Western Blot: Glucosamine (N-acetyl)-6-Sulfatase/GNS Antibody (007) [NBP2-89413] - Lane A: PC3 Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 ...read more
Glucosamine (N-acetyl)-6-Sulfatase/GNS Antibody (007) - Azide and BSA Free Summary
Description
This antibody can be stored at 2C-8C for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20C to -80C. Avoid repeated freeze-thaw cycles.
Additional Information
Recombinant Monoclonal Antibody
Immunogen
This antibody was obtained from a rabbit immunized with purified, recombinant Human Glucosamine (N-acetyl)-6-Sulfatase/GNS (Accession#: NP_002067.1; Met 1-Leu 552).
Source
HEK293
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Gene
GNS
Purity
Protein A purified
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Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
0.2 um filtered solution in PBS
Preservative
No Preservative
Purity
Protein A purified
Alternate Names for Glucosamine (N-acetyl)-6-Sulfatase/GNS Antibody (007) - Azide and BSA Free
EC 3.1.6
EC 3.1.6.14
G6Sglucosamine-6-sulfatase
glucosamine (N-acetyl)-6-sulfatase
Glucosamine6Sulfatase
Glucosamine-6-Sulfatase
GNS
MGC21274
N-acetylglucosamine-6-sulfatase
Background
The product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome. [provided by RefSeq]
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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