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ACP2 encodes the beta subunit of lysosomal acid phosphatase (LAP). Additionally we are shipping ACP2 Kits (16) and ACP2 Proteins (8) and many more products for this protein.
Showing 10 out of 32 products:
Cow (Bovine) Polyclonal ACP2 Primary Antibody for WB - ABIN610822
Ireton, Davis, van Hengel, Mariner, Barnes, Thoreson, Anastasiadis, Matrisian, Bundy, Sealy, Gilbert, van Roy, Reynolds: A novel role for p120 catenin in E-cadherin function. in The Journal of cell biology 2002
Data show that lysosomal acid phosphatase 2 (ACP2) was overexpressed in colorectal cancer (CRC (show CALR Antibodies)) and associated with poor outcome in stage II CRC (show CALR Antibodies), 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 (show CALR Antibodies) patients receiving chemotherapy.
An enzymatically inactive allel (show SCN7A Antibodies)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 Antibodies) and is needed for hydrolysis and removal of degradation products
Acp2 is the gene mutated in nax (show SCN7A Antibodies) 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 Antibodies) 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