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Carbohydrate sulfotransferase

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Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of galactose (Gal) residues of keratan. Has a preference for sulfating keratan sulfate, but it also transfers sulfate to the unsulfated polymer. The sulfotransferase activity on sialyl LacNAc structures is much higher than the corresponding desialylated substrate, and only internal Gal residues are sulfated. May function in the sulfation of sialyl N-acetyllactosamine oligosaccharide chains attached to glycoproteins. Participates in biosynthesis of selectin ligands. Selectin ligands are present in high endothelial cells (HEVs) and play a central role in lymphocyte homing at sites of inflammation.

Below are the list of possible Carbohydrate sulfotransferase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Carbohydrate sulfotransferase 1

 Carbohydrate sulfotransferase 1 ELISA Kit
 Carbohydrate sulfotransferase 1 Recombinant
 Carbohydrate sulfotransferase 1 Antibody
Also known as Carbohydrate sulfotransferase 1 (Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 1) (GST-1) (Keratan sulfate Gal-6 sulfotransferase) (KS6ST) (KSGal6ST) (KSST).
CHST1: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of galactose (Gal) residues of keratan. Has a preferenc
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e for sulfating keratan sulfate, but it also transfers sulfate to the unsulfated polymer. The sulfotransferase activity on sialyl LacNAc structures is much higher than the corresponding desialylated substrate, and only internal Gal residues are sulfated. May function in the sulfation of sialyl N- acetyllactosamine oligosaccharide chains attached to glycoproteins. Participates in biosynthesis of selectin ligands. Selectin ligands are present in high endothelial cells (HEVs) and play a central role in lymphocyte homing at sites of inflammation. Belongs to the sulfotransferase 1 family. Gal/GlcNAc/GalNAc subfamily.

Protein type: EC 2.8.2.21; Glycan Metabolism - keratan sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 11p11.2

Cellular Component: Golgi membrane

Molecular Function: keratan sulfotransferase activity; N-acetylglucosamine 6-O-sulfotransferase activity; sulfotransferase activity

Biological Process: galactose metabolic process; keratan sulfate biosynthetic process; keratan sulfate metabolic process; polysaccharide metabolic process; sulfur metabolic process
 CHST1 ELISA Kit
 CHST1 Recombinant
 CHST1 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 10

 Carbohydrate sulfotransferase 10 ELISA Kit
 Carbohydrate sulfotransferase 10 Recombinant
 Carbohydrate sulfotransferase 10 Antibody
Also known as Carbohydrate sulfotransferase 10 (HNK-1 sulfotransferase) (HNK-1ST) (HNK1ST).
Catalyzes the transfer of sulfate to position 3 of terminal glucuronic acid of both protein- and lipid-linked oligosaccharides. Participates in biosynthesis of HNK-1 carbohydrate structure, a sulfated glucuronyl-lactosaminyl residue carried by many neural recognition molecules.
 chst10 ELISA Kit
 chst10 Recombinant
 chst10 Antibody
 zgc:100964 ELISA Kit
 zgc:100964 Recombinant
 zgc:100964 Antibody
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Carbohydrate sulfotransferase 11

 Carbohydrate sulfotransferase 11 ELISA Kit
 Carbohydrate sulfotransferase 11 Recombinant
 Carbohydrate sulfotransferase 11 Antibody
Also known as Carbohydrate sulfotransferase 11 (Chondroitin 4-O-sulfotransferase 1) (Chondroitin 4-sulfotransferase 1) (C4S-1) (C4ST-1) (C4ST1).
CHST11: Catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage and is distributed on the surfaces of many cells and
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extracellular matrices. Can also sulfate Gal residues in desulfated dermatan sulfate. Preferentially sulfates in GlcA->GalNAc unit than in IdoA->GalNAc unit. Does not form 4, 6- di-O-sulfated GalNAc when chondroitin sulfate C is used as an acceptor. A chromosomal aberration involving CHST11 is found in B-cell chronic lymphocytic leukemias. Translocation t(12;14)(q23;q32) with IgH. Belongs to the sulfotransferase 2 family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 2.8.2.5; Energy Metabolism - sulfur; Glycan Metabolism - chondroitin sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 12q

Cellular Component: Golgi membrane; membrane

Molecular Function: chondroitin 4-sulfotransferase activity; N-acetylgalactosamine 4-O-sulfotransferase activity

Biological Process: chondroitin sulfate biosynthetic process
 CHST11 ELISA Kit
 CHST11 Recombinant
 CHST11 Antibody
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Carbohydrate sulfotransferase 12

 Carbohydrate sulfotransferase 12 ELISA Kit
 Carbohydrate sulfotransferase 12 Recombinant
 Carbohydrate sulfotransferase 12 Antibody
Also known as Carbohydrate sulfotransferase 12 (Chondroitin 4-O-sulfotransferase 2) (Chondroitin 4-sulfotransferase 2) (C4ST-2) (C4ST2).
Catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of chondroitin and desulfated dermatan sulfate. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage and is distributed on the surfaces o
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f many cells and extracellular matrices ().
 chst12 ELISA Kit
 chst12 Recombinant
 chst12 Antibody
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Carbohydrate sulfotransferase 13

 Carbohydrate sulfotransferase 13 ELISA Kit
 Carbohydrate sulfotransferase 13 Recombinant
 Carbohydrate sulfotransferase 13 Antibody
Also known as Carbohydrate sulfotransferase 13 (Chondroitin 4-O-sulfotransferase 3) (Chondroitin 4-sulfotransferase 3) (C4ST-3) (C4ST3).
CHST13: Catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage and is distributed on the surfaces of many cells and extrace
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llular matrices. Transfers sulfate to the C4 hydroxyl of beta1,4-linked GalNAc that is substituted with a beta-linked glucuronic acid at the C-3 hydroxyl. No activity toward dermatan. Belongs to the sulfotransferase 2 family.

Protein type: EC 2.8.2.5; Energy Metabolism - sulfur; Glycan Metabolism - chondroitin sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 3q21.3

Cellular Component: Golgi membrane

Molecular Function: chondroitin 4-sulfotransferase activity; N-acetylgalactosamine 4-O-sulfotransferase activity

Biological Process: chondroitin sulfate biosynthetic process
 CHST13 ELISA Kit
 CHST13 Recombinant
 CHST13 Antibody
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Carbohydrate sulfotransferase 14

 Carbohydrate sulfotransferase 14 ELISA Kit
 Carbohydrate sulfotransferase 14 Recombinant
 Carbohydrate sulfotransferase 14 Antibody
Also known as Carbohydrate sulfotransferase 14 (Dermatan 4-sulfotransferase 1) (D4ST-1).
CHST14: Catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of dermatan sulfate. Plays a pivotal role in the formation of 4-0-sulfated IdoA blocks in dermatan sulfate. Transfers sulfate to the C-4 hydroxyl of beta1,4-linked GalNAc that is substituted with an alpha-l
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inked iduronic acid (IdoUA) at the C-3 hydroxyl. Transfers sulfate more efficiently to GalNAc residues in -IdoUA-GalNAc-IdoUA- than in -GlcUA-GalNAc-GlcUA-sequences. Has preference for partially desulfated dermatan sulfate. Addition of sulfate to GalNAc may occur immediately after epimerization of GlcUA to IdoUA. GlcUA to IdoUA. Appears to have an important role in the formation of the cerbellar neural network during postnatal brain development. Defects in CHST14 are the cause of Ehlers-Danlos syndrome musculocontractural type (EDSMC). It is a form of Ehlers-Danlos syndrome characterized by distinctive craniofacial dysmorphism, congenital contractures of thumbs and fingers, clubfeet, severe kyphoscoliosis, muscular hypotonia, hyperextensible thin skin with easy bruisability and atrophic scarring, wrinkled palms, joint hypermobility, and ocular involvement. Belongs to the sulfotransferase 2 family.

Protein type: EC 2.8.2.35; Glycan Metabolism - chondroitin sulfate biosynthesis; Membrane protein, integral; Transferase

Molecular Function: N-acetylgalactosamine 4-O-sulfotransferase activity; protein binding

Biological Process: dermatan sulfate biosynthetic process; dermatan sulfate proteoglycan metabolic process
 Chst14 ELISA Kit
 Chst14 Recombinant
 Chst14 Antibody
 D4st1 ELISA Kit
 D4st1 Recombinant
 D4st1 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 15

 Carbohydrate sulfotransferase 15 ELISA Kit
 Carbohydrate sulfotransferase 15 Recombinant
 Carbohydrate sulfotransferase 15 Antibody
Also known as Carbohydrate sulfotransferase 15 (B-cell RAG-associated gene protein) (hBRAG) (N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase) (GalNAc4S-6ST).
CHST15: Sulfotransferase that transfers sulfate from 3'- phosphoadenosine 5'-phosphosulfate (PAPS) to the C-6 hydroxyl group of the GalNAc 4-sulfate residue of chondroitin sulfate A and forms chondroitin sulfate E containing GlcA-GalNAc(4,6-SO(4)) repeating units. It also transfers sulfate to a unique non- reducing terminal sequence, GalNAc(4SO4)-GlcA(2SO4)-GalNAc(6SO4), to yield a highly sulfated structure similar to the structur
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e found in thrombomodulin chondroitin sulfate. May also act as a B- cell receptor involved in BCR ligation-mediated early activation that mediate regulatory signals key to B-cell development and/or regulation of B-cell-specific RAG expression; however such results are unclear in vivo. Belongs to the sulfotransferase 1 family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 2.8.2.33; Glycan Metabolism - chondroitin sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 10q26

Cellular Component: Golgi membrane

Molecular Function: 3'-phosphoadenosine 5'-phosphosulfate binding; N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase activity

Biological Process: chondroitin sulfate biosynthetic process; hexose biosynthetic process
 CHST15 ELISA Kit
 CHST15 Recombinant
 CHST15 Antibody
 BRAG ELISA Kit
 BRAG Recombinant
 BRAG Antibody
 GALNAC4S6ST ELISA Kit
 GALNAC4S6ST Recombinant
 GALNAC4S6ST Antibody
 KIAA0598 ELISA Kit
 KIAA0598 Recombinant
 KIAA0598 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 2

 Carbohydrate sulfotransferase 2 ELISA Kit
 Carbohydrate sulfotransferase 2 Recombinant
 Carbohydrate sulfotransferase 2 Antibody
Also known as Carbohydrate sulfotransferase 2 (Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 2) (GST-2) (N-acetylglucosamine 6-O-sulfotransferase 1) (GlcNAc6ST-1) (Gn6ST-1).
CHST2: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of non-reducing N-acetylglucosamine (GlcNAc) residues
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within keratan-like structures on N-linked glycans and within mucin-associated glycans that can ultimately serve as SELL ligands. SELL ligands are present in high endothelial cells (HEVs) and play a central role in lymphocyte homing at sites of inflammation. Participates in biosynthesis of the SELL ligand sialyl 6-sulfo Lewis X and in lymphocyte homing to Peyer patches. Has no activity toward O-linked sugars. Its substrate specificity may be influenced by its subcellular location. Sulfates GlcNAc residues at terminal, non-reducing ends of oligosaccharide chains. Belongs to the sulfotransferase 1 family. Gal/GlcNAc/GalNAc subfamily. 2 isoforms of the human protein are produced by alternative initiation.

Protein type: EC 2.8.2.-; Glycan Metabolism - keratan sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 3q24

Cellular Component: Golgi membrane; integral to membrane; trans-Golgi network

Molecular Function: N-acetylglucosamine 6-O-sulfotransferase activity; sulfotransferase activity

Biological Process: keratan sulfate biosynthetic process; multicellular organismal development; N-acetylglucosamine metabolic process; sulfur metabolic process
 CHST2 ELISA Kit
 CHST2 Recombinant
 CHST2 Antibody
 GN6ST ELISA Kit
 GN6ST Recombinant
 GN6ST Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 3

 Carbohydrate sulfotransferase 3 ELISA Kit
 Carbohydrate sulfotransferase 3 Recombinant
 Carbohydrate sulfotransferase 3 Antibody
Also known as Carbohydrate sulfotransferase 3 (Chondroitin 6-O-sulfotransferase 1) (C6ST-1).
Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of the N-acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage and is distributed on
>>>
the surfaces of many cells and extracellular matrices ().
 CHST3 ELISA Kit
 CHST3 Recombinant
 CHST3 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 4

 Carbohydrate sulfotransferase 4 ELISA Kit
 Carbohydrate sulfotransferase 4 Recombinant
 Carbohydrate sulfotransferase 4 Antibody
Also known as Carbohydrate sulfotransferase 4 (Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 3) (GST-3) (High endothelial cells N-acetylglucosamine 6-O-sulfotransferase) (HEC-GlcNAc6ST) (L-selectin ligand sulfotransferase) (LSST) (.
CHST4: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to posit
>>>
ion 6 of non-reducing N-acetylglucosamine (GlcNAc) residues within mucin-associated glycans that ultimately serve as SELL ligands. SELL ligands are present in high endothelial cells (HEVs) and play a central role in lymphocyte homing at sites of inflammation. Participates in biosynthesis of the SELL ligand sialyl 6-sulfo Lewis X on receptors SPN/CD43, GLYCAM1 and MADCAM1. Also involved in biosynthesis of SELL ligand recognized by MECA-79 antibody. Plays a central role in lymphocyte trafficking during chronic inflammation. Has a catalytic preference for core 2- branched mucin-type O-glycans. Can use GlcNAcbeta1-6[Galbeta1- 3]GalNAc-pNP (core 2), GlcNAcbeta1-6ManOMe and GlcNAcbeta1-2Man oligosaccharide structures as acceptors. Has also activity toward core 3 of GlcNAcbeta1-3GalNAc-pNP. Its substrate specificity may be influenced by its subcellular location. Belongs to the sulfotransferase 1 family. Gal/GlcNAc/GalNAc subfamily.

Protein type: EC 2.8.2.-; Glycan Metabolism - keratan sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 16q22.2

Cellular Component: Golgi membrane; integral to membrane; trans-Golgi network

Molecular Function: N-acetylglucosamine 6-O-sulfotransferase activity; sulfotransferase activity

Biological Process: cell adhesion; cell motility; cell-cell signaling; immune response; N-acetylglucosamine metabolic process; O-glycan processing; protein amino acid sulfation; sulfur metabolic process
 CHST4 ELISA Kit
 CHST4 Recombinant
 CHST4 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 5

 Carbohydrate sulfotransferase 5 ELISA Kit
 Carbohydrate sulfotransferase 5 Recombinant
 Carbohydrate sulfotransferase 5 Antibody
Also known as Carbohydrate sulfotransferase 5 (Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 4) (GST4) (Intestinal N-acetylglucosamine-6-O-sulfotransferase) (I-GlcNAc6ST) (Intestinal GlcNAc-6-sulfotransferase) (mIGn6ST) (N-acetylgl.
CHST6: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to posit
>>>
ion 6 of non-reducing N-acetylglucosamine (GlcNAc) residues of keratan. Mediates sulfation of keratan in cornea. Keratan sulfate plays a central role in maintaining corneal transparency. Acts on the non-reducing terminal GlcNAc of short and long carbohydrate substrates that have poly-N- acetyllactosamine structures. Defects in CHST6 are the cause of macular corneal dystrophy (MCD). MCD is an autosomal recessive disease characterized by corneal opacities. Onset occurs in the first decade, usually between ages 5 and 9. The disorder is progressive. Minute, gray, punctate opacities develop. Corneal sensitivity is usually reduced. Painful attacks with photophobia, foreign body sensations, and recurrent erosions occur in most patients. There are different types of MCD: MCD type I, in which there is a virtual absence of sulfated keratan sulfate (KS) in the serum and cornea, as determined by KS-specific antibodies; and MCD type II, in which the normal sulfated KS-antibody response is present in cornea and serum. MCD type I patients usually have a homozygous missense mutation, while MCD type II patients show a large deletion and replacement in the upstream region of CHST6. The only missense mutation for type II is Cys-50, which is heterozygous with a replacement in the upstream region on the other allele of CHST6. Belongs to the sulfotransferase 1 family. Gal/GlcNAc/GalNAc subfamily.

Protein type: EC 2.8.2.-; Glycan Metabolism - keratan sulfate biosynthesis; Membrane protein, integral; Transferase

Cellular Component: integral to membrane

Molecular Function: N-acetylglucosamine 6-O-sulfotransferase activity

Biological Process: keratan sulfate biosynthetic process; N-acetylglucosamine metabolic process; sulfur metabolic process
 Chst5 ELISA Kit
 Chst5 Recombinant
 Chst5 Antibody
 Gst4 ELISA Kit
 Gst4 Recombinant
 Gst4 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 6

 Carbohydrate sulfotransferase 6 ELISA Kit
 Carbohydrate sulfotransferase 6 Recombinant
 Carbohydrate sulfotransferase 6 Antibody
Also known as Carbohydrate sulfotransferase 6 (Corneal N-acetylglucosamine-6-O-sulfotransferase) (C-GlcNAc6ST) (hCGn6ST) (Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 4-beta) (GST4-beta) (N-acetylglucosamine 6-O-sulfotransferase 5.
CHST6: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to posit
>>>
ion 6 of non-reducing N-acetylglucosamine (GlcNAc) residues of keratan. Mediates sulfation of keratan in cornea. Keratan sulfate plays a central role in maintaining corneal transparency. Acts on the non-reducing terminal GlcNAc of short and long carbohydrate substrates that have poly-N- acetyllactosamine structures. Defects in CHST6 are the cause of macular corneal dystrophy (MCD). MCD is an autosomal recessive disease characterized by corneal opacities. Onset occurs in the first decade, usually between ages 5 and 9. The disorder is progressive. Minute, gray, punctate opacities develop. Corneal sensitivity is usually reduced. Painful attacks with photophobia, foreign body sensations, and recurrent erosions occur in most patients. There are different types of MCD: MCD type I, in which there is a virtual absence of sulfated keratan sulfate (KS) in the serum and cornea, as determined by KS-specific antibodies; and MCD type II, in which the normal sulfated KS-antibody response is present in cornea and serum. MCD type I patients usually have a homozygous missense mutation, while MCD type II patients show a large deletion and replacement in the upstream region of CHST6. The only missense mutation for type II is Cys-50, which is heterozygous with a replacement in the upstream region on the other allele of CHST6. Belongs to the sulfotransferase 1 family. Gal/GlcNAc/GalNAc subfamily.

Protein type: EC 2.8.2.-; Glycan Metabolism - keratan sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 16q22

Cellular Component: Golgi apparatus; Golgi membrane; integral to membrane

Molecular Function: N-acetylglucosamine 6-O-sulfotransferase activity

Biological Process: keratan sulfate biosynthetic process; N-acetylglucosamine metabolic process; sulfur metabolic process

Disease: Macular Dystrophy, Corneal, 1
 CHST6 ELISA Kit
 CHST6 Recombinant
 CHST6 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 7

 Carbohydrate sulfotransferase 7 ELISA Kit
 Carbohydrate sulfotransferase 7 Recombinant
 Carbohydrate sulfotransferase 7 Antibody
Also known as Carbohydrate sulfotransferase 7 (Chondroitin 6-sulfotransferase 2) (C6ST-2) (Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 5) (GST-5) (N-acetylglucosamine 6-O-sulfotransferase 4) (GlcNAc6ST-4) (Gn6st-4).
CHST7: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of non-re
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ducing N-acetylglucosamine (GlcNAc) residues. Preferentially acts on mannose-linked GlcNAc. Also able to catalyze the transfer of sulfate to position 6 of the N- acetylgalactosamine (GalNAc) residue of chondroitin. Also acts on core 2 mucin-type oligosaccharide and N-acetyllactosamine oligomer with a lower efficiency. Has weak or no activity toward keratan sulfate and oligosaccharides containing the Galbeta1-4GlcNAc. Catalyzes 6-O-sulfation of beta-benzyl GlcNAc but not alpha- or beta-benzyl GalNAc. Belongs to the sulfotransferase 1 family. Gal/GlcNAc/GalNAc subfamily.

Protein type: EC 2.8.2.17; Glycan Metabolism - chondroitin sulfate biosynthesis; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: Xp11.23

Cellular Component: Golgi membrane; integral to membrane

Molecular Function: chondroitin 6-sulfotransferase activity; N-acetylglucosamine 6-O-sulfotransferase activity

Biological Process: chondroitin sulfate biosynthetic process; N-acetylglucosamine metabolic process; polysaccharide metabolic process; sulfur metabolic process
 CHST7 ELISA Kit
 CHST7 Recombinant
 CHST7 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 8

 Carbohydrate sulfotransferase 8 ELISA Kit
 Carbohydrate sulfotransferase 8 Recombinant
 Carbohydrate sulfotransferase 8 Antibody
Also known as Carbohydrate sulfotransferase 8 (GalNAc-4-O-sulfotransferase 1) (GalNAc-4-ST1) (GalNAc4ST-1) (N-acetylgalactosamine-4-O-sulfotransferase 1).
CHST8: Catalyzes the transfer of sulfate to position 4 of non- reducing N-acetylgalactosamine (GalNAc) residues in both N-glycans and O-glycans. Required for biosynthesis of glycoprotein hormones lutropin and thyrotropin, by mediating sulfati
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on of their carbohydrate structures. Only active against terminal GalNAcbeta1,GalNAcbeta. Not active toward chondroitin. CHST8 mutations may be a cause of generalized non- inflammatory peeling skin syndrome type A (PubMed:22289416). Peeling skin syndrome (PSS) is a genodermatosis characterized by continuous shedding of the outer layers of the epidermis. Two main PSS subtypes have been suggested. Patients with non-inflammatory PSS (type A) manifest white scaling, with painless and easy removal of the skin, irritation when in contact with water, dust and sand, and no history of erythema, pruritis or atopy. Inflammatory PSS (type B) is associated with generalized erythema, pruritus and atopy. It is an ichthyosiform erythroderma characterized by lifelong patchy peeling of the entire skin with onset at birth or shortly after. Several patients have been reported with high IgE levels. Belongs to the sulfotransferase 2 family.

Protein type: EC 2.8.2.-; Membrane protein, integral; Transferase

Molecular Function: N-acetylgalactosamine 4-O-sulfotransferase activity

Biological Process: peptide hormone processing; proteoglycan biosynthetic process; sulfur metabolic process
 Chst8 ELISA Kit
 Chst8 Recombinant
 Chst8 Antibody
Table BarTOPTable Bar
 

Carbohydrate sulfotransferase 9

 Carbohydrate sulfotransferase 9 ELISA Kit
 Carbohydrate sulfotransferase 9 Recombinant
 Carbohydrate sulfotransferase 9 Antibody
Also known as Carbohydrate sulfotransferase 9 (GalNAc-4-O-sulfotransferase 2) (GalNAc-4-ST2) (GalNAc4ST-2) (N-acetylgalactosamine-4-O-sulfotransferase 2).
CHST9: Catalyzes the transfer of sulfate to position 4 of non- reducing N-acetylgalactosamine (GalNAc) residues in both N-glycans and O-glycans. Participates in biosynthesis of glycoprotein hormones lutropin and thyrotropin, by mediating sulf
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ation of their carbohydrate structures. Has a higher activity toward carbonic anhydrase VI than toward lutropin. Only active against terminal GalNAcbeta1,GalNAcbeta. Isoform 2, but not isoform 1, is active toward chondroitin. Belongs to the sulfotransferase 2 family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 2.8.2.-; Membrane protein, integral; Transferase

Chromosomal Location of Human Ortholog: 18q11.2

Cellular Component: Golgi membrane

Molecular Function: chondroitin 4-sulfotransferase activity; N-acetylgalactosamine 4-O-sulfotransferase activity

Biological Process: chondroitin sulfate biosynthetic process; hormone biosynthetic process; proteoglycan biosynthetic process; sulfur metabolic process
 CHST9 ELISA Kit
 CHST9 Recombinant
 CHST9 Antibody
 UNQ2549/PRO6175 ELISA Kit
 UNQ2549/PRO6175 Recombinant
 UNQ2549/PRO6175 Antibody
Table BarTOPTable Bar
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