|Positive WB detected in||human spleen tissue, PC-3 cells, RAW 264.7 cells|
|Western Blot (WB)||WB : 1:500-1:1000|
|Sample-dependent, check data in validation data gallery|
10980-1-AP targets Fc Epsilon RI Alpha in WB, IHC, IF, ELISA applications and shows reactivity with human, mouse samples.
|Tested Reactivity||human, mouse|
|Cited Reactivity||human, mouse|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Fc Epsilon RI Alpha fusion protein Ag1398|
|Full Name||Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide|
|Calculated molecular weight||30 kDa|
|Observed molecular weight||55 kDa|
|GenBank accession number||BC015195|
|Gene ID (NCBI)||2205|
|Purification Method||Antigen affinity purification|
|Storage Buffer||PBS with 0.02% sodium azide and 50% glycerol pH 7.3.|
|Storage Conditions||Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.|
Fc fragment of IgE, high affinity I, receptor for, alpha polypeptide, also known as high affinity immunoglobulin epsilon receptor subunit alpha, FCER1A and FCE1A, is a single-pass type I membrane protein which contains 2 immunoglobulin-like domains. FCER1A is a subunit of the IgE receptor, which is composed of one glycosylated alpha (FCER1A), one beta (FCER1B), and two gamma (FCER1G) subunits. The high affinity IgE receptor plays a central role in allergic disease, coupling allergen and mast cell to initiate the inflammatory and immediate hypersensitivity responses that are characteristic of disorders such as hay fever and asthma.
Alveolar mast cells shift to an FcεRI-expressing phenotype in mild atopic asthma: a novel feature in allergic asthma pathology.
Novel site-specific mast cell subpopulations in the human lung.
Elevated IgE promotes cardiac fibrosis by suppressing miR-486a-5p.
J Allergy Clin Immunol
Thymic stromal lymphopoietin epigenetically upregulates Fc receptor γ subunit-related receptors on antigen-presenting cells and induces TH2/TH17 polarization through dectin-2.
J Allergy Clin Immunol
Mast cell-associated alveolar inflammation in patients with atopic uncontrolled asthma.
Response to Comment on "Tumor-initiating cells establish an IL-33-TGF-β niche signaling loop to promote cancer progression".