NSE Rabbit polyclonal Antibody IgG
Fig1: Western blot analysis on different cell lysates using anti-NSE rabbit polyclonal antibodies.
Fig2: ICC staining NSE in Hela cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig3: Western blot analysis of NSE on hybrid fish (crucian-carp) brain tissue lysate using anti-NSE antibody at 1/500 dilution.
Host Species; Species ReactivityRabbit; Human, Mouse, Rat, Zebrafish
Application SummaryWB, ICC
Purification; FormulationPeptide affinity purified; 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.; Liquid form.
ALTnamesGamma-enolase,2-phospho-D-glyceRate hydro-lyase，Enolase 2，Neural enolase，Neuron-specific enolase
BackgroundGamma-enolase is one of the three enolase isoenzymes found in mammals. This isoenzyme, a homodimer, is found in mature neurons and cells of neuronal origin. A switch from alpha enolase to gamma enolase occurs in neural tissue during development in rats and primates. Detection of NSE with antibodies can be used to identify neuronal cells and cells with neuroendocrine differentiation. NSE is produced by small cell carcinomas which are neuroendocrine in origin. NSE is therefore a useful tumor marker for lung cancer patients.(R1401-6)