• Western blot analysis of the lysates from HepG2 cells using KCNA1 antibody.
  • Western blot analysis of HeLa cells using KV1.1 Polyclonal Antibody diluted at 1:2000
  • Western blot analysis of lysates from HUVEC, MCF-7, and HeLa cells, using KCNA1 Antibody. The lane on the right is blocked with the synthesized peptide.
  • Western blot analysis of various cells using KV1.1 Polyclonal Antibody diluted at 1:2000

Anti-KCNA1 antibody (256-305 aa) (STJ93870)

SKU:
STJ93870

Current Stock:
Host: Rabbit
Applications: WB/ELISA/IHC
Reactivity: Human/Mouse/Rat
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit polyclonal antibody anti-Potassium voltage-gated channel subfamily A member 1 channel HuKI (256-305 aa) is suitable for use in Western Blot, ELISA and Immunohistochemistry research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: Liquid in PBS containing 50% Glycerol, 0.5% BSA and 0.02% Sodium Azide.
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/mL
Dilution Range: WB 1:500-2000
IHC-P 1:50-300
ELISA 2000-20000
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: KCNA1
Gene ID: 3736
Uniprot ID: KCNA1_HUMAN
Immunogen Region: 256-305 aa
Specificity: KV1.1 Polyclonal Antibody detects endogenous levels of KV1.1 protein.
Immunogen: The antiserum was produced against synthesized peptide derived from the human KCNA1 at the amino acid range 256-305
Post Translational Modifications 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. Phosphorylation at Ser-446 regulates channel activity by down-regulating expression at the cell membrane.
Function Voltage-gated potassium channel that mediates transmembrane potassium transport in excitable membranes, primarily in the brain and the central nervous system, but also in the kidney. Contributes to the regulation of the membrane potential and nerve signaling, and prevents neuronal hyperexcitability. Forms tetrameric potassium-selective channels through which potassium ions pass in accordance with their electrochemical gradient. The channel alternates between opened and closed conformations in response to the voltage difference across the membrane. Can form functional homotetrameric channels and heterotetrameric channels that contain variable proportions of KCNA1, KCNA2, KCNA4, KCNA5, KCNA6, KCNA7, and possibly other family members as well.channel properties depend on the type of alpha subunits that are part of the channel. Channel properties are modulated by cytoplasmic beta subunits that regulate the subcellular location of the alpha subunits and promote rapid inactivation of delayed rectifier potassium channels. In vivo, membranes probably contain a mixture of heteromeric potassium channel complexes, making it difficult to assign currents observed in intact tissues to any particular potassium channel family member. Homotetrameric KCNA1 forms a delayed-rectifier potassium channel that opens in response to membrane depolarization, followed by slow spontaneous channel closure. In contrast, a heterotetrameric channel formed by KCNA1 and KCNA4 shows rapid inactivation. Regulates neuronal excitability in hippocampus, especially in mossy fibers and medial perforant path axons, preventing neuronal hyperexcitability. Response to toxins that are selective for KCNA1, respectively for KCNA2, suggests that heteromeric potassium channels composed of both KCNA1 and KCNA2 play a role in pacemaking and regulate the output of deep cerebellar nuclear neurons. May function as down-stream effector for G protein-coupled receptors and inhibit GABAergic inputs to basolateral amygdala neurons. May contribute to the regulation of neurotransmitter release, such as gamma-aminobutyric acid (GABA) release. Plays a role in regulating the generation of action potentials and preventing hyperexcitability in myelinated axons of the vagus nerve, and thereby contributes to the regulation of heart contraction. Required for normal neuromuscular responses. Regulates the frequency of neuronal action potential firing in response to mechanical stimuli, and plays a role in the perception of pain caused by mechanical stimuli, but does not play a role in the perception of pain due to heat stimuli. Required for normal responses to auditory stimuli and precise location of sound sources, but not for sound perception. The use of toxins that block specific channels suggest that it contributes to the regulation of the axonal release of the neurotransmitter dopamine. Required for normal postnatal brain development and normal proliferation of neuronal precursor cells in the brain. Plays a role in the reabsorption of Mg(2+) in the distal convoluted tubules in the kidney and in magnesium ion homeostasis, probably via its effect on the membrane potential.
Protein Name Potassium Voltage-Gated Channel Subfamily A Member 1
Voltage-Gated K(+ Channel Huki
Voltage-Gated Potassium Channel Hbk1
Voltage-Gated Potassium Channel Subunit Kv1.1
Database Links Reactome: R-HSA-1296072
Cellular Localisation Cell Membrane
Multi-Pass Membrane Protein
Membrane
Cell Projection
Axon
Cytoplasmic Vesicle
Perikaryon
Endoplasmic Reticulum
Dendrite
Cell Junction
Synapse
Presynaptic Cell Membrane
Presynapse
Homotetrameric Kcna1 Is Primarily Located In The Endoplasmic Reticulum
Interaction With Kcna2 And Kcnab2 Or With Kcna4 And Kcnab2 Promotes Expression At The Cell Membrane
Alternative Antibody Names Anti-Potassium Voltage-Gated Channel Subfamily A Member 1 antibody
Anti-Voltage-Gated K(+ Channel Huki antibody
Anti-Voltage-Gated Potassium Channel Hbk1 antibody
Anti-Voltage-Gated Potassium Channel Subunit Kv1.1 antibody
Anti-KCNA1 antibody

Information sourced from Uniprot.org

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