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PEPD encodes a member of the peptidase family. Additionally we are shipping Peptidase D Kits (21) and Peptidase D Proteins (10) and many more products for this protein.
Showing 10 out of 49 products:
Cow (Bovine) Polyclonal PEPD Primary Antibody for WB - ABIN2786507
Surazynski, Donald, Cooper, Whiteside, Salnikow, Liu, Phang: Extracellular matrix and HIF-1 signaling: the role of prolidase. in International journal of cancer. Journal international du cancer 2008
High resolution X-ray crystallographic models of substrate and product binding in the active site of human prolidase.
We report here that by introducing either the A252R or P365R substitution mutation, the structural changes affecting catalytic turnover rate and substrate binding affinity are valuable in improving the catalytic activity of human prolidase towards toxic organophosphorus compound hydrolysis.
In ankylosing spondylitis, serum prolidase level was successful in measuring disease activity
there is an independent relationship of aortic prolidase activity and aortic prolidase immunostaining with aortic stiffness beta index in patients who underwent coronary artery bypass grafting
Prolidase activity decreases in patients with chronic obstructive pulmonary disease.
absence of prolidase activity in pterygium tissue indicates that there is no collagen turnover in this tissue
Decreased serum prolidase activity may be associated with knee osteoarthritis
The association between the PEPD genetic variant and the risk of T2D was modulated by n-3 fatty acids. Higher n-3 fatty acids may abolish the adverse effect of the risk allele at PEPD for T2D
Prolidase was required for IFNAR1 (show IFNAR1 Antibodies) maturation and accumulation, activation of IFNbeta-stimulated gene induction, and IFN-I-dependent viral control.
Levels of both serum prolidase and AFP (show AFP Antibodies) could contribute to the early diagnosing of hepatocellular carcinoma.
The findings identify peptidase D, an ubiquitously expressed intracellular peptidase, as a potential novel marker of colitis.
PEPD is a ligand of EGFR (show EGFR Antibodies) and presents a novel mechanism of EGFR (show EGFR Antibodies) activation
The dark-like mutation causes cardiomyocyte hypertrophy due to loss-of-function of peptidase d (Pepd).
NO stimulates prolidase activity by increasing serine/threonine phosphorylation through PKG (show PRKG1 Antibodies)-cGMP pathway
This gene encodes a member of the peptidase family. The protein forms a homodimer that hydrolyzes dipeptides or tripeptides with C-terminal proline or hydroxyproline residues. The enzyme serves an important role in the recycling of proline, and may be rate limiting for the production of collagen. Mutations in this gene result in prolidase deficiency, which is characterized by the excretion of large amount of di- and tri-peptides containing proline. Multiple transcript variants encoding different isoforms have been found for this gene.
, X-Pro dipeptidase
, aminoacyl-L-proline hydrolase
, proline dipeptidase
, xaa-Pro dipeptidase
, X-pro dipeptidase
, peptidase 4