catalog number :
MBS710510
products full name :
Rabbit anti-human N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 polyclonal Antibody
products short name :
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
products name syn :
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1; NDST1; HSST; NST1
other names :
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1, isoform CRA_a; Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1; bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1; NDST-1; HSNST 1; N-HSST 1; N-heparan sulfate sulfotransferase 1; glucosaminyl N-deacetylase/N-sulfotransferase 1; heparan sulfate-N-deacetylase/N-sulfotransferase; [Heparan sulfate]-glucosamine N-sulfotransferase 1; N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1; Glucosaminyl N-deacetylase/N-sulfotransferase 1; NDST-1; N-heparan sulfate sulfotransferase 1; N-HSST 1; [Heparan sulfate]-glucosamine N-sulfotransferase 1; HSNST 1
other gene names :
NDST1; NDST1; HSST; NST1; HSST; HSST1; NDST-1; N-HSST 1; HSNST 1
uniprot entry name :
NDST1_HUMAN
reactivity :
Human, Mouse, Rat
purity :
Antigen Affinity Purified
tested application :
ELISA (EIA), Immunohistochemistry (IHC)
other info1 :
Immunogen: Human NDST1
other info2 :
Storage Buffer: PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20 degree C, Avoid freeze / thaw cycles.
ncbi acc num :
EAW61720.1
ncbi mol weight :
62,065 Da
ncbi pathways :
Disease Pathway (530764); Glycogen Storage Diseases Pathway (980468); Glycosaminoglycan Biosynthesis - Heparan Sulfate / Heparin Pathway (82984); Glycosaminoglycan Biosynthesis - Heparan Sulfate / Heparin Pathway (358); Glycosaminoglycan Biosynthesis, Heparan Sulfate Backbone Pathway (413365); Glycosaminoglycan Biosynthesis, Heparan Sulfate Backbone Pathway (468252); Glycosaminoglycan Metabolism Pathway (645297); HS-GAG Biosynthesis Pathway (645306); Heparan Sulfate/heparin (HS-GAG) Metabolism Pathway (645304); MPS I - Hurler Syndrome Pathway (685537)
ncbi summary :
This gene encodes a member of the heparan sulfate/heparin GlcNAc N-deacetylase/ N-sulfotransferase family. The encoded enzyme is a type II transmembrane protein that resides in the Golgi apparatus. The encoded protein catalyzes the transfer of sulfate from 3'-phosphoadenosine 5'-phosphosulfate to nitrogen of glucosamine in heparan sulfate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
uniprot summary :
NDST1: Essential bifunctional enzyme that catalyzes both the N- deacetylation and the N-sulfation of glucosamine (GlcNAc) of the glycosaminoglycan in heparan sulfate. Modifies the GlcNAc-GlcA disaccharide repeating sugar backbone to make N-sulfated heparosan, a prerequisite substrate for later modifications in heparin biosynthesis. Plays a role in determining the extent and pattern of sulfation of heparan sulfate. Compared to other NDST enzymes, its presence is absolutely required. Participates in biosynthesis of heparan sulfate that can ultimately serve as L- selectin ligands, thereby playing a role in inflammatory response. Belongs to the sulfotransferase 1 family. NDST subfamily. 2 isoforms of the human protein are produced by alternative splicing. Protein type: Membrane protein, integral; Transferase; Glycan Metabolism - heparan sulfate biosynthesis; Hydrolase; EC 2.8.2.8. Chromosomal Location of Human Ortholog: 5q33.1. Cellular Component: Golgi membrane; integral to membrane. Molecular Function: deacetylase activity; [heparan sulfate]-glucosamine N-sulfotransferase activity. Biological Process: smoothened signaling pathway; fibroblast growth factor receptor signaling pathway; glycosaminoglycan metabolic process; MAPKKK cascade; pathogenesis; respiratory gaseous exchange; embryonic viscerocranium morphogenesis; polysaccharide biosynthetic process; glycosaminoglycan biosynthetic process; heparin biosynthetic process; forebrain development; midbrain development; heparan sulfate proteoglycan biosynthetic process; carbohydrate metabolic process; embryonic neurocranium morphogenesis; inflammatory response. Disease: Mental Retardation, Autosomal Recessive 46