KCNE1-Like anticorps (N-Term)

N° du produit ABIN5516923

Détail du produit anti-KCNE1-Like anticorps

Antigène: KCNE1-Like (KCNE1L)

Épitope: N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KCNE1-Like est non-conjugé

Application: Western Blotting (WB)

Séquence: RLRTLLSRLL LELHHRGNAS GLGAGPRPSM GMGVVPDPFV GREVTSAKGD

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human KCNE1L

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur KCNE1-Like

Antigène: KCNE1-Like (KCNE1L)

Autre désignation: KCNE1L (KCNE1L Produits)

Synonymes: anticorps KCNE1L, anticorps KCNE5, anticorps Kcne5, anticorps potassium voltage-gated channel subfamily E regulatory subunit 5, anticorps KCNE5, anticorps Kcne5

Sujet: Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a membrane protein which has sequence similarity to the KCNE1 gene product, a member of the potassium channel, voltage-gated, isk-related subfamily. This intronless gene is deleted in AMME contiguous gene syndrome and may be involved in the cardiac and neurologic abnormalities found in the AMME contiguous gene syndrome.

Alias Symbols: KCNE1L

Protein Size: 167

ID gène: 23630

NCBI Accession: NM_012282, NP_036414

UniProt: Q9UJ90