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Invitrogen
Human Cathepsin D quantitates human Cathepsin D in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human Cathepsin D.
Cathepsin D is a gene located on chromosome 11p15.5 that encodes a lysosomal aspartic protease involved in the degradation of proteins. This enzyme is widely expressed in various tissues but is particularly abundant in the liver, kidneys, and brain, where it plays a crucial role in intracellular protein catabolism and turnover. Cathepsin D is synthesized as an inactive precursor, procathepsin D, which is activated in the acidic environment of lysosomes. Beyond its fundamental role in protein degradation, Cathepsin D has been implicated in several physiological and pathological processes, including apoptosis, hormone processing, and antigen presentation. Dysregulation of Cathepsin D expression or activity is associated with various diseases, such as neurodegenerative disorders, cancer, and cardiovascular diseases. In the context of cancer, Cathepsin D overexpression has been linked to tumor progression and metastasis, making it a potential biomarker and therapeutic target. Research continues to explore its diverse biological functions and therapeutic implications in various medical conditions.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Gene aliases : CLN10, CPSD, CTSD, HEL-S-130P
Gene ID : (Human) 1509
Gene symbol : CTSD
Protein Aliases : Cathepsin D, CathepsinD, Ceroid lipofuscinosis neuronal 10, MGC2311, OTTHUMP00000196039, OTTHUMP00000198692, ceroid-lipofuscinosis, neuronal 10, epididymis secretory sperm binding protein Li 130P, lysosomal aspartyl peptidase, lysosomal aspartyl protease
UniProt ID (Human) P07339
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