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  • mProX™ Human KCNA4 Stable Cell Line

    [CAT#: S01YF-1123-KX18]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Ion Channel Cell Lines

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    Product Information

    Target Protein
    KCNA4
    Target Family
    Kv1
    Target Protein Species
    Human
    Host Cell Type
    CHO-K1; HEK293
    Target Classification
    Ion Channel Cell Lines
    Target Research Area
    Cardiovascular Research; CNS Research; Digestive and Renal Research
    Related Diseases
    Microcephaly; Cataracts; Impaired Intellectual Development; Dystonia
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Subfamily of potassium voltage-gated channels The KCNA4 gene in humans produces the protein known as A member 4 (also known as Kv1.4). It contributes to the cardiac transient outward potassium current (Ito1), which is a key current in the cardiac action potential's repolarizing phase 1. They control a variety of processes, including smooth muscle contraction, insulin secretion, neuronal excitability, neurotransmitter release, heart rate, and cell volume. It is a member of the A-type potassium current class, whose members may be crucial in controlling the fast repolarizing phase of cardiac action potentials, which may have an impact on how long they last. The customized KCNA4 stable cell line can be used in antibody discovery and development, potential drug candidate screening and signaling pathway researches.

    Protocols

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    Customer Reviews

    chat Thomas

    The Human KCNA4 Stable Cell Line is very good! Sep 12 2021

    chat Verified Customer

    chat Joseph

    The KCNA4 Stable Cell Line is great for ion channel research. May 11 2023

    chat Verified Customer

    FAQ

    Any questions about our products? Please visit our frequently asked questions page.

    Published Data

    Fig.1 Schematic illustration of KCNA4.

    With only one open reading frame and two transcripts produced, only one of KCNA4's transcripts is translated into a protein. The model includes a number of domains, including superfamily domains, low complexity segments, and transmembrane helices.

    Ref: Kaya, Namik, et al. "KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability." Journal of medical genetics 53.11 (2016): 786-792.

    Pubmed: 27582084

    DOI: 10.1136/jmedgenet-2015-103637

    Research Highlights

    From a structural and functional standpoint, voltage-gated potassium channels are an extremely diverse class of voltage-gated ion channels represented by very complex proteins. Many human illnesses are typically the result of these channels being deficient.
    Kaya, Namik, et al. "KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability." Journal of medical genetics 53.11 (2016): 786-792.
    Pubmed: 27582084   DOI: 10.1136/jmedgenet-2015-103637

    Nucleoporins (Nups) are essential for cell-type-specific gene regulation, as evidence is mounting; however, it is not yet known how they regulate the expression and function of ion channel genes in the heart.
    Gao, Xueting, et al. "Nucleoporin 50 mediates Kcna4 transcription to regulate cardiac electrical activity." Journal of cell science 134.18 (2021): jcs256818.
    Pubmed: 34409458   DOI: 10.1242/jcs.256818

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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