KCNN3 Antibody Blocking Peptide(bs-11569P)-500ug

KCNN3 Antibody Blocking Peptid

e(bs-11569P)-500ug
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  • bs-11569P
  • 2025年10月16日
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      500ug

    产品编号bs-11569P
    英文名称KCNN3 Antibody Blocking Peptide
    中文名称钙激活钾通道蛋白3封闭多肽
    英文别名hSK3; KCa2.3; Kcnn3; KCNN3_HUMAN; Potassium intermediate/small conductance calcium activated channel subfamily N member 3; SK3; SKCa 3; SKCa3; Small conductance calcium-activated potassium channel protein 3.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurology process > Neural Signal Transduction

    Neuroscience > Neurotransmission > Receptors / Channels > Potassium Channels

    亚基Heterooligomer. The complex is composed of 4 channel subunits each of which binds to a calmodulin subunit which regulates the channel activity through calcium-binding
    亚细胞定位Membrane; Multi-pass membrane protein.
    相似性Belongs to the potassium channel KCNN family. KCa2.3/KCNN3 subfamily.
    功能Forms a voltage-independent potassium channel activated by intracellular calcium. Activation is followed by membrane hyperpolarization. Thought to regulate neuronal excitability by contributing to the slow component of synaptic afterhyperpolarization. The channel is blocked by apamin.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. This gene belongs to the KCNN family of potassium channels. It encodes an integral membrane protein that forms a voltage-independent calcium-activated channel, which is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene contains two CAG repeat regions in the coding sequence. It was thought that expansion of one or both of these repeats could lead to an increased susceptibility to schizophrenia or bipolar disorder, but studies indicate that this is probably not the case. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]

     

     

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