iPLA2_ Polyclonal Antibody

Category: Antibodies
Catalog
E-AB-31820
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Product Name iPLA2_ Polyclonal Antibody
Description This gene encodes a member of the patatin-like phospholipase domain containing protein family. Members of this family are phospholipases which catalyze the cleavage of fatty acids from membrane phospholipids. The product of this gene is a calcium-independent phospholipase. Mutations in this gene have been associated with mitochondrial myopathy with lactic acidosis. Multiple transcript variants encoding different isoforms have been found for this gene.PNPLA8 (Patatin Like Phospholipase Domain Containing 8) is a Protein Coding gene. Diseases associated with PNPLA8 include Mitochondrial Myopathy With Lactic Acidosis and Weaver Syndrome. Among its related pathways are Acyl chain remodelling of PE and Eicosanoid Synthesis. GO annotations related to this gene include binding and calcium-independent phospholipase A2 activity. An important paralog of this gene is PLA2G6.
Synonyms PNPLA8, IPLA22, IPLA2G, BM-043, Calcium-independent phospholipase A2-gamma, Intracellular membrane-associated calcium-independent phospholipase A2 gamma, iPLA2-gamma, PNPLA-gamma, Patatin-like phospholipase domain-containing protein 8, iPLA
Host Rabbit
Immunogen Synthesized peptide derived from the C-terminal region of human iPLA2_
Isotype IgG
Reactivity Human, Mouse
Applications ELISA, WB
Form PBS with 0.02% sodium azide, 0.5% BSA and 50% glycerol, pH7.4
Uniprot Q9NP80
Background This gene encodes a member of the patatin-like phospholipase domain containing protein family. Members of this family are phospholipases which catalyze the cleavage of fatty acids from membrane phospholipids. The product of this gene is a calcium-independent phospholipase. Mutations in this gene have been associated with mitochondrial myopathy with lactic acidosis. Multiple transcript variants encoding different isoforms have been found for this gene.PNPLA8 (Patatin Like Phospholipase Domain Containing 8) is a Protein Coding gene. Diseases associated with PNPLA8 include Mitochondrial Myopathy With Lactic Acidosis and Weaver Syndrome. Among its related pathways are Acyl chain remodelling of PE and Eicosanoid Synthesis. GO annotations related to this gene include binding and calcium-independent phospholipase A2 activity. An important paralog of this gene is PLA2G6.
Supplier Elabscience

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