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ACP2 encodes the beta subunit of lysosomal acid phosphatase (LAP). Additionally we are shipping ACP2 Antibodies (32) and ACP2 Kits (8) and many more products for this protein.
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An enzymatically inactive allel (show SCN7A Proteins)e of mouse Acp2 causes cerebellum abnormalities, growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype.
ACP2 has critical roles in the development of the anterior cerebellum and it may regulate anterior and central zone compartmentation.
These data suggest that ACP2 expression is dynamically regulated during development, and in the adult, it may function within a complex architecture that is linked to cerebellar modular organization.
dephosphorylation of Man6P-containing lysosomal proteins requires the concerted action of Acp2 and Acp5 (show ACP5 Proteins) and is needed for hydrolysis and removal of degradation products
Acp2 is the gene mutated in nax (show SCN7A Proteins) mice provides a valuable model system for studying the role of Acp2 in cerebellum and skin homeostasis.
The data suggest that lysosomal dysfunction and accumulation of storage material require increased biogenesis of LAP/ACP2 and LAMP-2 (show LAMP2 Proteins) positive membranes which makes LAP/ACP2 suitable as biomarker of Batten disease.
This gene encodes the beta subunit of lysosomal acid phosphatase (LAP). LAP is chemically and genetically distinct from red cell acid phosphatase. The encoded protein belongs to a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Mutations in this gene or in the related alpha subunit gene cause acid phosphatase deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
lysosomal acid phosphatase
, lysosomal acid phosphatase 2
, acid phosphatase 2, lysosomal
, Acid phosphatase 2, lysozymal
, LMW-PTP-II low molecular weight phosphotyrosine protein phosphatase isozyme 2