Recombinant Rabbit monoclonal primary
Recombinant Kv1.1 potassium channel Monoclonal Antibody (ET1611-7)
Human brain tissue lysates, rat brain tissue.
Store at +4C after thawing. Aliquot store at -20C or -80C. Avoid repeated freeze / thaw cycles.
1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Protein A affinity purified.
Kv1.1 potassium channel
AEMK antibody; EA1 antibody; Episodic ataxia with myokymia antibody; HBK1 antibody; HUK1 antibody; Kca1 1 antibody; Kcna1 antibody; KCNA1_HUMAN antibody; Kcpvd antibody; KV1.1 antibody; MBK1 antibody; mceph antibody; MGC124402 antibody; MGC126782 antibody; MGC138385 antibody; MK1 antibody; MK1, mouse, homolog of KV1.1 antibody; Potassium channel protein 1 antibody; Potassium voltage gated channel shaker related subfamily member 1 antibody; Potassium voltage gated channel subfamily A member 1 antibody; Potassium voltage gated channel, shaker related subfamily, member 1 (episodic ataxia with myokymia) antibody; Potassium voltage-gated channel subfamily A member 1 antibody; RBK1 antibody; RCK1 antibody; Shak antibody; Shaker related subfamily member 1 antibody; Voltage gated potassium channel subunit Kv1.1 antibody; Voltage-gated K(+) channel HuKI antibody; Voltage-gated potassium channel HBK1 antibody; Voltage-gated potassium channel subunit Kv1.1 antibody
Belongs to the potassium channel family. A (Shaker) (TC 1.A.1.2) subfamily. Kv1.1/KCNA1 sub-subfamily.
Detected adjacent to nodes of Ranvier in juxtaparanodal zones in spinal cord nerve fibers, but also in paranodal regions in some myelinated spinal cord axons (at protein level). Detected in the islet of Langerhans.
N-glycosylated.; Palmitoylated on Cys-243; which may be required for membrane targeting.; Phosphorylated on tyrosine residues. Phosphorylation increases in response to NRG1; this inhibits channel activity (By similarity). Phosphorylation at Ser-446 regulates channel activity by down-regulating expression at the cell membrane.
Cell membrane, Membrane, Cytoplasmic vesicle, Perikaryon, Endoplasmic reticulum.
Voltage-gated K+ channels in the plasma membrane control the repolarization and the frequency of action potentials in neurons, muscles, and other excitable cells. The KV gene family encodes more than 30 genes that comprise the subunits of the K+ channels, and they vary in their gating and permeation properties, subcellular distribution, and expression patterns. Functional KV channels assemble as tetramers consisting of pore-forming -subunits (KVα), which include the KV1, KV2, KV3, and KV4 proteins, and accessory or KVβ subunits that modify the gating properties of the coexpressed KVα subunits. Differences exist in the patterns of trafficking, biosynthetic processing and surface expression of the major KV1 subunits (KV1.1, KV1.2, KV1.4, KV1.5 and KV1.6) expressed in rat and human brain, suggesting that the individual protein subunits are highly regulated to control for the assembly and formation of functional neuronal channels.