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Synthetic peptide, corresponding to 20 residues from the C-terminus of rat EAAT1 (Peptide available as ab127026.)
Our Abpromise guarantee covers the use of ab416 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|IHC-FoFr||Use at an assay dependent concentration. PubMed: 18714338|
|WB||1/200 - 1/5000. Predicted molecular weight: 60 kDa.Can be blocked with EAAT1 peptide (ab127026).|
|ICC||Use at an assay dependent concentration.|
|Flow Cyt||1/10 - 1/200.|
|IHC-P||1/50 - 1/500.|
|ICC/IF||Use at an assay dependent concentration.|
ab416 staining zebrafish retina sections by IHC-Fr. The tissue was fixed with paraformaldehyde and an antigen retrieval step was performed with sodium citrate pH 6. Blocking of the sample was done with 5%BSA in PBS containing 01% Tween 20 and 0.5% Triton X, for 60 minutes at 23°C, followed by staining with ab416 at 1/100 in blocking solution for 16h at 4°C. An alexa 488 conjugated goat anti-rabbit polyclonal antibody at 1/1000 was used as the secondary antibody. Nuclei are stained in blue with DAPI. EAAT1 expression can be observed in the inner plexiform layer (in green).
ab416 staining EAAT1 in Chicken retina cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with paraformaldehyde, permeabilized with Triton X-100 0.02% in PBS and blocked with 5% serum for 16 hours at 22°C. Samples were incubated with primary antibody (1/500 in PBS + 0.02% Triton) for 16 hours at 22°C. An undiluted Alexa Fluor®488-conjugated Goat anti-rabbit IgG polyclonal was used as the secondary antibody.