CYL3043 - PrecisION™ hKv3.1-CHO Recombinant Stable Cell Line

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CYL3043
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    Recombinant CHO-K1 cell line expressing the human voltage-gated potassium channel Kv3.1 (accession number NM_004976; Shaw-related subfamily, member1, KCN1).

    Additional Resource :  CYL3043091114 Datasheet

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    Contents: 2 x 1 mL aliquots containing 2.66 x 106 cells/mL in 7.5% DMSO at passage 8.
    Storage: Vials are to be stored in liquid N2.
    GMO: This product contains genetically modified organisms.
    Reference 1: 1. Ahn, H. S., Choi, J. S., Choi, B. H., Kim, M. J., Rhie, D. J., Yoon, S. H., Jo, Y. H.,Kim, M. S., Sung, K. W. and Hahn, S. J. (2005). Inhibition of the cloned delayed rectifier K+ channels, Kv1.5 and Kv3.1, by riluzole. Neuroscience 133(4), 1007-1
    Reference 2: 2. Friederich, P., Dilger, J. P., Isbrandt, D., Sauter, K., Pongs, O. and Urban, B. W. (2003). Biophysical properties of Kv3.1 channels in SH-SY5Y human neuroblastoma cells. Receptors Channels 9(6), 387-396.
    Reference 3: 3. Gan, L. and Kaczmarek, L. K. (1998). When, where, and how much Expression of the Kv3.1 potassium channel in high-frequency firing neurons J Neurobiol 37(1), 69-79.
    Reference 4: 4. Grissmer, S., Nguyen, A. N., Aiyar, J., Hanson, D. C., Mather, R. J., Gutman, G. A., Karmilowicz, M. J., Auperin, D. D. and Chandy, K. G. (1994). Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3,1.5,
    Reference 5: 5. Jarolimek, W., Soman, K. V., Alam, M. and Brown, A. M. (1996). Structureactivity relationship of quaternary ammonium ions at the external tetraethylammonium binding site of cloned potassium channels. Mol Pharmacol49(1), 165-171.
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