Skip to content

Datenblatt ansehen

open_in_new
  1. Alles ansehen
  2. Polyclonal

GTX16690

KCNE3 antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX16690
Zusätzliche Namen:
potassium voltage-gated channel subfamily E regulatory subunit 3 , BRGDA6 , HOKPP , HYPP , MiRP2
Anwendung:
IHC, WB, IF, ICC
Konzentration:
0.8 mg/ml
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:
Genetex
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Buffer:
PBS, 1% BSA, 0.025% Sodium azide.
Immunogen:
Peptide (C)RSRKVDKRSDPYH, corresponding to amino acid residues 81-93 (Intracellular, C-terminal part) of human KCNE3 (Accession : Q9Y6H6).
Uniprot:
Q9Y6H6
Synonyme:
BRGDA6;cardiac voltage-gated potassium channel accessory subunit;HOKPP;HYPP;minimum potassium ion channel-related peptide 2;minK-related peptide 2;MiRP2;potassium channel subunit beta MiRP2;potassium channel, voltage gated subfamily E regulatory beta subunit 3;potassium voltage-gated channel subfamily E member 3;potassium voltage-gated channel, Isk-related family, member 3;voltage-gated K+ channel subunit MIRP2
Weitere Details:
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 member of the potassium channel, voltage-gated, isk-related subfamily. This member is a type I membrane protein, and a beta subunit that assembles with a potassium channel alpha-subunit to modulate the gating kinetics and enhance stability of the multimeric complex. This gene is prominently expressed in the kidney. A missense mutation in this gene is associated with hypokalemic periodic paralysis. [provided by RefSeq, Jul 2008]
Versandbedingungen:
Blue Ice