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Carbohydrate (N-Acetylglucosamine 6-O) Sulfotransferase 6 (CHST6) ELISA Kits

The protein encoded by CHST6 is an enzyme that catalyzes the transfer of a sulfate group to the GlcNAc residues of keratan. Additionally we are shipping CHST6 Antibodies (43) and CHST6 Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
CHST6 4166 Q9GZX3
CHST6    
CHST6    
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Top CHST6 ELISA Kits at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Mouse
96 Tests Log in to see 16 to 21 Days
$999.43
Details
Rat
96 Tests Log in to see 16 to 21 Days
$999.43
Details
Human
96 Tests Log in to see 16 to 21 Days
$999.43
Details

More ELISA Kits for CHST6 Interaction Partners

Human Carbohydrate (N-Acetylglucosamine 6-O) Sulfotransferase 6 (CHST6) interaction partners

  1. Three novel and six previously reported disease-causing CHST6 mutations were identified in Korean patients with macular corneal dystrophy.

  2. Homozygous or compound heterozygous CHST6 mutations were identified in all cases, including two novel mutations, c.13C>T; p.(Arg5Cys) and c.289C>T; p.(Arg97Cys).

  3. This novel gene mutation expands the mutation spectrum of the CHST6 gene and contributes to the study of molecular pathogenesis of corneal dystrophy.

  4. This study improves the knowledge of the genetic features of Mexican patients with corneal stromal dystrophies by identifying mutations in the TGFBI (show TGFBI ELISA Kits), CHST6, and GSN (show GSN ELISA Kits) genes.

  5. Macular corneal dystrophy (MCD (show MLYCD ELISA Kits)) may result from other changes in the regulatory elements of CHST6 or from genetic heterogeneity.

  6. analysis of pathogenic mutations of TGFBI (show TGFBI ELISA Kits) and CHST6 genes in Chinese patients with Avellino, lattice, and macular corneal dystrophies

  7. CHST6 gene sequencing revealed 2 heterozygous mutations in case 1, a p.Arg211Gln and a novel mutation of p.Arg177Gly and a novel homozygous mutation of p.Pro186Arg in case 2.

  8. CHST6 mutations may be responsible for the pathogenesis of macular corneal dystrophy (MCD) in Chinese patients.

  9. Novel mutations are thought to result in loss of corneal sulfotransferase function.

  10. patients with MCD (show MLYCD ELISA Kits) (macular corneal dystrophy) combined with those reported in previous studies indicated CHST6 mutational heterogeneity.

CHST6 Antigen Profile

Antigen Summary

The protein encoded by this gene is an enzyme that catalyzes the transfer of a sulfate group to the GlcNAc residues of keratan. Keratan sulfate helps maintain corneal transparency. Defects in this gene are a cause of macular corneal dystrophy (MCD).

Gene names and symbols associated with CHST6

  • carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6 (chst6) antibody
  • carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6 (CHST6) antibody
  • MCDC1 antibody

Protein level used designations for CHST6

carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6 , carbohydrate sulfotransferase 6-like , carbohydrate sulfotransferase 5 , C-GlcNAc6ST , GST4-beta , N-acetylglucosamine 6-O-sulfotransferase 5 , carbohydrate sulfotransferase 6 , corneal N-acetylglucosamine 6-sulfotransferase , corneal N-acetylglucosamine-6-O-sulfotransferase , galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 4-beta , glcNAc6ST-5 , gn6st-5 , hCGn6ST

GENE ID SPECIES
444431 Xenopus laevis
711570 Macaca mulatta
736759 Pan troglodytes
100437082 Pongo abelii
100477677 Ailuropoda melanoleuca
770257 Gallus gallus
4166 Homo sapiens
538464 Bos taurus
489707 Canis lupus familiaris
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