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anti-Mouse (Murine) Prosaposin Antikörper:
anti-Human Prosaposin Antikörper:
anti-Rat (Rattus) Prosaposin Antikörper:
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Human Monoclonal Prosaposin Primary Antibody für ICC, FACS - ABIN1098150
Xu, Deng, Mao, Zhang, Wang, Wang, Mu, Deng, Ma: The interaction of the second Kunitz-type domain (KD2) of TFPI-2 with a novel interaction partner, prosaposin, mediates the inhibition of the invasion and migration of human fibrosarcoma cells. in The Biochemical journal 2011
Show all 2 Pubmed References
Human Monoclonal Prosaposin Primary Antibody für IHC (p), IP - ABIN562465
Koochekpour, Hu, Vellasco-Gonzalez, Bernardo, Azabdaftari, Zhu, Zhau, Chung, Vessella: Serum prosaposin levels are increased in patients with advanced prostate cancer. in The Prostate 2012
Data suggested that the abundance of Psap in sperm sample may be a sensitive endpoint to predict PCB (zeige PC Antikörper) exposure.
Prosaposin facilitates sortilin (zeige SORT1 Antikörper)-independent lysosomal trafficking of progranulin (zeige GRN Antikörper).
Mesotrypsin (zeige PRSS3 Antikörper) generated saposins A-D from prosaposin, and mature caspase-14 (zeige CASP14 Antikörper) contributed to this process by activating mesotrypsinogen (zeige PRSS3 Antikörper) to mesotrypsin (zeige PRSS3 Antikörper). 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 Antikörper) 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 Antikörper) and GM1-beta-galactosidase (zeige GLB1 Antikörper) 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 Antikörper) mimics the central nervous system phenotype and biochemistry of some type 3 (neuronopathic) variants of Gaucher disease.
UGT1 aids in the folding of sequential domain-containing proteins such as prosaposin.
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 Antikörper) 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 Antikörper)-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 Antikörper) and cathepsin H (zeige CTSH Antikörper).
Saposin C protects glucocerebrosidase against alpha-synuclein inhibition.
identified 68 single-nucleotide polymorphisms and 9 indels in the pig PASP (zeige CPB1 Antikörper) gene, and three single-nucleotide polymorphisms were nonsynonymous substitutions
Saposin B (Sap (zeige APCS Antikörper) B) is not a limiting factor of the coupled Sap (zeige APCS Antikörper) B-arylsulfatase A (zeige ARSA Antikörper) 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