Antibodies |
For any antibody (including secondary antibodies) used, the Methods section should include the following: |
Methods |
1a |
The commercial (or other) source. |
Methods |
1b |
The species in which the antibody was raised, catalogue and batch/lot numbers. |
Methods |
1c |
The epitope against which it was raised. |
Methods |
1d |
The isotype (IgG, IgM, IgY, etc) and clone numbers (if applicable). |
Methods |
1e |
When available, https://scicrunch.org/resources. |
Methods |
1f |
The diluting buffer, the final antibody dilution and number of times solutions have been re‐used. |
Methods |
Controls |
2 |
Positive and negative controls should be used, as much as possible. |
Results |
Images for review |
3 |
Full uncropped images should be made available to reviewers and editors. |
Results |
Presentation |
4 |
Separate immunoblots should NEVER be merged in figures. |
Results |
Normalisation |
5 |
For Western blotting normalisation to the loading control should be done only if the bands for the target protein and the loading control are obtained from the same blot. |
Results |
Quantitation |
6 |
Quantitation of band density can only be conducted on analysis within the linear range. |
Results |
Statistical comparisons |
7 |
Statistical comparisons should only be carried out between bands on the same blot. |
Results |
Blinding |
8 |
Full details of blinding for analysis of images should be provided. |
Methods |