Phospholipase D4 蛋白
(Phospholipase D4 (PLD4))
PLD4 (Phospholipase D Family Member 4) is a Protein Coding gene. Diseases associated with PLD4 include Nephrotic Syndrome, Type 7 and Doyne Honeycomb Retinal Dystrophy. Among its related pathways are Acyl chain remodelling of PE and Glycerophospholipid biosynthesis. Gene Ontology (GO) annotations related to this gene include phosphatidylinositol phospholipase C activity and N-acylphosphatidylethanolamine-specific phospholipase D activity. An important paralog of this gene is PLD3.
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9 results
PLD4
宿主: 人
宿主: HEK-293 Cells
Recombinant
The purity of the protein is greater than 95 % as determined by SDS-PAGE and Coomassie blue staining.
AM, ADA, IA, ScA
custom-made
PLD4
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).
SDS, ELISA, WB
custom-made
PLD4
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).
SDS, ELISA, WB
Aliases for Phospholipase D4 蛋白
phospholipase D family member 4 (PLD4) 蛋白phospholipase D family, member 4 (Pld4) 蛋白
AI132321 蛋白
C14orf175 蛋白
thss 蛋白
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