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Human Prosaposin ELISA Kit für Sandwich ELISA - ABIN366591
Ali, Creevey, Hao, McCartan, OGaora, Hill, Young, McIlroy: Prosaposin activates the androgen receptor and potentiates resistance to endocrine treatment in breast cancer. in Breast cancer research : BCR 2015
Data show that matrix (ECM (zeige MMRN1 ELISA Kits)) stiffness leads to mechano-signal transduction in mesenchymal stem cells (MSC (zeige MSC ELISA Kits)), which promotes mammary tumor growth in part through secretion of the signaling protein prosaposin.
Data suggested that the abundance of Psap in sperm sample may be a sensitive endpoint to predict PCB (zeige PC ELISA Kits) exposure.
Prosaposin facilitates sortilin (zeige SORT1 ELISA Kits)-independent lysosomal trafficking of progranulin (zeige GRN ELISA Kits).
Mesotrypsin (zeige PRSS3 ELISA Kits) generated saposins A-D from prosaposin, and mature caspase-14 (zeige CASP14 ELISA Kits) contributed to this process by activating mesotrypsinogen (zeige PRSS3 ELISA Kits) to mesotrypsin (zeige PRSS3 ELISA Kits). Knockdown of these proteases markedly down-regulated saposin A synthesis in skin equivalent models.
Low levels of prosaposin and its receptors in the mouse brain suggest the participation of prosaponin in pathological changes in the brains of dystrophic mdx (zeige DMD ELISA Kits) mice.
These data show functional association between GPR37, prosaposin, and GM1 ganglioside in the plasma membrane.
Prosaposin is involved in the regulation of muscle differentiation of regenerated fibres
Saposins A and B deficiencies attenuated GalCer-beta-galactosylceramidase (zeige GALC ELISA Kits) and GM1-beta-galactosidase (zeige GLB1 ELISA Kits) functions in the degradation of lactosylceramide in the liver.
These data suggest that prosaposin plays an important role in the neuronal maturation processes of the vestibular sensory epithelium and the maintenance of normal vestibular system function.
The saposin C deficient mice backcrossed to point mutated GCase (zeige GBA ELISA Kits) mimics the central nervous system phenotype and biochemistry of some type 3 (neuronopathic) variants of Gaucher disease.
This report documents the successful use of plasma lysoSLs profiling in the PSAP deficiency diagnosis, as a reliable and informative tool to obtain a preliminary information in infantile cases with complex traits displaying severe neurological signs and visceral involvement.
an extensive review of all the PSAP-causative variants published in the literature to date, accounting for a total of 10 PSAP allele types (review)
Our findings suggest a novel pharmacological approach to Sap (zeige APCS ELISA Kits) C deficiency directed to treat major secondary pathological aspects in this disorder.
PSAP is a secreted biomarker.
findings support a lung metastasis-promoting function of the miR (zeige MLXIP ELISA Kits)-23b/27b/24 cluster of miRNAs, which functions in part through the direct inhibition of PSAP in breast cancer
Of the 2575 proteins identified, proteins upregulated in gallbladder cancer included several lysosomal proteins such as prosaposin, cathepsin Z (zeige CTSZ ELISA Kits) and cathepsin H (zeige CTSH ELISA Kits).
Saposin C protects glucocerebrosidase against alpha-synuclein inhibition.
identified 68 single-nucleotide polymorphisms and 9 indels in the pig PASP (zeige CPB1 ELISA Kits) gene, and three single-nucleotide polymorphisms were nonsynonymous substitutions
Saposin B (Sap (zeige APCS ELISA Kits) B) is not a limiting factor of the coupled Sap (zeige APCS ELISA Kits) B-arylsulfatase A (zeige ARSA ELISA Kits) reaction in mouse kidney cells even if sulfatide has accumulated to unphysiologically high levels.
This gene encodes a highly conserved glycoprotein which is a precursor for 4 cleavage products: saposins A, B, C, and D. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities. Mutations in this gene have been associated with Gaucher disease, Tay-Sachs disease, and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants encoding different isoforms.
prosaposin (variant Gaucher disease and variant metachromatic leukodystrophy)
, proactivator polypeptide-like
, mitochondrial carrier homolog 1
, mitochondrial carrier-like protein 1
, proactivator polypeptide
, sphingolipid activator protein-1
, snoRNA MBII-198
, sulfated glycoprotein 1
, prosaposin (sulfated glycoprotein, sphingolipid hydrolase activator)
, Surfactant-associated protein 1 (pulmonary surfactant protein SP-A)
, Surfactant-associated protein 1 (pulmonary surfactant protein, SP-A)
, pulmonary surfactant-associated protein A
, surfactant associated protein A
, surfactant, pulmonary-associated protein A1