50 mM Dextrose, 25 mM Tris, 10 mM EDTA. Tris-EDTA solubilizes nucleic acids and helps protect them from enzymatic lysis. EDTA also binds divalent metals and destabilizes the cell membrane. Dextrose maintains cellular osmolarity to prevent them from bursting
SL002
0.2N NaOH, 1% SDS. SDS solubilizes the phospholipid and protein components of the cell membrane. NaOH denatures plasmid DNA and proteins
SL048
0.4 M NaOH, SL002 component
SL047
2% SDS, component of SL002
SL003
Alkaline Lysis Neutralization Buffer. 3M potassium acetate, 6.75% acetic acid. Causes KDS (potassium dodecyl sulfate), ssDNA, and cell debris to precipitate while allowing p-DNA to renanneal
SL042
Alkaline lysis precipitation buffer. 3.84M CaCl. Helps precipitate RNA
SL017
Used during DEAE equilibration, DEAE wash 2, DEAE elution. ~1.12 M NaCl, 50mM Tris, 10mM EDTA, HCl
SL018
Used during DEAE/HLD equilibration, DEAE wash 1/2, HLD wash 1/2/elution, HLD Resin Strip
SL021
Used for HLD equilibration, loading (diluent), HLD Wash 1/2/elution. 3M ammonium sulfate 50mM Tris, 10mM EDTA
SL019/40
DEAE Resin Strip. 1M NaOH, 2M NaCl. SL040 uses liquids, SL019 uses solids
SL020
20% EtOH, DEAE monolith storage
0.1 M NaOH
HLD monolith storage
Lysis Buffers
- SL001
- SL002 = SL047 + SL048
- SL003
- SL042
1 M NaOH
Chromatography Wash buffer
SL067
Final Formulation Buffer. 10mM Tris, 1mM EDTA, HCL