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N-Sulfoglucosamine Sulfohydrolase (SGSH) ELISA Kits

SGSH encodes one of several enzymes involved in the lysosomal degradation of heparan sulfate. Additionally we are shipping SGSH Antibodies (60) and SGSH Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
SGSH 6448 P51688
Anti-Rat SGSH SGSH 688293  
SGSH 27029  
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Top SGSH ELISA Kits at antibodies-online.com

Showing 2 out of 7 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.054 ng/mL 0.15-10 ng/mL 96 Tests Log in to see 9 to 11 Days
$736.84
Details
Mouse 0.053 ng/mL 0.15-10 ng/mL 96 Tests Log in to see 9 to 11 Days
$757.89
Details

More ELISA Kits for SGSH Interaction Partners

Human N-Sulfoglucosamine Sulfohydrolase (SGSH) interaction partners

  1. results demonstrate that a single systemic scAAVrh74-hSGSH delivery mediated efficient restoration of SGSH activity and resulted in a near complete correction of MPS IIIA molecular pathology

  2. The crystal structure of glycosylated sulfamidase provides insight into the diverse effects of pathogenic mutations on sulfamidase function in mucopolysaccharidosis type IIIA.

  3. Pre-symptomatic treatment of progressive neurodegenerative disease (mucopolysaccharidosis type IIIA) via intra-cerebrospinal fluid injection of recombinant human SGSH mediates highly significant reductions in neuropathology in a canine model.

  4. Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications

  5. Sanfilippo syndrome (subtypes A and B) in Turkey: identification of novel mutations in SGSH and NAGLU (show NAGLU ELISA Kits)

  6. By assessing the degree of developmental regression over time a group of 7 pts (show PTS ELISA Kits) with a slowly progressive course of MPSIIIA were identified. In these 7 pts (show PTS ELISA Kits) and in 3 other mildly affected pts (show PTS ELISA Kits) missense mutation c.892T>C (p.Ser298Pro) was found on 1 allele

SGSH Antigen Profile

Antigen Summary

This gene encodes one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.

Gene names and symbols associated with SGSH

  • N-sulfoglucosamine sulfohydrolase (SGSH) antibody
  • N-sulfoglucosamine sulfohydrolase (Sgsh) antibody
  • N-sulfoglucosamine sulfohydrolase (sulfamidase) (Sgsh) antibody
  • 4632406A19Rik antibody
  • HSS antibody
  • MPS3A antibody
  • SFMD antibody

Protein level used designations for SGSH

N-sulphoglucosamine sulphohydrolase , heparan sulfate sulfatase , mucopolysaccharidosis type IIIA , sulfoglucosamine sulfamidase , sulphamidase , N-sulfoglucosamine sulfohydrolase

GENE ID SPECIES
6448 Homo sapiens
688293 Rattus norvegicus
27029 Mus musculus
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