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Recombinant full length protein corresponding to Human BDNF (N terminal). (Purified from E.coli).
Database link: P23560
For BDNF, multiple WB bands are possible and expected. The human protein has 5 isoforms (precursors: 28 – 37 kDa) and can be glycosylated (Uniprot: http://www.uniprot.org/uniprot/P23560). The mature form is expected at ~14 kDa (monomer) and the dimer at ~28 kDa.
Our Abpromise guarantee covers the use of ab205067 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||Use a concentration of 0.2 - 2 µg/ml. Predicted molecular weight: 15 kDa.|
|ICC/IF||Use a concentration of 0.33 - 20 µg/ml.|
|IHC-P||Use a concentration of 5 µg/ml. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.|
This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel ran at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for 1 hour before incubation with ab205067 (2.5 microgram /mL) overnight at 4°C. Antibody binding was detected using infrared labelled goat anti-mouse IgG (green) at a 1:10,000 dilution for 1 hour at room temperature.
Immunofluorescent analysis of U2OS cells labeling BDNF with ab205067 at 0.33 µg/ml, followed by Goat anti-mouse AlexaFluor488 secondary antibody. For nuclear staining DAPI was used. A: proBDNF-expressing U2OS cells; B. Negative control (non-transfected U2OS cells).
Immunohistochemical analysis of formalin-fixed, paraffin-embedded Human cerebral cortex tissue sections from Alzheimer's disease patients labeling BDNF with ab205067 at 5 µg/ml, followed by peroxidase secondary detection and DAB staining. A: BDNF staining by ab205067; B.Negative staining without primary antibody. Sections were counterstained with toluidine blue.