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KCNQ5 Antibody (C-term) Blocking Peptide

Synthetic peptide

     
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Product Information
Primary Accession Q9NR82
Clone Names 100528235
Additional Information
Gene ID 56479
Other Names Potassium voltage-gated channel subfamily KQT member 5, KQT-like 5, Potassium channel subunit alpha KvLQT5, Voltage-gated potassium channel subunit Kv75, KCNQ5
Format Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name KCNQ5
Function Associates with KCNQ3 to form a potassium channel which contributes to M-type current, a slowly activating and deactivating potassium conductance which plays a critical role in determining the subthreshold electrical excitability of neurons. Therefore, it is important in the regulation of neuronal excitability. May contribute, with other potassium channels, to the molecular diversity of a heterogeneous population of M-channels, varying in kinetic and pharmacological properties, which underlie this physiologically important current. Insensitive to tetraethylammonium, but inhibited by barium, linopirdine and XE991. Activated by niflumic acid and the anticonvulsant retigabine. As the native M-channel, the potassium channel composed of KCNQ3 and KCNQ5 is also suppressed by activation of the muscarinic acetylcholine receptor CHRM1.
Cellular Location Cell membrane; Multi-pass membrane protein
Tissue Location Strongly expressed in brain and skeletal muscle. In brain, expressed in cerebral cortex, occipital pole, frontal lobe and temporal lobe. Lower levels in hippocampus and putamen. Low to undetectable levels in medulla, cerebellum and thalamus
Research Areas
Citations (0)
citation

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Background

This gene is a member of the KCNQ potassium channel genefamily that is differentially expressed in subregions of the brainand in skeletal muscle. The protein encoded by this gene yieldscurrents that activate slowly with depolarization and can formheteromeric channels with the protein encoded by the KCNQ3 gene.Currents expressed from this protein have voltage dependences andinhibitor sensitivities in common with M-currents. They are alsoinhibited by M1 muscarinic receptor activation. Multiple transcriptvariants encoding different isoforms have been found for this gene.

References

Bailey, S.D., et al. Diabetes Care (2010) In press :Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)Roura-Ferrer, M., et al. Cell. Physiol. Biochem. 24 (5-6), 325-334 (2009) :Bal, M., et al. J. Biol. Chem. 283(45):30668-30676(2008)

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$ 277.78
Cat# BP16776b
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