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Product Name
GALNS antibody
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Description
GALNS Rabbit Polyclonal antibody. Positive IHC detected in human kidney tissue. Positive WB detected in human liver tissue. Observed molecular weight by Western-blot: 50-55kd
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Tested applications
ELISA, WB, IHC
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Species reactivity
Human,Mouse,Rat; other species not tested.
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Alternative names
Chondroitinase antibody; Chondroitinsulfatase antibody; FLJ17434 antibody; FLJ42844 antibody; FLJ98217 antibody; Galactose 6 sulfate sulfatase antibody; GALNAC6S antibody; GalNAc6S sulfatase antibody; GALNS antibody; GAS antibody; MPS4A antibody
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Isotype
Rabbit IgG
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Preparation
This antibody was obtained by immunization of GALNS recombinant protein (Accession Number: NM_000512). Purification method: Antigen affinity purified.
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Clonality
Polyclonal
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Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:200-1:1000
IHC: 1:20-1:200
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Validations
human liver tissue were subjected to SDS PAGE followed by western blot with Catalog No:110845(GALNS antibody) at dilution of 1:400
Immunohistochemical of paraffin-embedded human kidney using Catalog No:110845(GALNS antibody) at dilution of 1:50 (under 10x lens)
Immunohistochemical of paraffin-embedded human kidney using Catalog No:110845(GALNS antibody) at dilution of 1:50 (under 40x lens)
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Background
GALNS(N-acetylgalactosamine-6-sulfatase) is also named as chondroitinase and belongs to the sulfatase family. It is one of sulfatases required to degrade glycosaminoglycans (GAGs), keratan sulfate (KS) and chondroitin-6-sulfate (C6S) and the enzyme is a dimer derived from two 60 kDa polypeptides, each of which is processed to 40 kDa and 15 kDa polypeptide subunits linked by disulfide bonds(PMID:15241807). The deduced 522-residue protein is composed of a 26-amino acid N-terminal signal peptide and a mature polypeptide of 496 amino acid residues, including 2 potential asparagine-linked glycosylation sites(PMID:1755850). Defects in GALNS are the cause of mucopolysaccharidosis type 4A (MPS4A), also known as Morquio A syndrome.
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