×
![]()
- accession：NM_020822
- 基因别名：KCNT1
- 基因描述：Homo sapiens potassium channel, subfamily T, member 1 (KCNT1), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：3708
- 翻译后氨基酸长度：1235
- TranscriptVariant：This variant (1) encodes the longer isoform (1).
- 基因简介：Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
