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EPX is a member of the peroxidase gene family and is expressed in eosinophils. Additionally we are shipping EPX Antibodies (66) and EPX Kits (16) and many more products for this protein.
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tyrosine phosphorylation of PMR1 (show ATP2C1 Proteins) is required for the targeting and degradation of polyribosome-bound substrate mRNA
there is a strong association in a given patient between both nasal and pharyngeal EPX levels and the eosinophil percentage of induced sputum.
Myeloperoxidase (show MPO Proteins) and eosinophil peroxidase are readily internalized by HUVEC cells where they promote cellular proliferation, migration, invasion, and stimulate angiogenesis both in vitro and in vivo.
A preferential role of EPO (show EPO Proteins) signaling via a specific surface receptor that leads to neural plasticity.
Eosinophil peroxidase in sputum represents a unique biomarker of airway eosinophilia.
report the prevalence of a common SNP in the eosinophil protein x/eosinophil-derived neurotoxin (show RNASE2 Proteins) (EPX/EDN (show RNASE2 Proteins), RNase2 (show RNASE2 Proteins)) and the association with the cellular contents of EPX/EDN (show RNASE2 Proteins) and ECP (show ECP Proteins)
Polymorphisms of EPX and ECP (show ECP Proteins) are associated to inflammatory bowel disease in an age and gender dependent manne.
Data indicate that eosinophil peroxidase (EPX)-based ELISA is the only eosinophil-specific assay.
A mechanism of induction of ASIC-3 (show ACCN3 Proteins) expression relevant to AR was suggested by the finding that eosinophil peroxidase (EPO), acting via ERK1/2, induced the expression of ASIC-3 (show ACCN3 Proteins) in epithelial cells.
HER2 (show ERBB2 Proteins) was identified as a novel mediator of eosinophil peroxidase signaling. Eosinophil peroxidase, at noncytotoxic levels, can drive cell-cycle progression and proliferation.
EPO (show EPO Proteins)-dependent oxidative damage may play a role in tissue injury in bisulfite-exacerbated eosinophilic inflammatory disorders
The absence of MBP-1 (show ENO1 Proteins) and EPX promoted a concomitant loss of eosinophil lineage-committed progenitors in the marrow, identifying a specific blockade in eosinophilopoiesis as the causative event.
Host protection against Brugia pahangi infections was unimpaired in mice deficient in eosinophil peroxidase.
Mice deficient for either eosinophil peroxidase or major basic protein on the 129/SvJ background developed significantly higher worm burdens than wild-type mice.
post-translational tyrosine nitration of eosinophil granule toxins mediated by eosinophil peroxidase
The activities of EPO (show EPO Proteins), an eosinophilic secondary granule protein, do not affect the development of allergic pulmonary pathologies in the mouse lung at levels comparable to those observed in humans with asthma.
This gene is a member of the peroxidase gene family and is expressed in eosinophils. The encoded precursor protein is processed into covalently attached heavy and light chains to form the mature enzyme, which functions as an oxidant. The enzyme is released at sites of parasitic infection or allergen stimulation to mediate lysis of protozoa or parasitic worms. The gene is found in a cluster of three peroxidase genes at chromosome 17q23. Mutations in this gene result in eosinophil peroxidase deficiency.
, polysomal ribonuclease 1
, eosinophil peroxidase-like