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Catalog Number: (10391-474)
Supplier: Bioss
Description: Hydrolyzes cerebroside sulfate.


Catalog Number: (CXK-5530)
Supplier: CHEMetrics
Description: The Titrets® test uses a ceric sulfate titrant with ferroin indicator. Depending on the procedure used, this kit can determine H2O2 concentrations from 0.01% to as high as 20%.

SDS Small Business Enterprise


Supplier: CHEMetrics
Description: Ceric sulfate is the titrant and ferroin is the end point indicator. The method is free from glycol interference in samples that contain up to 75% glycol, making it particularly applicable to systems that contain nitrite corrosion inhibitors. Results are expressed as ppm (mg/L) NaNO2.

SDS Small Business Enterprise

Catalog Number: (89268-628)
Supplier: Genetex
Description: Rabbit polyclonal antibody to HS6ST3 (C-terminal)


Catalog Number: (76203-084)
Supplier: MP Biomedicals
Description: YNB is a well defined composition of salts and vitamins for a vigorous growth of <i>S. cerevisiae.</i>


Supplier: Thermo Scientific Chemicals
Description: Antibiotic. Inhibits translocation during protein biosynthesis
Catalog Number: (10097-198)
Supplier: Proteintech
Description: XYLT1, also named as XT1, Belongs to the glycosyltransferase 14 family and XylT subfamily. It catalyzes the first step in biosynthesis of glycosaminoglycan. XYLT1 transfers D-xylose from UDP-D-xylose to specific serine residues of the core protein. Initial enzyme in the biosynthesis of chondroitin sulfate and dermatan sulfate proteoglycans in fibroblasts and chondrocytes. The antibody is specific to XYLT1.


Catalog Number: (10667-114)
Supplier: Bioss
Description: Sulfatases hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling and degradation of macromolecules. Arylsulfatase H, also known as ARSH, is a 562 amino acid protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Localized to the plasma membrane, Arylsulfatase H uses calcium as a cofactor to hydrolyze sulfate esters. The gene encoding Arylsulfatase D maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.


Catalog Number: (10391-318)
Supplier: Bioss
Description: Involved in translocation of malonate, malate and succinate in exchange for phosphate, sulfate, sulfite or thiosulfate across mitochondrial inner membrane.


Catalog Number: (89365-190)
Supplier: Genetex
Description: CCKB receptor, also called gastrin receptor, is a Cholecystokinin Receptor. CCKB receptor binds both sulfated and non-sulfated cholecystokinin analogs. This receptor regulates anxiety, arousal, opiate-induced analgesia, and gastric-acid secretion. CCKB receptor has been reported in brain, colon, pancreas, stomach, thyroid, and various cancers. ESTs have been isolated from normal eye libraries and libraries derived from cancers of the brain, embryo, germ cell, lung, and placenta.


Catalog Number: (10391-328)
Supplier: Bioss
Description: Involved in translocation of malonate, malate and succinate in exchange for phosphate, sulfate, sulfite or thiosulfate across mitochondrial inner membrane.


Catalog Number: (10667-120)
Supplier: Bioss
Description: Sulfatases hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling and degradation of macromolecules. Arylsulfatase H, also known as ARSH, is a 562 amino acid protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Localized to the plasma membrane, Arylsulfatase H uses calcium as a cofactor to hydrolyze sulfate esters. The gene encoding Arylsulfatase D maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.


Catalog Number: (CA1.08294.0005)
Supplier: MilliporeSigma
Description: Cas Number 3688-92-4, Indicator For Sulfate Titration

Catalog Number: (CAPIPA5-18808)
Supplier: Thermo Scientific
Description: This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate. Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme. Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder.


Catalog Number: (10103-734)
Supplier: Prosci
Description: B3GALT6 (Beta-1,3-galactosyltransferase) transfers galactose from UDP-galactose to substrates with a terminal beta-linked galactose residue. It has a preference for galactose-beta-1,4-xylose that is found in the linker region of glycosaminoglycans, such as heparan sulfate and chondroitin sulfate. It has no activity towards substrates with terminal glucosamine or galactosamine residues.


Catalog Number: (76102-062)
Supplier: Bioss
Description: Cell surface proteoglycan that bears heparan sulfate. Binds, via the heparan sulfate side chains, alpha-4 (V) collagen and participates in Schwann cell myelination (By similarity). May act as a catalyst in increasing the rate of conversion of prion protein PRPN(C) to PRNP(Sc) via associating (via the heparan sulfate side chains) with both forms of PRPN, targeting them to lipid rafts and facilitating their interaction. Required for proper skeletal muscle differentiation by sequestering FGF2 in lipid rafts preventing its binding to receptors (FGFRs) and inhibiting the FGF-mediated signaling.


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