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ACP2 encodes the beta subunit of lysosomal acid phosphatase (LAP). Zusätzlich bieten wir Ihnen ACP2 Antikörper (36) und ACP2 Proteine (12) und viele weitere Produktgruppen zu diesem Protein an.
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In addition to replicating a previously identified genome-wide significant locus for corneal astigmatism near the PDGFRA gene, gene-based analysis identified three novel candidate genes, CLDN7, ACP2, and TNFAIP8L3, that warrant further investigation to understand their role in the pathogenesis of corneal astigmatism. (Meta-analysis)
Data show that lysosomal acid phosphatase 2 (ACP2) was overexpressed in colorectal cancer (CRC (zeige CALR ELISA Kits)) and associated with poor outcome in stage II CRC (zeige CALR ELISA Kits), and that high expression of ACP2 patients were more sensitive to chemotherapy than those with a low expression, suggesting ACP2 as a marker for CRC (zeige CALR ELISA Kits) patients receiving chemotherapy.
An enzymatically inactive allel (zeige SCN7A ELISA Kits)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 (zeige ACP5 ELISA Kits) and is needed for hydrolysis and removal of degradation products
Acp2 is the gene mutated in nax (zeige SCN7A ELISA Kits) 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 (zeige LAMP2 ELISA Kits) 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