Recombinant Glucosamine (N-acetyl) -6-Sulfatase/G6S Monoclonaal antilichaam

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.

GNS

P15586

Human

Recombinant Human GNS protein

GNS; G6S; Glucosamine-6-Sulfatase; N-Acetylglucosamine-6-Sulfatase

4D5

Unconjugated

WB

Tags & Cell Markers; Signal Transduction; Cell Biology; Metabolism

Protein A

1 mg/mL

WB 1:500-1:2000

0.2 μm filtered solution in PBS

Ice bag

This antibody can be stored at 2°C-8°C for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20°C to -80°C. Preservative-Free. Avoid repeated freeze-thaw cycles.

https://789.bio/eb/g6amDTwb

62 kDa

95 kDa

IgG