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Catalog Number: (CA101319-784)
Supplier: Teknova
Description: Carbon: 2% Raffinose, Nitrogen: 0.5% Ammonium Sulfate, Minus: Uracil.


Catalog Number: (TCT0840-025G)
Supplier: TCI America
Description: CAS Number: 80526-82-5
MDL Number: MFCD00036149
Molecular Formula: C4H13NO4S
Molecular Weight: 171.21
Purity/Analysis Method: >96.0% (T)
Form: Crystal
Color: White

Supplier: C&G Containers
Description: These plastic bottles are used for the collection of aqueous media for testing metals and a variety of inorganic parameters, including alkalinity, anions, acidity, cyanide, sulfate, and hardness.

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Supplier: C&G Containers
Description: These plastic bottles are used for testing metals and a variety of inorganic parameters including alkalinity, anions, acidity, cyanide, sulfate, and hardness.
Supplier: Bachem Americas
Description: This sulfated peptide isolated first from the skin of the Australian frog Litoria caerulea is a more potent secretagogue than its analog CCK-8. Ceruletide is applied in the diagnosis of pancreatic function and, in high dosage, for the induction of pancreatitis in experimental animals.

Catalog Number: (10391-496)
Supplier: Bioss
Description: Hydrolyzes cerebroside sulfate.


Catalog Number: (76109-918)
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: (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: (76109-920)
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: (CA97026-322)
Supplier: Hach
Description: BART biodetectors are excellent diagnostic tools to help identify the presence and activity of various bacteria. Sulfate Reducing Bacteria (SRB) are one of the most important agents in biofouling and can cause corrosion, clogging, fouling of the water, and increased hygiene risks.


Catalog Number: (RC68304)
Supplier: Ricca Chemical
Description: 10% (w/v) Aqueous (100 g/L). ASTM for Sulfate. Container: Glass.

Catalog Number: (CAPI23281)
Supplier: Thermo Scientific
Description: Formulation: 25mM ammonium ferrous sulfate Sufficient For: Use with aqueous- or lipid-compatible procedures 1mL

Catalog Number: (10407-834)
Supplier: Bioss
Description: This gene encodes the perlecan protein, which consists of a core protein to which three long chains of glycosaminoglycans(heparan sulfate or chondroitin sulfate) are attached. The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules. It has been shown that this protein interacts with laminin, prolargin, collagen type IV, FGFBP1, FBLN2, FGF7 and Transthyretin, etc. and plays essential roles in multiple biological activities. Perlecan is a key component of the vascular extracellular matrix, where it helps to maintain the endothelial barrier function. It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis. It can also promote growth factor (e.g., FGF2) activity and thus stimulate endothelial growth and re-generation. It is a major component of basement membranes, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion. Mutations in this gene cause Schwartz-Jampel syndrome type 1, Silverman-Handmaker type of dyssegmental dysplasia, and Tardive dyskinesia.[provided by RefSeq, Mar 2010].


Catalog Number: (CAPIPA5-18591)
Supplier: Thermo Scientific
Description: This antibody is predicted to react with human and rat based on sequence homology. The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy , a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.


Catalog Number: (CAPIPA526584)
Supplier: Thermo Scientific
Description: SGSH is one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.


Catalog Number: (CA95020-944)
Supplier: HiMedia
Description: For the microbiological assay of polymyxin B, colistin sulfate, and colistimethate sodium.

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