tert-Butyl+2,9-diazaspiro[5.5]undecane-9-carboxylate+hydrochlorid
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.
Catalog Number:
(10109-130)
Supplier:
Prosci
Description:
Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology.Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology.
Catalog Number:
(RL601-1504)
Supplier:
Rockland Immunochemical
Description:
This product has been assayed against 1.0 µg of Bovine IgG in a standard capture ELISA using pNPP p-nitrophenyl phosphate as a substrate for 30 minutes at room temperature.
Catalog Number:
(10298-494)
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:
(10298-512)
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:
(76082-560)
Supplier:
Bioss
Description:
Catalyzes the phosphorylation of sphingosine to form sphingosine 1-phosphate (SPP), a lipid mediator with both intra- and extracellular functions. Also acts on D-erythro-dihydrosphingosine, D-erythro-sphingosine and L-threo-dihydrosphingosine. Binds phosphoinositides.
Catalog Number:
(76422-242)
Supplier:
Biolegend
Description:
F4/80, Recombinant Monoclonal Antibody, Clone: QA17A29, Host: Mouse, Species Reactivity: Mouse, Isotype: IgG1, K, Immunogen: Murine macrophages, Other Names: EMR1, Ly71, Formulation: Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide, Size: 500 uG
Catalog Number:
(76082-996)
Supplier:
Bioss
Description:
Required for the transport of mannose 6-phosphate receptors (MPR) from endosomes to the trans-Golgi network.
Supplier:
Promocell
Description:
These Dulbecco's PBS solution are used in tissue culture, cell isolation procedures and molecular biology.
Catalog Number:
(10065-298)
Supplier:
Hardy Diagnostics
Description:
For the preparation of specimens for AFB culture and other applications.
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Supplier:
MP Biomedicals
Description:
Deoxyribonuclease from beef pancreas, DNase I, was first crystallized by Kunitz. It is an endonuclease which splits phosphodiester linkages, preferentially adjacent to a pyrimidine nucleotide yielding 5'-phosphate terminated polynucleotides with a free hydroxyl group on position 3'. The average chain of limit digest is a tetranucleotide. DNase I acts upon single chain DNA, and upon double-stranded DNA and chromatin.
Catalog Number:
(103225-302)
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
Catalog Number:
(10278-258)
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.
Catalog Number:
(75933-862)
Supplier:
Rockland Immunochemical
Description:
Anti-Maltose Phosphorylase recognizes the protein maltose phosphorylase which belongs to the glycosyltransferases family. Maltose phosphorylase catalyzes the reaction in which maltose and inorganic phosphate are converted to D-glucose and beta-D-glucose 1-phosphate.
Catalog Number:
(IC10097880)
Supplier:
MP Biomedicals
Description:
One unit hydrolyzes 1 µmole of p-nitrophenyl thymidine-5-phosphate per minute at pH 8.9 and 25 °C.
Catalog Number:
(76237-620)
Supplier:
Rockland Immunochemical
Description:
Human IGF2R AccuSignal ELISA Kit
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