BACE1 Specific Neutra™ Antibody Products

Beta-secretase 1 (BACE1), also known as β-secretase, is a type I transmembrane protease. BACE1 cleaves the membrane-bound APP at the N-terminus to extracellularly release the soluble APP. BACE1 is associated with Alzheimer's Disease (AD) and Myositis.

Its Gene ID: 23621, UniProtKB ID: P56817, and OMIM ID: 604252.

Defective Signaling Pathways of BACE1

To study the molecular basis of BACE1-associated pathological generation and progression of AD, we focused on the defective signaling pathways of BACE1.

• BACE1 promotes the production of insoluble Aβ isoforms.
• NF-κB activation increases BACE1 expression, Aβ production, and downstream signaling pathways.
• GSK3β triggers the activation of NF-κ, sequential BACE1 expression and Aβ production.

Fig.1 BACE1 associated defective signaling pathways.¹

Therapeutic Strategies for BACE1

BACE1 activity is a key factor for the pathogenesis of AD, which highlights the potential of BACE1 as a promising target for the diagnosis and treatment research of AD. The BACE1-related strategies are listed below:

• The concentration level and the enzymatic activity of BACE1 could be monitored as biomarkers for the treatments of AD by targeting BACE1.
• Small-molecule inhibitors of BACE1 could be developed to lower the insoluble Aβ levels.

• BACE1-based bispecific antibodies that could penetrate the blood-brain barrier may alleviate the dysfunction and progression of AD pathology. As shown in Fig.2, the transferrin-BACE1 bispecific antibody guarantees higher antibody working concentrations in the brain and enhanced therapeutic responses.

Creative Biolabs offers various anti-BACE1 antibodies for research in neuroscience and oncology. These antibodies could be used in applications such as immunoassays, blocking and neutralization. We also offer a customized service for the development of BACE1-based bispecific antibodies and monoclonal antibodies.

REFERENCE

1. Bazzari, Firas H., and Amjad H. Bazzari. "BACE1 Inhibitors for Alzheimer's Disease: The Past, Present and Any Future?." Molecules 27.24 (2022): 8823. Distributed under Open Access license CC BY 4.0, without modification.