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Human Monoclonal HS6ST1 Primary Antibody for ELISA, WB - ABIN522851
Lu, Auduong, White, Yue: Up-regulation of heparan sulfate 6-O-sulfation in idiopathic pulmonary fibrosis. in American journal of respiratory cell and molecular biology 2014
Distinct expression patterns of Sulf1 (show SULF1 Antibodies) and Hs6st1 spatially regulate heparan sulfate sulfation during prostate development.
both HS6ST-1 and HS6ST-2 (show HS6ST2 Antibodies) are involved in 6-O-sulfation of heparin and that the proper packaging and storage of tryptase (show TPSAB1 Antibodies)
6OST1 is predominantly transcribed in epithelial and neural-derived tissues during development
Data show that high expression of 6-O-sulfotransferase (6-OST)-1, 2, or 3 resulted in increased 6-O-sulfation of N-sulfated (show SULF1 Antibodies) and N-acetylated glucosamine units, and in altered heparan sulfate domain structure.
Hs2st and/or Hs6st1 expression coincides with Slit expression domains at locations where retinal ganglion cell(RGC) axons make navigation errors in Hs2st-/- and Hs6st1-/- mutants, and Hs6st1-/-RGC axons are less sensitive to Slit2 repulsion.
there is a critical role for HS 6-O sulfation by Hs6st1 in postnatal processes
HS6ST-1 and HS6ST-2 (show HS6ST2 Antibodies) have roles in regulating the angiogenic program in ovarian cancer cells affecting HB-EGF (show HBEGF Antibodies) signaling and subsequent expression of angiogenic cytokines by cancer cells
Hs6st1 and Hs2st (show HS2ST1 Antibodies) generate conditions conducive to corpus callosum development.
idiopathic hypogonadotrophic hypogonadism--associated HS6ST1 mutations display reduced activity in vitro and in vivo, suggesting that HS6ST1 and the complex modifications of extracellular sugars are critical for normal development
we have characterized HS6ST-2 (show HS6ST2 Antibodies) and HS6ST-1 human isologues, including their chromosomal localizations,HS6STs could also transfer sulphate to N -sulphoglucosamine residues located at the non-reducing terminal of HS with high affinity.
The protein encoded by this gene is a member of the heparan sulfate biosynthetic enzyme family. Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biological activities. This enzyme is a type II integral membrane protein and is responsible for 6-O-sulfation of heparan sulfate. This enzyme does not share significant sequence similarity with other known sulfotransferases. A pseudogene located on chromosome 1 has been found for this gene.
, heparan-sulfate 6-O-sulfotransferase 1
, heparan-sulfate 6-sulfotransferase
, Heparan-sulfate 6-O-sulfotransferase 1
, heparan sulfate 6-sulfotransferase