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n-Butyl+phosphate
Artikel-Nr:
(BOSSBS-4159R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4159R-A680
Lokale Artikelnummer::
BOSSBS-4159R-A680
Beschreibung:
Catalytic subunit of the PI3K complex that mediates formation of phosphatidylinositol 3-phosphate which plays a key role in initiation and maturation of autophagosomes. Involved in the transport of lysosomal enzyme precursors to lysosomes. Required for the abcission step in cytokinesis. Required for transport from early to late endosomes.
VE:
1 * 100 µl
Artikel-Nr:
(PRSI27-199)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
27-199
Lokale Artikelnummer::
PRSI27-199
Beschreibung:
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]).
VE:
1 * 50 µG
Artikel-Nr:
(PRSI91-948)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
91-948
Lokale Artikelnummer::
PRSI91-948
Beschreibung:
Fructose-1,6-bisphosphatase 1(FBP1) is a homotetramer protein and belongs to the FBPase class 1 family. It involves in carbohydrate biosynthesis; gluconeogenesis pathway. FBP1 is a gluconeogenesis regulatory protein which catalyses the hydrolysis of fructose 1,6-bisphosphate to fructose 6-phosphate and inorganic phosphate. FBP1 deficiency is associated with hypoglycemia and metabolic acidosis. FBP1 regulates mouse endogenous glucose production. FBP1 coupled with phosphofructokinase (PFK) takes part in the metabolism of pancreatic islet cells.
VE:
1 * 50 µG
Artikel-Nr:
(APOSOR1008491-250)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR1008491-250
Lokale Artikelnummer::
APOSOR1008491-250
Beschreibung:
(R)-3,3-Bis(1-Naphthalenyl)-1,1-Binaphthyl-2,2-Diyl Hydrogen Phosphate 250mg pack 1 * 250 mg
VE:
1 * 250 mg
New Product
Artikel-Nr:
(APOSOR1008698-100)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR1008698-100
Lokale Artikelnummer::
APOSOR1008698-100
Beschreibung:
(S)-3,3-Bis(2-Naphthalenyl)-1,1-Binaphthyl-2,2-Diyl Hydrogen Phosphate 100mg pack 1 * 100 mg
VE:
1 * 100 mg
New Product
Artikel-Nr:
(APOSOR52282-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR52282-250MG
Lokale Artikelnummer::
APOSOR52282-250MG
Beschreibung:
(R)-3,3'-Bis(9-phenanthryl)-1,1'-binaphthalene-2,2'-diyl hydrogen phosphate 250mg pack 1 * 250 mg
VE:
1 * 250 mg
New Product
Artikel-Nr:
(PRSI3781)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
3781
Lokale Artikelnummer::
PRSI3781
Beschreibung:
GAPDH Antibody: Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) catalyzes the reversible oxidative phosphorylation of glyceraldehyde-3-phosphate in the presence of inorganic phosphate and nicotinamide adenine dinucleotide (NAD), an important energy-yielding step in carbohydrate metabolism. Recent evidence suggests that it also is involved in a number of cellular processes such as membrane fusion, phosphotransferase activity, DNA replication and repair, and nuclear RNA export. GAPDH has also been implicated in playing a role in different pathologies such as cancer progression, apoptosis, and neuronal diseases such as Alzheimer's and Huntington's disease. GAPDH is constitutively expressed at high levels in almost all tissues and cell lines making it ideal for use as a loading control marker in immunoblots.
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-5581R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5581R-A750
Lokale Artikelnummer::
BOSSBS-5581R-A750
Beschreibung:
Catalytic subunit of the PI3K complex that mediates formation of phosphatidylinositol 3-phosphate which plays a key role in initiation and maturation of autophagosomes. Involved in the transport of lysosomal enzyme precursors to lysosomes. Required for the abcission step in cytokinesis. Required for transport from early to late endosomes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13461R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13461R
Lokale Artikelnummer::
BOSSBS-13461R
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13461R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13461R-HRP
Lokale Artikelnummer::
BOSSBS-13461R-HRP
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10419R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10419R-HRP
Lokale Artikelnummer::
BOSSBS-10419R-HRP
Beschreibung:
This gene belongs to the GPI family whose members encode multifunctional phosphoglucose isomerase proteins involved in energy pathways. The protein encoded by this gene is a dimeric enzyme that catalyzes the reversible isomerization of glucose-6-phosphate and fructose-6-phosphate. The protein functions in different capacities inside and outside the cell. In the cytoplasm, the gene product is involved in glycolysis and gluconeogenesis, while outside the cell it functions as a neurotrophic factor for spinal and sensory neurons. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3976R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3976R
Lokale Artikelnummer::
BOSSBS-3976R
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13461R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13461R-FITC
Lokale Artikelnummer::
BOSSBS-13461R-FITC
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR52282-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR52282-100MG
Lokale Artikelnummer::
APOSOR52282-100MG
Beschreibung:
(R)-3,3'-Bis(9-phenanthryl)-1,1'-binaphthalene-2,2'-diyl hydrogen phosphate 100mg pack 1 * 100 mg
VE:
1 * 100 mg
New Product
Artikel-Nr:
(BOSSBS-10419R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10419R
Lokale Artikelnummer::
BOSSBS-10419R
Beschreibung:
This gene belongs to the GPI family whose members encode multifunctional phosphoglucose isomerase proteins involved in energy pathways. The protein encoded by this gene is a dimeric enzyme that catalyzes the reversible isomerization of glucose-6-phosphate and fructose-6-phosphate. The protein functions in different capacities inside and outside the cell. In the cytoplasm, the gene product is involved in glycolysis and gluconeogenesis, while outside the cell it functions as a neurotrophic factor for spinal and sensory neurons. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13461R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13461R-A555
Lokale Artikelnummer::
BOSSBS-13461R-A555
Beschreibung:
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.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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