ARSB Mouse Monoclonal Antibody [Kloon ID: LBI4G7]

Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2016]

Carrier-free (BSA/glycerol-free) ARSB mouse monoclonal antibody, clone LBI4G7

ASB; G4S; MPS6

Homo sapiens arylsulfatase B (ARSB), transcript variant 1, mRNA.

411

P15848

Unconjugated

Glycosaminoglycan degradation, Lysosome, Metabolic pathways

Glycosaminoglycan degradation, Lysosome, Metabolic pathways

WB 1:500

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

ARSB

https://www.ncbi.nlm.nih.gov/gene/?term=411

https://www.uniprot.org/uniprot/P15848