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There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). Additionally we are shipping ALP Antibodies (416) and ALP Proteins (14) and many more products for this protein.
Showing 10 out of 42 products:
Human ALP ELISA Kit for Sandwich ELISA - ABIN417005
Gassling, Hedderich, Açil, Purcz, Wiltfang, Douglas: Comparison of platelet rich fibrin and collagen as osteoblast-seeded scaffolds for bone tissue engineering applications. in Clinical oral implants research 2013
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Rat (Rattus) ALP ELISA Kit for Sandwich ELISA - ABIN431479
Gradosova, Zivna, Svejkovska, Palicka, Tichy, Zivny: The role of atorvastatin in bone metabolism in male albino Wistar rats. in Die Pharmazie 2011
Show all 6 Pubmed References
Human ALP ELISA Kit for Sandwich ELISA - ABIN456166
Partanen, Vähäkangas, Woo, Auriola, Veid, Chen, Myllynen, El Nezami: Transplacental transfer of melamine. in Placenta 2012
Mouse (Murine) ALP ELISA Kit for Sandwich ELISA - ABIN415482
Wu, Ou, Wang, Yang, Wang, Liu, Xiong, Sun, Zhang, Zhu: Icaritin induces MC3T3-E1 subclone14 cell differentiation through estrogen receptor-mediated ERK1/2 and p38 signaling activation. in Biomedicine & pharmacotherapy 2017
This meta-analysis suggests that high serum ALP level is obviously associated with lower OS rate in patients with osteosarcoma, and it is an effective biomarker of prognosis.
ASRGL1 (show ASRGL1 ELISA Kits) was closely associated with growth and apoptosis in cervical cancer. Therefore, ASRGL1 (show ASRGL1 ELISA Kits) may be a novel, potentially effective anticervical cancer therapy.
A panel including p53 (show TP53 ELISA Kits) and ASRGL1 (show ASRGL1 ELISA Kits) immunohistochemistry was identified as the most accurate predictor of relapse-free and disease-specific survival. Within this panel, patients were allocated into high- (5.9%), intermediate- (29.5%) and low- (64.6%) risk groups where high-risk patients had a 30-fold risk (P<0.001) of dying of EEC compared to the low-risk group.
In a prospective setting ASRGL1 (show ASRGL1 ELISA Kits) validates as a strong prognostic biomarker in endometrial carcinoma. Loss of ASRGL1 (show ASRGL1 ELISA Kits) is associated with aggressive disease and poor survival.
Our studies suggest that the p.G178R mutation in ASRGL1 (show ASRGL1 ELISA Kits) leads to photoreceptor degeneration resulting in progressive vision loss.
Concentrations of PLAP were elevated in gingival crevicular fluid of patients with pre-eclampsia.
SALL4 also outperformed PLAP on a small sample of cytology blocks. Although SALL4 is not entirely specific, it is a highly sensitive marker with strong diffuse nuclear reactivity in the majority of MGCTs in the posttreatment setting, at significantly higher levels than PLAP
Multiple negatively charged small molecules interact within the active site of ASRGL1 (show ASRGL1 ELISA Kits) to act as a base in promoting cleavage.
Reduced expression of ASRGL1 (show ASRGL1 ELISA Kits), defined as <75% positively stained tumor cells, was significantly associated with poor prognosis and reduced disease-specific survival in endometrioid endometrial adenocarcinoma (EEA).
Quantum-mechanical computational methods were employed to study the catalytic mechanism of human placental AP (PLAP). An active-site model was used, constructed on the basis of the X-ray crystal structure of the enzyme.
There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2 while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme, also referred to as the heat stable form, that is expressed primarily in the placenta although it is closely related to the intestinal form of the enzyme as well as to the placental-like form. The coding sequence for this form of alkaline phosphatase is unique in that the 3' untranslated region contains multiple copies of an Alu family repeat. In addition, this gene is polymorphic and three common alleles (type 1, type 2 and type 3) for this form of alkaline phosphatase have been well characterized.
, alkaline phosphatase Regan isozyme
, alkaline phosphatase, placental type
, alkaline phosphomonoesterase
, placental alkaline phosphatase 1
, bacterial alkaline phosphatase
, alkaline phosphatase, placental (Regan isozyme)
, C-C motif chemokine 27
, tissue-nonspecific alkaline phosphatase
, alkaline phosphatase
, alkaline phosphatase, intestinal
, PDZ and LIM domain protein 3
, actinin alpha 2 associated LIM protein
, actinin-associated LIM protein
, alpha-actinin-2-associated LIM protein