SGSH Antibody

Code CSB-PA021200GA01HU
Size US$685
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Product Details

Uniprot No. P51688
Target Names SGSH
Alternative Names Heparan sulfate sulfatase antibody; Heparan sulphate sulphatase antibody; HSS antibody; MPS 3A antibody; MPS3 A antibody; MPS3A antibody; Mucopolysaccharidosis type IIIA antibody; N sulfoglucosamine sulfohydrolase (sulfamidase) antibody; N sulfoglucosamine sulfohydrolase antibody; N-sulphoglucosamine sulphohydrolase antibody; SFMD antibody; SGSH antibody; SPHM_HUMAN antibody; Sulfoglucosamine sulfamidase antibody; Sulphamidase antibody; Sulphoglucosamine sulphamidase antibody
Raised in Rabbit
Species Reactivity Human,Mouse,Rat
Immunogen Human SGSH
Immunogen Species Homo sapiens (Human)
Isotype IgG
Purification Method Antigen Affinity purified
Concentration It differs from different batches. Please contact us to confirm it.
Buffer PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Tested Applications ELISA,IHC
Protocols ELISA Protocol
Immunohistochemistry (IHC) Protocol
Troubleshooting and FAQs Antibody FAQs
Storage Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
(From Uniprot)
Catalyzes a step in lysosomal heparan sulfate degradation.
Gene References into Functions
  1. CSF enzyme activity levels for either SGSH (in MPS IIIA subjects) or NAGLU (in MPS IIIB) significantly differed from normal controls. Several other behavioral or functional measures were found to be uninformative in this population, including timed functional motor tests. PMID: 27590925
  2. We have identified ocular features of a patient with Sanfilippo syndrome type IIIA harboring a novel SGHS mutation that were not previously known to occur in this disease - namely, a progressive retinopathy with distinctive features, cystic macular changes responsive to carbonic anhydrase inhibitors, and complex electroretinographic abnormalities consistent with postreceptoral dysfunction. PMID: 26331342
  3. 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 PMID: 25592334
  4. The crystal structure of glycosylated sulfamidase provides insight into the diverse effects of pathogenic mutations on sulfamidase function in mucopolysaccharidosis type IIIA. PMID: 24816101
  5. 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. PMID: 21550404
  6. Processing and secretion of p.Ser298Pro sulfamidase suggests that small amounts of the newly synthesized enzyme are transported to lysosomes PMID: 21671382
  7. Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications PMID: 11668611
  8. Sanfilippo syndrome (subtypes A and B) in Turkey: identification of novel mutations in SGSH and NAGLU PMID: 11793481
  9. expression studies of four novel mutations PMID: 15146460
  10. analysis of a nonsense mutation (Y40X) and two de novo missense mutations (E300V; Q307P) in heparan N-sulphatase in a mucopolysaccharidosis IIIA patient [case report] PMID: 15902564
  11. By assessing the degree of developmental regression over time a group of 7 pts with a slowly progressive course of MPSIIIA were identified. In these 7 pts and in 3 other mildly affected pts missense mutation c.892T>C (p.Ser298Pro) was found on 1 allele PMID: 18407553

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Involvement in disease Mucopolysaccharidosis 3A (MPS3A)
Subcellular Location Lysosome
Protein Families Sulfatase family
Database Links

HGNC: 10818

OMIM: 252900

KEGG: hsa:6448

STRING: 9606.ENSP00000314606

UniGene: Hs.31074

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