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Dibenzyl+phosphate


9,225  results were found

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Supplier:  Bioss
Description:   GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.
Catalog Number: (EM8.20099.0250)

Supplier:  MilliporeSigma
Description:   Anilinium chloride for synthesis
MSDS SDS
Supplier:  HiMedia
Description:   For toxin detection in food products when <i>Clostridium botulinum</i> is suspected.
MSDS SDS
Supplier:  Thermo Scientific Chemicals
Description:   Liquid
MSDS SDS

Supplier:  Novus Biologicals
Description:   Mannose 6 Phosphate Receptor Polyclonal Antibody, Host: Goat, Conjugate: Biotin, Species: Human, Isotype: IgG, Immunogen: Mouse myeloma cell line NS0-derived recombinant human IGF-II R, Synonym: CD222 antigen, Application: WB, Flow, Block, Size: 50ug
Supplier:  Electron Microscopy Sciences
Description:   All of our Earle’s Balanced Salt Solution contains: Potassium Chloride, Sodium Chloride, Sodium Phosphate Monobasic, and D-glucose. Some formulations may contain additional components. All of the solutions are prepared 1X strength.
Minority or Woman-Owned Business Enterprise
Supplier:  BeanTown Chemical
Description:   CAS: 50-63-5; EC No: 200-055-2; MDL No: MFCD00069852; RTECS: VB2450000 Solid; Molecular Formula: C18H26ClN3·2H3PO4; MW: 515.87 Melting Point: 200° (decomposes)
MSDS SDS

Supplier:  Bioss
Description:   Esterifies acyl-group from acyl-ACP to the sn-1 position of glycerol-3-phosphate, an essential step in glycerolipid biosynthesis.
Supplier:  MilliporeSigma
Description:   Traceable to SRM from NIST and PTB.
MSDS SDS

Supplier:  Bioss
Description:   Esterifies acyl-group from acyl-ACP to the sn-1 position of glycerol-3-phosphate, an essential step in glycerolipid biosynthesis.

Supplier:  Bioss
Description:   GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.
Catalog Number: (10278-204)

Supplier:  Bioss
Description:   The PHEX a 749 amino acid protein that putatively consists of an intracellular, transmembrane and extracellular domain. PHEX mutations have been observed in 60-80% of hypophosphatemic rickets patients. The PHEX protein, which is a single-pass membrane protein, is also designated HYP, X-linked hypophosphatemia protein or metalloendopeptidase homolog PEX. PHEX plays an active role in bone and dentin mineralization and renal phosphate re-absorption. X-linked hypophosphatemic rickets, also designated HYP, is an X-linked dominant disorder characterized by impaired phosphate uptake in the kidney, which is likely to be caused by abnormal regulation of sodium phosphate cotransport in the proximal tubules. Clinical manifestations include skeletal deformities, growth failure, craniosynostosis, paravertebral calcifications, pseudofractures in lower extremities, and muscular hypotonia with onset in early childhood.

Supplier:  GLOBAL LIFE SCIENCES SOLUTIONS
Description:   Cytiva manufactures PBS utilizing USP raw materials formulated in USP Water for Injection quality water.
MSDS SDS
Supplier:  Electron Microscopy Sciences
Supplier:  MilliporeSigma
Description:   When diluted with water, concentrates can clean by themselves without leaving residues
MSDS SDS
Supplier:  Bioss
Description:   This gene encodes an enzyme, consisting of two identical proteins, which catalyzes the isomerization of glyceraldehydes 3-phosphate (G3P) and dihydroxy-acetone phosphate (DHAP) in glycolysis and gluconeogenesis. Mutations in this gene are associated with triosephosphate isomerase deficiency. Pseudogenes have been identified on chromosomes 1, 4, 6 and 7. Alternative splicing results in multiple transcript variants.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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