Apr 02, 2025

Public workspaceEB buffer V.2

  • 1Max Planck Institute for Evolutionary Anthropology
  • MPI EVA Ancient DNA Core Unit
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Document CitationAnna Schmidt, Anya Patova 2025. EB buffer. protocols.io https://dx.doi.org/10.17504/protocols.io.bp2l62rzdgqe/v2Version created by Ancient DNA Core Unit
License: This is an open access document distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Created: July 25, 2024
Last Modified: April 02, 2025
Document Integer ID: 125963
Keywords: capture, bait dilution
Funders Acknowledgements:
Max Planck Society
Grant ID: -
Abstract
EB buffer ('Elution buffer', 10 mM Tris-HCl, pH 8.0) is used in various steps of sample preparation by the Ancient DNA Core Unit of the MPI-EVA.

Changes from v1
  • Added the table with reagent details in the protocols section (Step 1). This was accidentally removed from version 1 before publishing.
Note

This protocol describes the preparation of 500 ml EB buffer.

Materials
Reagent/consumableSupplierCatalogue number
Reagents
Water Sigma Aldrich/Merck1153332500
1 M Tris-HCl, pH 8.0AppliChem A4577,1000
Consumables
5 ml serological pipetCorning BV357543
50 ml serological pipetCorning BV357550
Square media bottle 500 mlVWR391-0630

Equipment

  • Automated pipetting aid for glas pipette


Protocol

1. Prepare the buffer in a 500 ml square media bottle by adding the following reagents. Use the glass pipette for transfer of large volumes (> 1 ml). Mix reagents by shaking the bottle.

ReagentVolumeFinal concentration in reaction
Water495 ml
1 M Tris-HCl, pH 8.05 ml10 mM
sum 500 ml

Note
[Labeling]
Label the bottle with the buffer name, batch ID, date and the initials of the person who prepared the buffer.
Attention: Every single bottle prepared at the same day gets a new batch ID. Name the batches with Roman numerals (e.g. batch I, batch II, etc.)

Note
[Note]
It is also acceptable to use the scale of the bottle to fill up to ~400 ml with water, then adding the remaining 95 ml using the glass pipette.

2. Review the protocol in which the buffer is used to determine whether the buffer should be decontaminated using UV treatment. Instructions for using UV decontamination are provided in the Appendix.

Note
[Labeling]
Label the bottle with the buffer name, batch ID, date and the initials of the person who prepared the buffer.
Attention: Every single bottle prepared at the same day gets a new batch ID. Name the batches with Roman numerals (e.g. batch I, batch II, etc.)

3. Store the buffer at room temperature until used. Shelf life is at least one year from preparation.

Note
[Documentation]

Note the lot numbers, date and initials written on the reagents used for buffer preparation in Labfolder (orange fields).

Appendix

Document
UV decontamination of materials
NAME
UV decontamination of materials
CREATED BY
Elena Essel

Document
UV decontamination of reagents/buffers
NAME
UV decontamination of reagents/buffers
CREATED BY
Elena Essel