The CXorf36 Polyclonal Antibody (PAC060416) is a valuable tool for researchers studying the CXorf36 protein, a little-known gene with potential implications in various biological processes. Raised in rabbits, this antibody is highly specific to human samples and has been validated for use in Western blot applications. By targeting the CXorf36 protein, this antibody allows for the detection and analysis of this protein in different cell types, making it a versatile tool for studies in various areas of biology and disease research.
Although the exact function of CXorf36 is still being elucidated, preliminary research suggests its involvement in cellular processes and potential associations with certain diseases. By understanding the role of CXorf36, researchers can gain insights into its function in different cellular pathways, providing potential new targets for therapeutic interventions. This antibody is an essential tool for those interested in exploring the functions and implications of CXorf36 in different biological contexts.
Western Blot. Positive WB detected in: HepG2 whole cell lysate, SH-SY5Y whole cell lysate, PC-3 whole cell lysate. All lanes: CXorf36 antibody at 3.9µg/ml. Secondary. Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 49, 21 kDa. Observed band size: 49 kDa.
IHC image of PACO60416 diluted at 1:400 and staining in paraffin-embedded human endometrial 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 PACO60416 diluted at 1:400 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.
Background:
regulation of signal transduction
Synonyms:
Deleted in autism-related protein 1, CXorf36, DIA1R
