santa cruz biotechnology, inc.
goat polyclonal IgG, 200µg/ml epitope mapping at the C-terminus of Aph-1b of human origin recommended for detection of Aph-1b of mouse, rat and human origin by WB, IF and ELISA; may cross-react with Aph-1c in mice; also reactive with additional species, including canine and porcine blocking peptide, sc-49358 P
Conditions Générales
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Espèce
Nom du Gène
Gene ID
Localisation chromosomique
Numéro d'accession de l'isoforme (ARNm)
Numéro d'accession de la protéine
Numéro OMIM™
Humain
APH1B
83464
15q22.2
NM_031301
Q8WW43
607630
Souris
Aph1b
208117
9 C
Q8C7N7
Non disponible
Aph-1b Background Information Anterior pharynx defective 1 (Aph-1) is a polytopic, seven-pass membrane protein that functions as one of the four essential components in the presenilin-©-secretase enzyme complex. This enzyme complex is necessary for the intra-membrane proteolysis of several different membrane proteins, including the ∫-Amyloid precursor protein, and is involved in multiple neurodevelopmental signaling pathways. Aph-1b and Aph-1a are splice variants of Aph-1. Aph-1b specifically lacks exon 4, which encodes for the entire fourth transmembrane domain, causing the protein to be destabilized. Deficiency of Aph-1a causes a reduction in ©-secretase activity, however deficiency of Aph-1b does not; thus, Aph-1b may execute redundant functions in the cell. Aph-1b expression and ©-secretase activity may be implicated in neurodevelopmental disorders, such as schizophrenia.