Buffers Flashcards

1
Q

MD037

A

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

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2
Q

MD038

A

Growth Media. WFI, Soytone, Yeast Extract, Potassium Phosphate Mono/Dibasic, Glycerin

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3
Q

SL060

A

17% Phosphoric Acid. Fermentation

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4
Q

SL001

A

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

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5
Q

SL002

A

0.2N NaOH, 1% SDS. SDS solubilizes the phospholipid and protein components of the cell membrane. NaOH denatures plasmid DNA and proteins

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6
Q

SL048

A

0.4 M NaOH, SL002 component

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7
Q

SL047

A

2% SDS, component of SL002

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8
Q

SL003

A

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

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9
Q

SL042

A

Alkaline lysis precipitation buffer. 3.84M CaCl. Helps precipitate RNA

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10
Q

SL017

A

Used during DEAE equilibration, DEAE wash 2, DEAE elution. ~1.12 M NaCl, 50mM Tris, 10mM EDTA, HCl

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11
Q

SL018

A

Used during DEAE/HLD equilibration, DEAE wash 1/2, HLD wash 1/2/elution, HLD Resin Strip

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12
Q

SL021

A

Used for HLD equilibration, loading (diluent), HLD Wash 1/2/elution. 3M ammonium sulfate 50mM Tris, 10mM EDTA

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13
Q

SL019/40

A

DEAE Resin Strip. 1M NaOH, 2M NaCl. SL040 uses liquids, SL019 uses solids

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14
Q

SL020

A

20% EtOH, DEAE monolith storage

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15
Q

0.1 M NaOH

A

HLD monolith storage

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16
Q

Lysis Buffers

A
  1. SL001
  2. SL002 = SL047 + SL048
  3. SL003
  4. SL042
17
Q

1 M NaOH

A

Chromatography Wash buffer

18
Q

SL067

A

Final Formulation Buffer. 10mM Tris, 1mM EDTA, HCL