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- accession：NM_001145288
- 基因别名：SLC17A8
- 基因描述：Homo sapiens solute carrier family 17 (vesicular glutamate transporter), member 8 (SLC17A8), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：1620
- 翻译后氨基酸长度：539
- TranscriptVariant：This variant (2) lacks an exon in the coding region compared to variant 1. The encoded isoform (2) is shorter but has the same N- and C-termini compared to isoform 1.
- 基因简介：This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
- 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
