OCRL 蛋白
(Oculocerebrorenal Syndrome of Lowe (OCRL))
This gene encodes a phosphatase enzyme that is involved in actin polymerization and is found in the trans-Golgi network. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. [provided by RefSeq, Jul 2008].
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custom-made
OCRL
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
OCRL
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
Aliases for OCRL 蛋白
OCRL, inositol polyphosphate-5-phosphatase (Ocrl) 蛋白phosphatidylinositol polyphosphate 5-phosphatase (NAEGRDRAFT_58601) 蛋白
OCRL, inositol polyphosphate-5-phosphatase (OCRL) 蛋白
oculocerebrorenal syndrome of Lowe (ocrl) 蛋白
OCRL, inositol polyphosphate-5-phosphatase (ocrl) 蛋白
9530014D17Rik 蛋白
BB143339 蛋白
inpp5f 蛋白
INPP5F 蛋白
locr 蛋白
LOCR 蛋白
nphl2 蛋白
NPHL2 蛋白
OCRL 蛋白
OCRL-1 蛋白
ocrl1 蛋白
OCRL1 蛋白
wu:fi09g03 蛋白
zgc:152864 蛋白
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