服务热线：
- 商品货号：G123612
- accession：NM_206883
- 基因别名：SLC26A5
- 基因描述：Homo sapiens solute carrier family 26 (anion exchanger), member 5 (SLC26A5), transcript variant b, mRNA.
- 载体：现货载体
- CDS区长度：2058
- 翻译后氨基酸长度：685
- TranscriptVariant：This variant (b), also known as SLC26A5b, uses an alternate 3' end-exon compared to variant a. The resulting isoform (b) has a distinct and shorter C-terminus, as compared to isoform a.
- 基因简介：This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]
- 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
服务时间：24小时在线客服
客服热线：400-000-7085
丰晖生物
中国优质生物资源平台
在线客服