PLEKHM1 蛋白
(Pleckstrin Homology Domain Containing, Family M (With RUN Domain) Member 1 (PLEKHM1))
The protein encoded by this gene is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Mutations in this gene are associated with autosomal recessive osteopetrosis type 6 (OPTB6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009].
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5 results
custom-made
PLEKHM1
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, SDS, WB
custom-made
PLEKHM1
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
PLEKHM1
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 PLEKHM1 蛋白
pleckstrin homology and RUN domain containing M1 (PLEKHM1) 蛋白pleckstrin homology domain containing, family M (with RUN domain) member 1 (PLEKHM1) 蛋白
pleckstrin homology domain containing, family M (with RUN domain) member 1 (Plekhm1) 蛋白
pleckstrin homology and RUN domain containing M1 (Plekhm1) 蛋白
AP162 蛋白
B2 蛋白
BC038943 蛋白
D330036J23Rik 蛋白
OPTB6 蛋白
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