| 货号 | APC-017-25ul |
| 描述 | Each antibody ordered from Alomone Labs is supplied with its corresponding control peptide (antigen), free of charge. A Rabbit Polyclonal antibody to KV4.3 Channel |
| 反应种属 | H, M, R |
| 应用 | IC, IH, IP, WB |
| 供应商 | Alomone |
| 背景 | Kv4.3 is a voltage-dependent K+ channel that belongs to the Shal channel subfamily and includes two other members: Kv4.1 and Kv4.2. Kv4.3 possesses the signature structure of the voltage-dependent K+ channels: six membrane-spanning domains with intracellular N and C termini. As with other members of the voltage-gated K+ channel superfamily, the functional channel is a tetramer that can be composed of more than one member of the Shal subfamily, i.e. heterotetramers of Kv4.1 and Kv4.2. The Kv4 channels are characterized by activation at subthreshold membrane potentials, inactivate rapidly and recover from inactivation quickly compared with other voltage-dependent K+ channels. This type of current is known as transient A-type K+ currents.1 The biophysical properties of the Kv4.3 subunit can be modified by its association with auxiliary β subunits such as the KChIP family that increase current densities and accelerates both the inactivation and the recovery time. Kv4.3 is highly expressed in the brain where it has a key role in shaping the action potential and firing frequency of neurons. In the heart together with Kv4.2 it underlies the fast inactivating and recovering cardiac transient outward current Ito.2,3 The channel is also expressed in smooth muscle cells of several organs such as myometrium, lung and colon where its function has not been completely elucidated. Several toxins from spider venoms are potent blockers (affecting the channels in the nanomolar range) of KV4.3 channels. Among these the most potent and selective are Phrixotoxin-1 (#STP-700) (28 nM) and Phrixotoxin-2 (#P-700), (71 nM). 4 |
| 运输条件 | Ambient |
| 存放说明 | -20 |
| 纯度 | Affinity purified on immobilized antigen. |
| 参考文献 | 1.Serodio, P.et al. (1994)J. Neurophysiol.72,1516. 2.Tsaur, M.L.et al. (1997)FEBS Lett.400,215. 3.Guo, W.et al. (2002)Circ. Res.90,586. 4.Diochot, S. et al. (1999) Br. J. Pharmacol. 126, 251. |
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