Glucosamine (N-acetyl)-6-Sulfatase/GNS Overexpression Lysate (Denatured)

Images

 
GNS transfected lysate.
Lane 1: GNS transfected lysate (60.83 KDa) Lane 2: Non-transfected lysate.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB

Order Details

Glucosamine (N-acetyl)-6-Sulfatase/GNS Overexpression Lysate (Denatured) Summary

Description
Pasmid: pCMV-GNS full-length
Gene
GNS

Packaging, Storage & Formulations

Storage
Store at -80C. Avoid freeze-thaw cycles.
Buffer
Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, and 0.01% Bromophenol blue).

Lysate Details for Glucosamine (N-acetyl)-6-Sulfatase/GNS

Type
Overexpression
Protein State
Denatured

Notes

Quality control test: Transient overexpression cell lysate was tested with Anti-GNS antibody by Western Blots.

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for Glucosamine (N-acetyl)-6-Sulfatase/GNS Overexpression Lysate (Denatured)

  • 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. Lysates are guaranteed for 6 months from date of receipt.

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Bioinformatics

Gene Symbol GNS
Entrez