Anti-FCER1G antibody (ab108228)
- Product nameAnti-FCER1G antibodySee all FCER1G primary antibodies ...
- DescriptionRabbit polyclonal to FCER1G
- Tested applicationsWB more details
- Species reactivityReacts with: Human
Synthetic peptide corresponding to a region within N terminal amino acids 1-50 (MIPAVVLLLL LLVEQAAALG EPQLCYILDA ILFLYGIVLT LLYCRLKIQV) of Human FCER1G (NP_004097).
- Positive controlHeLa cell lysate
- Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.
- Storage bufferPreservative: None
Constituents: 2% Sucrose, PBS
- Concentration information loading...
- PurityImmunogen affinity purified
- Clonality Polyclonal
- Research Areas
Our Abpromise guarantee covers the use of ab108228 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||WB: Use a concentration of 1 µg/ml. Predicted molecular weight: 10 kDa. Good results were obtained when blocked with 5% non-fat dry milk in 0.05% PBS-T.|
- FunctionAssociates with a variety of FcR alpha chains to form a functional signaling complex. Regulates several aspects of the immune response. The gamma subunit has a critical role in allowing the IgE Fc receptor to reach the cell surface.
- Sequence similaritiesBelongs to the CD3Z/FCER1G family.
Contains 1 ITAM domain.
- Cellular localizationCell membrane.
- Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide antibodyFc receptor gamma chain antibodyFc-epsilon RI-gamma antibody
- FCER1G antibodyFCERG_HUMAN antibodyFceRI gamma antibodyFCRG antibodyFcRgamma antibodyHigh affinity immunoglobulin epsilon receptor subunit gamma antibodyIgE Fc receptor subunit gamma antibodyImmunoglobulin E receptor, high affinity, gamma chain antibody
Anti-FCER1G antibody images
Anti-FCER1G antibody (ab108228) at 1 µg/ml + HeLa cell lysate at 10 µg
Predicted band size : 10 kDa
References for Anti-FCER1G antibody (ab108228)
ab108228 has not yet been referenced specifically in any publications.