ALMS1 encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein(ALMS1, centrosome and basal body associated protein) functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations ALMS1 cause Alstrom syndrome. There is a pseudogene for ALMS1 located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined. 蛋白別名為：ALMS1; KIAA0328; Alstrom syndrome protein 1;基因ID為：7840；蛋白質ID:Q8TCU4
應用類型
WB，IHC-p，ELISA補充：最優的抗體稀釋比例需要基于客戶實驗進行優化.建議的起始稀釋比例如下: WB: 1:500-1:2000, IHC-p: 1:100-1:300, ELISA: 1:40000. Not yet tested in other applications.
免疫原
合成多肽：the Internal region of human ALMS1. at AA rangle: 1530-1610
