Gephyrin anticorps (AA 148-736)

N° du produit ABIN7870771

Cet anticorps anti-Gephyrin Polyclonal Lapin (ABIN7870771) détecte spécifiquement Gephyrin dans WB, ELISA, IF et IHC (p). L’anticorps est réactif avec des échantillons de Humain, Souris, Rat et Singe.

Aperçu rapide pour Gephyrin anticorps (AA 148-736) (ABIN7870771)

Antigène: Gephyrin (GPHN)

Reactivité: Humain, Souris, Rat, Singe

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Gephyrin est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-Gephyrin anticorps

Épitope: AA 148-736

Fonction: Gephyrin Antibody / GPHN

Purification: Affinity purified

Immunogène: An E. coli-derived human protein (amino acids K148-L736) was used as the immunogen for the Gephyrin antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Gephyrin antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the Gephyrin antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur Gephyrin

Antigène: Gephyrin (GPHN)

Autre désignation: Gephyrin

Sujet: Gephyrin is a protein that in humans is encoded by the GPHN gene. This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described, however, the full-length nature of all transcript variants is not currently known.

UniProt: Q9NQX3

Pathways: Synaptic Membrane, Skeletal Muscle Fiber Development