ACADS polyclonal, anti-human, mouse, rat
€295.00
In stock
SKU
K008274P
Catalog Number: K008274P
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB, IHC
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Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB, IHC
Request Manual
Questions? Contact us!
Background:
This gene encodes a a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with Short Chain Acyl-CoA Dehydrogenase Deficiency. It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.
Synonyms: SCAD, ACAD3
Cellular Location: Cytoplasm
Immunogen:
Recombinant protein of human ACADS
Gene Symbol: ACADS
Gene ID: 35
Swiss prot: P16219
Calculated MW: 44kDa
Recommended dilution:
WB 1:200-1000, IHC 1:25-100,
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
This gene encodes a a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with Short Chain Acyl-CoA Dehydrogenase Deficiency. It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.
Synonyms: SCAD, ACAD3
Cellular Location: Cytoplasm
Immunogen:
Recombinant protein of human ACADS
Gene Symbol: ACADS
Gene ID: 35
Swiss prot: P16219
Calculated MW: 44kDa
Recommended dilution:
WB 1:200-1000, IHC 1:25-100,
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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