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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)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Adenosine 5'-monophosphate sodium salt hydrate 99%
Supplier:
AMBEED, INC
Description:
1,2-Dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt ≥98%
Catalog Number:
(10391-010)
Supplier:
Bioss
Description:
Aldolase C (fructose bisphosphate aldolase) is a3å€ glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3 phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants which encode the same protein.
Catalog Number:
(102980-440)
Supplier:
Adipogen
Description:
Kynurenine aminotransferases (KATs) are pyridoxal-5’-phosphate-dependent enzymes that catalyze the conversion of L-kynurenine into kynurenic acid, a neuroactive metabolite whose unbalancing is associated with a number of brain disorders
Catalog Number:
(10110-552)
Supplier:
Prosci
Description:
NAGS is a mitochondrial enzyme that catalyzes the formation of N-acetylglutamate (NAG) from glutamate and acetyl coenzyme-A. NAG is a cofactor of carbamyl phosphate synthetase I (CPSI), the first enzyme of the urea cycle in mammals. Deficiencies in N-acetylglutamate synthase have been associated with hyperammonemia.The N-acetylglutamate synthase gene encodes a mitochondrial enzyme that catalyzes the formation of N-acetylglutamate (NAG) from glutamate and acetyl coenzyme-A. NAG is a cofactor of carbamyl phosphate synthetase I (CPSI), the first enzyme of the urea cycle in mammals. This gene may regulate ureagenesis by altering NAG availability and, thereby, CPSI activity. Deficiencies in N-acetylglutamate synthase have been associated with hyperammonemia.
Catalog Number:
(102116-296)
Supplier:
Novus Biologicals
Description:
Rabbit Polyclonal Mannose 6 Phosphate Receptor (Cation independent) Antibody. Tested Applications: Western Blot, Dot Blot, Immunocytochemistry/Immunofluorescence. Tested Reactivity: Human, Mouse, Bovine, Primate.
Supplier:
Electron Microscopy Sciences
Description:
Fixative Reagent Grade (Karnovsky’s). This fixative contains 3% glutaraldehyde and 2% formaldehyde in 0.1M phosphate buffer, pH 7.4. Karnovsky’s with formalin 2% and Biological glutaraldehyde 3% in 0.1m Phosphate Buffer. Karnovsky’s with paraformaldehyde solution and EM grade glutaraldehyde.
Supplier:
TCI America
Description:
CAS Number: 407-41-0
MDL Number: MFCD00065935
Molecular Formula: C3H8NO6P
Molecular Weight: 185.07
Purity/Analysis Method: <gt/>98.0% (T)
Form: Crystal
Melting point (°C): 167
Specific rotation [a]20/D: 5 deg (C=2, H2O)
Catalog Number:
(10100-566)
Supplier:
Prosci
Description:
Pyridoxal 5-prime-phosphate (PLP) is the active form of vitamin B6 that acts as a coenzyme in maintaining biochemical homeostasis. The preferred degradation route from PLP to 4-pyridoxic acid involves the dephosphorylation of PLP by PDXP.Pyridoxal 5-prime-phosphate (PLP) is the active form of vitamin B6 that acts as a coenzyme in maintaining biochemical homeostasis. The preferred degradation route from PLP to 4-pyridoxic acid involves the dephosphorylation of PLP by PDXP (Jang et al., 2003 [PubMed 14522954]).
Supplier:
MilliporeSigma
Description:
NADP, Disodium Salt, a coenzyme that is widely distributed in living matter. Participates in oxidation-reduction reactions.
Supplier:
HiMedia
Description:
For toxin detection in food products when clostridium botulinum is suspected.
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:
(76423-598)
Supplier:
Teknova
Description:
Teknova buffers are specifically formulated to comply with current molecular biology protocols.
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is still displayed and you need assistance, please call us at 1-800-932-5000.
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