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Human ACPP ELISA Kit für Sandwich ELISA - ABIN2683328
Kirschenbaum, Izadmehr, Yao, OConnor-Chapman, Huang, Gregoriades, Yakar, Levine: Prostatic Acid Phosphatase Alters the RANKL/OPG System and Induces Osteoblastic Prostate Cancer Bone Metastases. in Endocrinology 2016
Human ACPP ELISA Kit für Sandwich ELISA - ABIN414438
Kope?, Moertl, Steiner, St?pie?, Miko?ajczyk, Podolec, Waligóra, St?pniewski, Tomkiewicz-Paj?k, Guzik, Podolec: Markers of thrombogenesis and fibrinolysis and their relation to inflammation and endothelial activation in patients with idiopathic pulmonary arterial hypertension. in PLoS ONE 2013
Enhanced TDPase and TMPase activities may contribute to the reduction of TDP level in AD patients. The results imply that an imbalance of phosphorylation-dephosphorylation related to thiamine and glucose metabolism may be a potential target for AD prevention and therapy.
Thirteen single nucleotide polymorphism (SNPs) in acid phosphatase prostate (ACPP) were suggested as candidate causal alleles that underlie ACPP regulation and expression.
we have measured the intramolecular diffusion of the full length and 8-residue deletion peptides at two different pHs (zeige PCBD1 ELISA Kits) and found a correlation with fibrillization lag (zeige STMN1 ELISA Kits) time. These results can be explained by a simple kinetic model of the early stages of aggregation in which oligomerization is controlled by the rate of peptide reconfiguration.
Prostatic acid phosphatase delays prostate cancer cell growth in G1 phase of the cell cycle.
Studies suggest that understanding of prostatic acid phosphatase function and regulation of expression will have a significant impact on understanding prostate cancer (PCa (zeige FLVCR1 ELISA Kits)) progression and therapy.
Certain factors identified within semen, termed semen-derived enhancers of virus infection (SEVI), fragments of prostatic acid phosphatase, have been shown to significantly enhance HIV-1 infectivity.
ACPP increases significantly in epithelial cells of ovarian carcinoma, which indicates that it may be a candidate biomarker for diagnosis of epithelia-derived ovarian cancer in women.
Data indicate that hypoxia regulates prostatic acid phosphatase (PAP) through hypoxia-inducible factor 2 alpha (zeige EPAS1 ELISA Kits) (HIF2alpha (zeige EPAS1 ELISA Kits)) and from stimulated A2B (zeige ADORA2B ELISA Kits) adenosine receptors.
GCNT1 (zeige GCNT1 ELISA Kits) is over-expressed in prostate cancer and is associated with higher levels of core 2 O-sLe(x) in PSA (zeige PLAG1 ELISA Kits), PAP (zeige REG3A ELISA Kits) and MUC1 (zeige MUC1 ELISA Kits) proteins.
Data indicate that prostate acid phosphatase-based peptide vaccine PAP (zeige REG3A ELISA Kits)-114-128 peptide appears to be a relevant for the treatment of prostate cancer.
PAP (zeige ASAP1 ELISA Kits)-immunoreactivity was present in type I and one of type III taste cells of taste buds. Thus, it is suggested that PAP (zeige ASAP1 ELISA Kits) might be a responsible ectoenzyme for metabolism of extracellular nucleotides, being involved in the regulation of taste signaling in taste buds.
These findings demonstrate that PAP (zeige ASAP1 ELISA Kits) secreted by PCa (zeige ENPP1 ELISA Kits) cells in OB bone metastases increases osteoprotegerin (zeige TNFRSF11B ELISA Kits) and plays a critical role in the vicious cross talk between cancer and bone cells.
functional PAP (zeige ASAP1 ELISA Kits)(thorn) neurons are essential for the analgesic effect, which is mediated by NGF (zeige NGFB ELISA Kits)-trkA (zeige NTRK1 ELISA Kits) signaling.
TMPAP is involved in the control of GABAergic tone in the brain also through exocytosis, and that PAP (zeige ASAP1 ELISA Kits) deficiency produces a distinct neurological phenotype.
In male mouse saliva (zeige RAG1AP1 ELISA Kits) prostatic acid phosphatase regulates salivation.
Data indicate that prostate acid phosphatase-based peptide vaccine PAP (zeige ASAP1 ELISA Kits)-114-128 peptide appears to be a relevant for the treatment of prostate cancer.
this PAP (zeige ASAP1 ELISA Kits)-/- mouse model shows that TMPAP is required for the normal function of prostate in mice, and its deficiency leads to prostate adenocarcinoma.
Both prostatic acid phosphatase and ecto-5'-nucleotidase generate adenosine in the dorsal spinal cord.
Prostatic acid phosphatase is required for the antinociceptive effects of thiamine and benfotiamine.
Experiments indicate that PAP (zeige ASAP1 ELISA Kits) and NT5E (zeige NT5E ELISA Kits) are the main ectonucleotidases that generate adenosine in nociceptive circuits and indicate these enzymes transform pulsatile or sustained nucleotide release into an inhibitory adenosinergic signal.
The obtained N-terminal amino-acid sequence of boar PTAP showed 92% identity with the N-terminal amino-acid sequence of human PAP (zeige PDAP1 ELISA Kits). The determined sequence of a 354 bp nucleotide fragment showed 90% identity with the corresponding sequence of human PAP (zeige PDAP1 ELISA Kits).
This gene encodes an enzyme that catalyzes the conversion of orthophosphoric monoester to alcohol and orthophosphate. It is synthesized under androgen regulation and is secreted by the epithelial cells of the prostate gland. An alternatively spliced transcript variant encoding a longer isoform has been found for this gene. This isoform contains a transmembrane domain and is localized in the plasma membrane-endosomal-lysosomal pathway.
, prostatic acid phosphatase
, prostatic acid phosphotase
, thiamine monophosphatase
, fluoride-resistant acid phosphatase
, lysosomal acid phosphatase
, prostatic acid phosphatase (rPAP)
, acid phosphatase, prostate
, tyrosine acid phosphatase
, prostatic acid phosphatase-like
, testicular acid phosphatase homolog