KCNE1-Like Antikörper (AA 67-96)

Produktnummer ABIN653619

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

Kurzübersicht für KCNE1-Like Antikörper (AA 67-96) (ABIN653619)

Target: KCNE1-Like (KCNE1L)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser KCNE1-Like Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: RB24387

Produktdetails anti-KCNE1-Like Antikörper

Bindungsspezifität: AA 67-96

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

Immunogen: This KCE1L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 67-96 amino acids from the Central region of human KCE1L.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Haltbarkeit: 6 months

Details zu KCNE1-Like

Target: KCNE1-Like (KCNE1L)

Andere Bezeichnung: KCE1L

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.

Molekulargewicht: 14993

Gen-ID: 23630

NCBI Accession: NP_036414

UniProt: Q9UJ90