Gephyrin anticorps (AA 437-466)

N° du produit ABIN653742

Détail du produit anti-Gephyrin anticorps

Antigène: Gephyrin (GPHN)

Épitope: AA 437-466

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Gephyrin est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Homologie: C, Rat

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This GPHN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 437-466 amino acids from the Central region of human GPHN.

Clone: RB24625

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Gephyrin

Antigène: Gephyrin (GPHN)

Autre désignation: GPHN (GPHN Produits)

Synonymes: anticorps 5730552E08Rik, anticorps AI662856, anticorps BC027112, anticorps C230040D23, anticorps GPH, anticorps GPHRYN, anticorps geph, anticorps Geph, anticorps GPHN, anticorps GEPH, anticorps HKPX1, anticorps gpgb1, anticorps DKFZp459M0825, anticorps gephyrin, anticorps gephyrin L homeolog, anticorps gephyrin a, anticorps Gphn, anticorps GPHN, anticorps gphn.L, anticorps gphna, anticorps PTRG_08978, anticorps VDBG_00775, anticorps Tsp_03043, anticorps gphn

Sujet: GPHN 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.

Poids moléculaire: 79748

ID gène: 10243

NCBI Accession: NP_001019389, NP_065857

UniProt: Q9NQX3

Pathways: Synaptic Membrane, Skeletal Muscle Fiber Development