NEU1 polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS8111
Background:
NEU1 encodes the lysosomal enzyme neuraminidase, Neu1, which cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids . In the lysosome Neu1 belongs to a heterotrimeric complex containing beta-galactosidase and cathepsin A (also referred to as 'protective protein') . In humans, primary or secondary deficiency of this enzyme leads to two clinically similar neurodegenerative lysosomal storage disorders: sialidosis and galactosialidosis (GS) . Sialidosis symptoms range from eye abnormalities and neurological disturbances to skeletal malformations, mental retardation and early death. Neu1 is expressed in the pancreas, muscle, kidney, placenta, heart, lung and liver. The human Neu1 gene maps to chromosome 6p21.33 and encodes a lysosomal protein localized on the inner side of the plasma membrane and in intracellular vesicles . Neu1 is also known as alpha-N-acetyl-neuraminidase and Acetylneuraminyl hydrolase .
Alternative Name:
Sialidase-1, Acetylneuraminyl hydrolase, G9 sialidase, Lysosomal sialidase, N-acetyl-alpha-neuraminidase 1, NEU1, NANH
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: NEU1 polyclonal antibody detects endogenous levels of NEU1 protein.
Immunogen:
Recombinant full length Human NEU1.
MW: ~ 45 kDa
Swis Prot.: Q99519
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
NEU1 encodes the lysosomal enzyme neuraminidase, Neu1, which cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids . In the lysosome Neu1 belongs to a heterotrimeric complex containing beta-galactosidase and cathepsin A (also referred to as 'protective protein') . In humans, primary or secondary deficiency of this enzyme leads to two clinically similar neurodegenerative lysosomal storage disorders: sialidosis and galactosialidosis (GS) . Sialidosis symptoms range from eye abnormalities and neurological disturbances to skeletal malformations, mental retardation and early death. Neu1 is expressed in the pancreas, muscle, kidney, placenta, heart, lung and liver. The human Neu1 gene maps to chromosome 6p21.33 and encodes a lysosomal protein localized on the inner side of the plasma membrane and in intracellular vesicles . Neu1 is also known as alpha-N-acetyl-neuraminidase and Acetylneuraminyl hydrolase .
Alternative Name:
Sialidase-1, Acetylneuraminyl hydrolase, G9 sialidase, Lysosomal sialidase, N-acetyl-alpha-neuraminidase 1, NEU1, NANH
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: NEU1 polyclonal antibody detects endogenous levels of NEU1 protein.
Immunogen:
Recombinant full length Human NEU1.
MW: ~ 45 kDa
Swis Prot.: Q99519
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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