蛋白质/抗原/多肽 >> 重组蛋白
重组选择连接蛋白32
产品介绍 基因名: Snx32 产品别名: B930037P14Rik; Snx6b; Snx32; sorting nexin 32; sorting nexin 32; sorting nexin-32; sortin nexin-6B; sorting nexin-6B; 选择连接蛋白32; 背景信息: SNX32 is a 403 amino acid protein that contains one PX (phox homology) domain and belongs to the sorting nexin family. Existing as two alternatively spliced isoforms, SNX32 may be involved in several stages of intracellular trafficking. The gene that encodes SNX32 consists of approximately 23,256 bases and maps to human chromosome 11q13.1. Housing over 1,400 genes and comprising nearly 4% of the human genome, chromosome 11 is considered a gene and disease association-dense chromosome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that map to chromosome 11. In addition, the blood disorders Sickle cell anemia and thalassemia are caused by mutations in the HBB gene, which is located on chromosome 11. 标签:His-tag |
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