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anti-Mouse (Murine) PLA2R1 Antikörper:
anti-Human PLA2R1 Antikörper:
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Human Polyclonal PLA2R1 Primary Antibody für IHC, IHC (p) - ABIN4345962
Debiec, Ronco: PLA2R autoantibodies and PLA2R glomerular deposits in membranous nephropathy. in The New England journal of medicine 2011
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Human Polyclonal PLA2R1 Primary Antibody für WB - ABIN4345961
Silliman, Moore, Zallen, Gonzalez, Johnson, Elzi, Meng, Hanasaki, Ishizaki, Arita, Ao, England, Banerjee: Presence of the M-type sPLA(2) receptor on neutrophils and its role in elastase release and adhesion. in American journal of physiology. Cell physiology 2002
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Human Polyclonal PLA2R1 Primary Antibody für ELISA, IF - ABIN347711
Hoxha, Harendza, Zahner, Panzer, Steinmetz, Fechner, Helmchen, Stahl: An immunofluorescence test for phospholipase-A2-receptor antibodies and its clinical usefulness in patients with membranous glomerulonephritis. in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2011
PLA2R1 is increased in the airway epithelium in asthma, and serves as a regulator of airway hyperresponsiveness, airway permeability, antigen sensitization, and airway inflammation.
Study showed that CTLD1-2 as well as the FNII domain of PLA2R were responsible for binding to collagen I and collagen-dependent migration in both mouse and human PLA2R.
PLA2R might play a pathogenic role in myocardial infarction of PLA2R-deficient mice, through impaired healing of the infarcted region.
PLA2R deficiency increased sPLA2 (zeige PLA2G2A Antikörper)-IB and -X levels in the lung through their impaired clearance from the lung, leading to exaggeration of lung inflammation induced by OVA treatment in a murine model.
Compared with non-PLA2R-associated IMN patients in our cohort, PLA2R-associated IMN patients presented with more severe proteinuria and lower remission rates after treatment, with no distinct histological differences.
Suggest strong genetic association between nonsynonymous SNP rs35771982 (p.His300Asp) within PLA2R1 and idiopathic membranous nephropathy.
We propose a revised clinical workup flow for patients with MN that recommends assessment of kidney biopsy for PLA2R1 and THSD7A (zeige THSD7A Antikörper) antigen expression, screening for circulating anti-podocytes antibodies, and assessment for secondary causes, especially cancer, in patients with THSD7A (zeige THSD7A Antikörper) antibodies
Five SNPs around the PLA2R1 gene were significantly associated with idiopathic membranous nephropathy.
Several risk alleles related to the PLA2R1 gene and within the HLA loci have been identified, whereas epitope spreading of PLA2R may predict treatment response. More recently, thrombospondin type 1 domain-containing 7A (THSD7A (zeige THSD7A Antikörper)) antibodies have been discovered in primary membranous nephropathy .
PLA2R may play a role in some adolescent and preteen idiopathic membranous nephropathy patients but may be less frequently associated with idiopathic membranous nephropathy during childhood
Anti-M-type phospholipase A2 (zeige YWHAZ Antikörper) receptor (anti-PLA2R) and anti-THSD7A (zeige THSD7A Antikörper) (thrombospondin type-1 domain-containing 7A) were detected only in membranous neurophathy (MN) patient sera and not in controls.
The frameshift mutation detected in the current study would result in premature stops of amino acid synthesis in PLA2R1 and SRPK1 (zeige SRPK1 Antikörper) proteins and hence resembles a typical inactivating mutation.
Single-nucleotide polymorphism in PLA2R1 gene is associated with primary membranous nephropathy.
blocking the ERRalpha (zeige ESRRA Antikörper)-controlled mitochondrial program largely inhibits the PLA2R1-induced tumor-suppressive response. Together, our data document ERRalpha (zeige ESRRA Antikörper) and its mitochondrial program as downstream effectors of the PLA2R1-JAK2 (zeige JAK2 Antikörper) pathway leading to oncosuppression.
This gene represents a phospholipase A2 receptor. The encoded protein likely exists as both a transmembrane form and a soluble form. The transmembrane receptor may play a role in clearance of phospholipase A2, thereby inhibiting its action. Polymorphisms at this locus have been associated with susceptibility to idiopathic membranous nephropathy. Alternatively spliced transcript variants encoding different isoforms have been identified.
phospholipase A2 receptor 1, 180kDa
, 180 kDa secretory phospholipase A2 receptor
, M-type receptor
, PLA2-I receptor
, phospholipase A2, group IB, pancreas, receptor
, secretory phospholipase A2 receptor
, C-type lectin domain family 13 member C