LCA5 蛋白
(Leber Congenital Amaurosis 5 (LCA5))
This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009].
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4 results
custom-made
LCA5
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
LCA5
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, WB, SDS
LCA5
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
Greater than 90 % as determined by SDS-PAGE.
ELISA, WB
Aliases for LCA5 蛋白
LCA5, lebercilin (LCA5) 蛋白Leber congenital amaurosis 5 (LOC787523) 蛋白
LCA5, lebercilin (Lca5) 蛋白
Leber congenital amaurosis 5 (human) (Lca5) 蛋白
4930431B11Rik 蛋白
5730406O13Rik 蛋白
AV274874 蛋白
C6orf152 蛋白
ORF64 蛋白
RGD1308555 蛋白
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