- accession:NM_001012227
- 基因别名:Xk
- 基因描述:Rattus norvegicus X-linked Kx blood group (McLeod syndrome) (Xk), mRNA.
- 载体:现货载体
- CDS区长度:1338
- 翻译后氨基酸长度:445
- 基因简介:human homolog is a red cell membrane protein whose deficiency causes the McLeod syndrome, a disorder characterized by blood group, neuromuscular and hematopoietic abnormalities [RGD, Feb 2006]
- 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