The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders.
Purified antibody in PBS with 0.05% sodium azide
4℃; -20℃ for long term storage
Figure 1:Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Figure 2:Western blot analysis using CPT2 mAb against human CPT2 (AA: 26-178) recombinant protein. (Expected MW is 21.4 kDa)
Figure 3:Western blot analysis using CPT2 mAb against HEK293-6e (1) and CPT2 (AA:26-178)-hIgGFc transfected HEK293-6e (2) cell lysate.
Figure 4:Western blot analysis using CPT2 mouse mAb against MCF-7 (1), Hela (2), NIH/3T3 (3) and PC-12 (4) cell lysate.
Figure 5:Flow cytometric analysis of Hela cells using CPT2 mouse mAb (green) and negative control (red).
For Research Use Only. Not for use in diagnostic procedures.