The ANP32B antibody is a specialized immunological tool targeting acidic nuclear phosphoprotein 32 family member B (ANP32B), a conserved regulatory protein involved in cell differentiation, apoptosis, and proliferation . This antibody enables researchers to study ANP32B's roles in physiological and pathological processes, including cancer progression, immune regulation, and viral infections. ANP32B antibodies are critical for techniques such as Western blot (WB), immunohistochemistry (IHC), and immunofluorescence (IF/ICC) .
ANP32B antibodies have been instrumental in uncovering the protein's immunomodulatory functions. Studies using Anp32b knockout (KO) mice revealed:
Enhanced autoimmune responses in experimental autoimmune encephalomyelitis (EAE), with increased Th17 cell activity and proinflammatory cytokine production (e.g., IL-17A, TNF-α) .
Hyperactivation of T lymphocyte pathways and altered CD4+/CD8+ T-cell ratios, linking ANP32B deficiency to autoimmune dysregulation .
ANP32B antibodies validate its overexpression in malignancies and mechanistic roles:
Breast Cancer: ANP32B promotes tumor progression by regulating AKT phosphorylation. Silencing ANP32B reduces cell proliferation and induces G1 arrest .
Chronic Myeloid Leukemia (CML): ANP32B represses p53 activity, sustaining leukemic stem cell survival. Clinical samples show elevated ANP32B levels in CML bone marrow .
Hepatocellular Carcinoma (HCC): ANP32B knockdown reduces apoptosis by modulating Bad phosphorylation and Bak/Bax expression .
Key findings using ANP32B-targeted siRNA and antibodies include:
Diagnostic Utility: ANP32B antibodies detect overexpression in breast cancer and CML, correlating with histopathological severity .
Therapeutic Targets: ANP32B inhibition reduces viral replication (e.g., influenza, henipavirus) and sensitizes cancer cells to apoptosis .
Autoimmune Disorders: Dysregulated ANP32B expression may contribute to Th17-driven pathologies, suggesting immunotherapeutic applications .