FAM161A 蛋白
(Family with Sequence Similarity 161, Member A (FAM161A))
This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011].
Recommended next Filters:
您想试用我们的人工智能搜索吗？
4 results :
custom-made
FAM161A
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
custom-made
FAM161A
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, SDS, WB
FAM161A
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for FAM161A 蛋白
family with sequence similarity 161 member A (FAM161A) 蛋白family with sequence similarity 161, member A (Fam161a) 蛋白
family with sequence similarity 161, member A (FAM161A) 蛋白
4930430E16Rik 蛋白
RGD1304999 蛋白
RP28 蛋白
您还需要查找其他产品吗？
You are here:
