KCNE1-Like Antikörper (Middle Region)

Produktnummer ABIN953001

Dieses Anti-KCNE1-Like-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von KCNE1-Like in WB und EIA. Geeignet für Human.

Kurzübersicht für KCNE1-Like Antikörper (Middle Region) (ABIN953001)

Target: KCNE1-Like (KCNE1L)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser KCNE1-Like Antikörper ist unkonjugiert

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

Produktdetails anti-KCNE1-Like Antikörper

Bindungsspezifität: AA 74-104, Middle Region

Spezifität: This antibody recognizes Human KCE1L (Center).

Aufreinigung: Protein A column, followed by peptide affinity purification

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

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

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

Details zu KCNE1-Like

Target: KCNE1-Like (KCNE1L)

Andere Bezeichnung: KCNE1L

Hintergrund: 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

Molekulargewicht: 14993 Da

Gen-ID: 23630

NCBI Accession: NP_036414