Lipoprotein Lipase Antibody / Fatty Acid Mobilization Protein Antibody (F43589)

Lipoprotein Lipase Antibody Human Brain IHC. Immunohistochemical staining of formalin-fixed, paraffin-embedded human brain tissue using Lipoprotein Lipase Antibody demonstrates cytoplasmic HRP-DAB brown staining within scattered neural cell populations against a background of neuropil-rich tissue architecture. The staining pattern is consistent with expression of Lipoprotein Lipase (LPL), a key enzyme involved in triglyceride hydrolysis, fatty acid mobilization, and lipid utilization. LPL contributes to lipid processing pathways that support cellular energy balance and membrane maintenance, processes that are particularly important in metabolically active tissues. The observed staining supports the role of LPL in regulating lipid availability and fatty acid utilization within the central nervous system.

Lipoprotein Lipase Antibody HL-60 Western Blot. Western blot analysis of HL-60 cell lysate using Lipoprotein Lipase Antibody demonstrates a distinct band at approximately 55 kDa, consistent with expression of Lipoprotein Lipase (LPL). LPL is a key enzyme involved in triglyceride hydrolysis, fatty acid mobilization, and lipid utilization, facilitating the release of free fatty acids from circulating lipoproteins for cellular uptake and metabolic activity. Detection of LPL in HL-60 cells supports its role in pathways governing lipid handling, energy metabolism, and cellular nutrient utilization. The observed signal at the expected molecular weight provides validation of target recognition by the antibody.

Lipoprotein Lipase Antibody HeLa Cell FACS. Flow cytometric analysis of HeLa cells using Lipoprotein Lipase Antibody demonstrates a pronounced rightward shift of the positive cell population (green) relative to the negative control (blue), consistent with expression of Lipoprotein Lipase (LPL). LPL is a key enzyme involved in triglyceride hydrolysis, fatty acid mobilization, and lipid utilization, facilitating the release of free fatty acids from circulating lipoproteins for cellular uptake and metabolic activity. Detection of LPL by flow cytometry supports its role in cellular lipid handling and nutrient utilization pathways. FITC-conjugated goat anti-rabbit secondary antibody was used for signal detection.