ACCN4 anticorps (N-Term)

N° du produit ABIN5533734

Détail du produit anti-ACCN4 anticorps

Antigène: ACCN4 (Amiloride-Sensitive Cation Channel 4, Pituitary (ACCN4))

Épitope: AA 23-52, N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACCN4 est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: This ACCN4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-52 amino acids from the N-terminal region of human ACCN4.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.48 mg/mL

Buffer: 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: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur ACCN4

Antigène: ACCN4 (Amiloride-Sensitive Cation Channel 4, Pituitary (ACCN4))

Autre désignation: ACCN4 (ACCN4 Produits)

Synonymes: anticorps ACCN4, anticorps BNAC4, anticorps Accn4, anticorps Spasic, anticorps acid sensing ion channel subunit family member 4 S homeolog, anticorps acid sensing ion channel subunit family member 4, anticorps acid-sensing (proton-gated) ion channel family member 4, anticorps asic4.S, anticorps ASIC4, anticorps Asic4

Sujet: This gene belongs to the superfamily of acid-sensing ion channels, which are proton-gated, amiloride-sensitive sodium channels. These channels have been implicated in synaptic transmission, pain perception as well as mechanoperception. This gene is predominantly expressed in the pituitary gland, and was considered a candidate for paroxysmal dystonic choreoathetosis (PDC), a movement disorder, however, no correlation was found between mutations in this gene and PDC. Alternative splicing at this locus results in two transcript variants encoding different isoforms.

Poids moléculaire: 70 kDa

ID gène: 55515

UniProt: Q96FT7