KCNE1-Like anticorps (Middle Region)

N° du produit ABIN953001

Cet anticorps anti-KCNE1-Like est un anticorps Lapin Polyclonal détectant KCNE1-Like dans WB et EIA. Adapté pour Humain.

Aperçu rapide pour KCNE1-Like anticorps (Middle Region) (ABIN953001)

Antigène: KCNE1-Like (KCNE1L)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KCNE1-Like est non-conjugé

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

Détail du produit anti-KCNE1-Like anticorps

Épitope: AA 74-104, Middle Region

Specificité: This antibody recognizes Human KCE1L (Center).

Purification: Protein A column, followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 74~104 amino acids from the Central region of Human KCE1L

Isotype: Ig Fraction

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur KCNE1-Like

Antigène: KCNE1-Like (KCNE1L)

Autre désignation: KCNE1L

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.Synonyms: AMME syndrome candidate gene 2 protein, AMMECR2 protein, Potassium voltage-gated channel subfamily E member 1-like protein

Poids moléculaire: 14993 Da

ID gène: 23630

NCBI Accession: NP_036414