DNA purification buffers, mostly copied from OpenWetware and Genesee by Shyam Bhakta. <Email for suggestions. Qiagen.com buffers.
Do not autoclave solutions containing ethanol, isopropanol or MOPS; use filter-sterilization if necessary with compatible filter type (nylon for alcohol solns; PES otherwise).
Adjust pH of Tris (base) solutions with HCl.
- Buffer P1 — miniprep resuspension buffer, store 4°C after RNase addition, cat#19051
- 50 mM Tris-HCl, pH 8.0
- 10 mM EDTA
- 100 mg/L RNase A
- 100 mg/mL (1000×) RNase A can be purchased: Qiagen 19101
- Buffer P2 — miniprep lysis buffer, cat#19052
- 200 mM NaOH
- 1%m/V, 10 g/L SDS
- 43 mg/L thymophthalein in ethanol (opt)
- Buffer N3 — miniprep neutralization buffer, cat#19064
- 4.2 M Gu-HCl, guanidinium chloride
- 0.9 M KOAc
- HCl → pH 4.8
- Buffer PB — DNA-column binding buffer, miniprep opt wash buffer, cat#19066
- 5 M Gu-HCl
- 30%V/V isopropanol (300 mL/L)
- Buffer PE — miniprep final wash buffer, cat#19065
- 10 mM Tris-HCl, pH 7.5
5× PE base: 50 mM Tris-HCl pH 7.6
50× PE base: 0.5 M Tris-HCl pH 7.8 (use 20 mL/L + 180 mL/L water) - 80%V/V ethanol (800 mL/L)
- 10 mM Tris-HCl, pH 7.5
- Buffer EB — miniprep elution buffer
- 10 mM Tris-HCl, pH 8.5
- Buffer AE — genomic DNA elution buffer
- 10 mM Tris-HCl, pH 9.0
- 0.5 mM EDTA
- Buffer QG — gel solubilization and column binding buffer, cat#19063
- 5.5 M GuSCN, guanidinium thiocyanate
- 20 mM Tris-HCl, pH 6.6
- Buffer QX1 — gel solubilization and column binding buffer, cat#20912
7 M NaPO₄ <insoluble- 7 M NaClO₄
- 10 mM NaOAc, pH 5.3
- Buffer P3 — QIAfilter/tip DNA prep neutralization buffer
- 3.0 M KOAc, pH 5.5
adjust pH with glacial acetic acid, ≈110 mL/L.
- 3.0 M KOAc, pH 5.5
- Buffer DP3 — Qiagen Directprep 96-well miniprep
- 3.0 M NH₄OAc, pH 5.5
- Buffer QXB — for binding >3 kb fragments to columns, cat#19054
- 5 M Gu-HCl
- Buffer FWB2 — QIAfilter wash buffer
- 1 M KOAc, pH 5.0
- Buffer QBT — QIAfilter equilibration buffer
- 750 mM NaCl
- 50 mM MOPS, pH 7.0
- 15% isopropanol (150 mL/L)
- 0.15%, 1.5 g/L Triton X-100
- Buffer QC — QIAfilter/tip wash buffer, cat#19055
- 1.0 M NaCl
- 50 mM MOPS pH 7.0
- 15% isopropanol (150 mL/L)
- Buffer QF — QIAfilter elution buffer, cat#19056
- 1.25 M NaCl
- 50 mM Tris-HCl, pH 8.5
- 15% isopropanol (150 mL/L)
- Buffer QN — EndoFree QIAfilter elution buffer
- 1.6 M NaCl
- 50 mM MOPS, pH 7.0
- 15% isopropanol (150 mL/L)
- Buffer B1 — bacterial lysis buffer
- 50 mM Tris-HCl, pH 8.0
- 50 mM EDTA
- 0.5%, 5 g/L Tween-20
- 0.5%, 5 g/L Triton X-100
- 200 μg/L RNase A
- Buffer B2 — bacterial lysis buffer
- 3 M Gu-HCl
- 20%, 200 g/L Tween-20
- Buffer C1 — cell lysis buffer, store 4°C
- 1.28 M sucrose
- 40 mM Tris-HCl, pH 7.5
- 20 mM MgCl₂
- 4%, 40 g/L Triton X-100
- Buffer G2 — digestion buffer
- 800 mM Gu-HCl
- 30 mM Tris-HCl, pH 8.0
- 30 mM EDTA
- 5%, 50 g/L Tween-20
- 5%, 50 g/L Triton-X100
- Buffer Y1 — yeast lysis buffer, store 4̈°C
- 1 M sorbitol
- 100 mM EDTA pH 8.0
- 14 mM β-mercaptoethanol (added just before use)
- Buffer PAA — PAGE DNA elution
- 500 mM NH₄OAc
- 100 mM Mg(OAc)₂
- 1 mM EDTA
- 0.1% SDS
- Buffer TE — DNA elution/resuspension/storage buffer
- 10 mM Tris-HCl, pH 8.0
- 0.1 or 1 mM EDTA
- Buffer STE — DNA resuspension/storage buffer
- 100 mM NaCl
- 10 mM Tris-HCl, pH 8.0
- 1 mM EDTA
- LyseBlue®, 1000× — pH indicator, clear→blue ≥pH 9.3
- 43 mg/mL thymophthalein
- in ethanol
- Buffer P1 base, 1 L:
- 6.06 g Tris base
- 2.922 g EDTA
- 12 M HCl → pH 8.0, ≈300–400 µL
- Add 50 µL RNase A to each new 50 mL aliquot, stored 4°C.
- Buffer P2, 1 L:
- 8 g NaOH
- 10 g SDS
- Buffer N3, 1 L:
- 401.2 g Gu-HCl, guanidinium chloride
- 88.33 g KOAc, potassium acetate
- 12 M HCl → pH 4.8, ≈32 mL
- Buffer PE 50× base (0.5 M Tris-Cl), 0.25 L:
- 15.14 Tris base
- 12 M HCl → pH 7.8
- → 250 mL
- Buffer PE, 1 L:
- 20 mL 50× PE base
- 180 mL Milli-Q water
- 800 mL Ethanol (pure), → 1 L