The UMODL1 Polyclonal Antibody (PACO59932) is a valuable tool for researchers studying UMODL1, a protein involved in various cellular processes, including immune regulation and inflammation. This antibody, generated in rabbits, exhibits high reactivity with human samples and has been validated for use in Western blot applications. By binding to the UMODL1 protein, this antibody enables detection and analysis in a range of cell types, making it a versatile option for studies in immunology, inflammation, and disease research.UMODL1, also known as UMODL1 protein, is a key player in the immune system, helping to regulate immune responses and maintain immune homeostasis.
Its involvement in inflammatory pathways and disease development underscores its importance as a target for investigations into conditions such as autoimmune disorders, inflammation-related diseases, and cancer. By elucidating the function of UMODL1, researchers can uncover new insights into disease mechanisms and potentially identify novel therapeutic strategies for immune-related disorders.
Western Blot. Positive WB detected in: NIH/3T3 whole cell lysate, MCF-7 whole cell lysate. All lanes: UMODL1 antibody at 5.1µg/ml. Secondary. Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 145, 157, 137, 150 kDa. Observed band size: 145, 157 kDa.
IHC image of PACO59932 diluted at 1:300 and staining in paraffin-embedded human prostate cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
IHC image of PACO59932 diluted at 1:300 and staining in paraffin-embedded human colon cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
