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4-Ethyl-o-xylene
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4-Ethyl-o-xylene
Catalog Number:
(10298-508)
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:
(10100-048)
Supplier:
Prosci
Description:
GMPPA is a GDP-mannose pyrophosphorylase. This enzyme catalyzes the reaction which converts mannose-1-phosphate and GTP to GDP-mannose which is involved in the production of N-linked oligosaccharides.This gene is thought to encode a GDP-mannose pyrophosphorylase. This enzyme catalyzes the reaction which converts mannose-1-phosphate and GTP to GDP-mannose which is involved in the production of N-linked oligosaccharides.
Catalog Number:
(10392-038)
Supplier:
Bioss
Description:
Transaldolase 1 is a key enzyme of the nonoxidative pentose phosphate pathway providing ribose-5-phosphate for nucleic acid synthesis and NADPH for lipid biosynthesis. This pathway can also maintain glutathione at a reduced state and thus protect sulfhydryl groups and cellular integrity from oxygen radicals. The functional gene of transaldolase 1 is located on chromosome 11 and a pseudogene is identified on chromosome 1 but there are conflicting map locations. The second and third exon of this gene were developed by insertion of a retrotransposable element. This gene is thought to be involved in multiple sclerosis.
Catalog Number:
(10104-590)
Supplier:
Prosci
Description:
FN3KRP phosphorylates psicosamines and ribulosamines, but not fructosamines, on the third carbon of the sugar moiety. Protein-bound psicosamine 3-phosphates and ribulosamine 3-phosphates are unstable and decompose under physiological conditions. Thus phosphorylation leads to deglycation.FN3KRP and FN3K (MIM 608425) protect proteins from nonenzymatic glycation by phosphorylating the modified amino acid. This phosphorylation destabilizes the sugar-amine linkage and leads to spontaneous decomposition (Conner et al., 2004 [PubMed 15381090]).
Supplier:
Chem Impex International
Description:
HEPES is used as a hydrogen ion buffer, which can control the constant pH range for long term.
Supplier:
MilliporeSigma
Description:
For elemental metal analysis via atomic absorption and ICP instruments. Actual Lot Analysis on label. Color-coded label to match acid cap.
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:
(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:
(76081-692)
Supplier:
Lucigen
Description:
Specifically dephosphorylate 5´-triphosphorylated RNA, such as primary RNA transcripts, but not 5´-capped mRNA
Supplier:
Biosynth International Inc
Description:
Phytic acid, dodecasodium salt is used as cell biology, storage form of phosphorus in plant tissues, core bioreagents, functional foods
Catalog Number:
(100505-062)
Supplier:
Electron Microscopy Sciences
Description:
Used to adjust the pH of buffers and fixative solutions.
Catalog Number:
(76371-714)
Supplier:
Argos Technologies
Description:
Ideal for field calibration 'on the go'.
Catalog Number:
(10486-216)
Supplier:
Bioss
Description:
Repair polymerase that plays a key role in base-excision repair. Has 5'-deoxyribose-5-phosphate lyase (dRP lyase) activity that removes the 5' sugar phosphate and also acts as a DNA polymerase that adds one nucleotide to the 3' end of the arising single-nucleotide gap. Conducts 'gap-filling' DNA synthesis in a stepwise distributive fashion rather than in a processive fashion as for other DNA polymerases.
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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
is still displayed and you need assistance, please call us at 1-800-932-5000.
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