APH1A anticorps (N-Term)

N° du produit ABIN499307

L’anticorps anti-APH1A Polyclonal Lapin est utilisé pour la détection de APH1A dans des échantillons de Humain et Souris. Il a été validé pour WB et EIA.

Aperçu rapide pour APH1A anticorps (N-Term) (ABIN499307)

Antigène: APH1A (Anterior Pharynx Defective 1 Homolog A (C. Elegans) (APH1A))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp APH1A est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-APH1A anticorps

Épitope: N-Term

Specificité: This antibody reacts to APH1a.

Purification: Affinity chromatography purified via peptide column

Immunogène: APH1 antibody was raised against a 13 amino acid peptide from near the amino terminus of human APH1a.

Isotype: IgG

Information d'application

Indications d'application: ELISA. Western Blot: APH1 antibody can be used for detection of APH1 at 0.5 - 1 μg/mL.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Buffer: PBS containing 0.02 % sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C.

Détails sur APH1A

Antigène: APH1A (Anterior Pharynx Defective 1 Homolog A (C. Elegans) (APH1A))

Autre désignation: APH1A

Sujet: APH1 was initially identified as a component of the Notch pathway in C. elegans. Along with nicastrin, PEN2, and presenilin-1 APH1 is an essential component of the γsecretase complex which cleave the amyloid precursor protein (APP) at what are known as the gamma and epsilon sites and can lead to the accumulation of the Amyloid beta peptide A beta cleavage product that is associated with Alzheimer's disease. APH1 exists in at least three distinct isoforms with APH1alpha as the principal isoform present in the gamma secretase complex. Mice deficient in this isoform, but not the other two, were lethal at E10.5, with impaired vascular and neural development observed. Despite its predicted molecular weight, APH1 protein often migrates at aberrant locations in SDS-PAGE.Synonyms: APH-1A, Aph-1 alpha, CGI-78, Gamma-secretase subunit APH-1A, PSF, Presenilin-stabilization factor

ID gène: 51107

UniProt: Q96BI3

Pathways: Signalisation Notch, Neurotrophin Signaling Pathway