APH1A Polyclonal Antibody (E-AB-65068)

For research use only.
Verified Samples |
Verified Samples in IF: L929 |
Dilution | IF 1:50-1:100 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse |
Applications | IF |
Clonality | Polyclonal |
Immunogen | A synthetic peptide of human APH1A (NP_001071096.1). |
Abbre | APH1A |
Synonyms | 6530402N02Rik, APH-1, APH-1A, APH1A, CGI-78 |
Swissprot | |
Cellular Localization | Endoplasmic reticulum membrane, Golgi apparatus, Golgi stack membrane, Predominantly located in the endoplasmic reticulum and in the cis-Golgi. |
Concentration | 1 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Cancer, Neuroscience, Stem Cells |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | This gene encodes a component of the gamma secretase complex that cleaves integral membrane proteins such as Notch receptors and beta-amyloid precursor protein. The gamma secretase complex contains this gene product, or the paralogous anterior pharynx defective 1 homolog B (APH1B), along with the presenilin, nicastrin, and presenilin enhancer-2 proteins. The precise function of this seven-transmembrane-domain protein is unknown though it is suspected of facilitating the association of nicastrin and presenilin in the gamma secretase complex as well as interacting with substrates of the gamma secretase complex prior to their proteolytic processing. Polymorphisms in a promoter region of this gene have been associated with an increased risk for developing sporadic Alzheimer's disease. Alternative splicing results in multiple protein-coding and non-protein-coding transcript variants. |
Other Clones
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Other Formats
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Unconjugated
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