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The protein encoded by LRBA is a member of the WDL-BEACH-WD (WBW) gene family. De plus, nous expédions LRBA Protéines (8) et LRBA Kits (2) et beaucoup plus de produits pour cette protéine.
Showing 10 out of 17 products:
Human Polyclonal LRBA Primary Antibody pour ICC, IF - ABIN4331440
Lopez-Herrera, Tampella, Pan-Hammarström, Herholz, Trujillo-Vargas, Phadwal, Simon, Moutschen, Etzioni, Mory, Srugo, Melamed, Hultenby, Liu, Baronio, Vitali, Philippet, Dideberg, Aghamohammadi et al.: Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. ... dans American journal of human genetics 2012
Human Polyclonal LRBA Primary Antibody pour ICC, IF - ABIN4331442
Burns, Zenner, Plagnol, Curtis, Mok, Eisenhut, Kumararatne, Doffinger, Thrasher, Nejentsev: LRBA gene deletion in a patient presenting with autoimmunity without hypogammaglobulinemia. dans The Journal of allergy and clinical immunology 2012
As diabetes was the presenting feature in six of nine individuals, we recommend that testing for LRBA mutations is considered in all patients with newly diagnosed neonatal diabetes and in those with infancy-onset diabetes (<12 months), especially when a recessive inheritance is suspected or additional autoimmune features are present
Assessing total CTLA-4 (Montrer CTLA4 Anticorps) expression levels was found to be optimal when restricting analysis to the CD45RA(-)Foxp3 (Montrer FOXP3 Anticorps)(+) fraction. CTLA-4 (Montrer CTLA4 Anticorps) induction following stimulation, and the use of lysosomal-blocking compounds, distinguished CTLA-4 (Montrer CTLA4 Anticorps) from LRBA mutations
Case Report: potential causative role of LRBA gene mutations in juvenile arthritis.
Among 2 brothers homozygous for LPS responsive beige-like anchor protein (Montrer CELSR3 Anticorps) (LRBA) mutation, one developed Evans syndrome and deceased at age 8.5, and his brother carried the same homozygous LRBA mutation with early-onset erosive polyarthritis.
diagnosis of LRBA deficiency was confirmed by a fluorescence-activated cell sorting-based immunoassay
Variants of LRBA were associated with common variable immunodeficiency.
A homozygous missense mutation in lipopolysaccharide-responsive and beige (Montrer LYST Anticorps)-like anchor gene is associated with inflammatory bowel disease.
LRBA mutation was associated with an autoimmune lymphoproliferative syndrome-like disease characterized by splenomegaly and lymphadenopathy, cytopenia, elevated double negative T cells and raised serum Fas ligand (Montrer FASL Anticorps) levels.
Patients with LRBA deficiency manifested a dramatic and sustained improvement in response to abatacept, a CTLA4 (cytotoxic T lymphocyte antigen-4 (Montrer CTLA4 Anticorps))-immunoglobulin fusion drug.
LRBA deficiency is a novel cause of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX (Montrer FOXP3 Anticorps)) syndrome and Treg cell deficiency associated with metabolic dysfunction and increased apoptosis of Treg cells.
The protein encoded by this gene is a member of the WDL-BEACH-WD (WBW) gene family. Its expression is induced in B cells and macrophages by bacterial lipopolysaccharides (LPS). The encoded protein associates with protein kinase A and may be involved in leading intracellular vesicles to activated receptor complexes, which aids in the secretion and/or membrane deposition of immune effector molecules. Defects in this gene are associated with the disorder common variable immunodeficiency-8 with autoimmunity. Two transcript variants encoding different isoforms have been found for this gene.
, lipopolysaccharide-responsive and beige-like anchor protein
, CDC4-like protein
, vesicle trafficking, beach and anchor containing