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Naphthol+AS-BI-phosphat+Dinatriumsalz


29 663  results were found

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Artikel-Nr: (APOSPC3086D-1G)

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: PC3086D-1G
Lokale Artikelnummer:: APOSPC3086D-1G
Beschreibung:   3,3'-Bis(trifluormethyl)benzhydrol 97%
VE:  1 * 1 g
Lieferant:  Thermo Scientific
Beschreibung:   1,1-Bis(methylthio)-2-nitroethylen 99%

Lieferant:  US Biological
Hersteller-Artikelnummer:: C0106-05
Lokale Artikelnummer:: USBIC0106-05
Beschreibung:   Anti-CAD Rabbit polyclonal antibody unconjugated
VE:  1 * 50 µl
Artikel-Nr: (APOSPC3107K-100MG)

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: PC3107K-100MG
Lokale Artikelnummer:: APOSPC3107K-100MG
Beschreibung:   3,5-Bis(trifluoromethyl)-N-ethylaniline 97%
VE:  1 * 100 mg
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13366R-A750
Lokale Artikelnummer:: BOSSBS-13366R-A750
Beschreibung:   GK2 is a 553 amino acid protein that belongs to the FGGY kinase family and is involved in the pathway of glycerol degradation. Localized to the outer membrane of the mitochondrion and expressed at high levels in testis, GK2 functions to catalyze the ATP-dependent conversion of glycerol to glycerol 3-phosphate. Via its catalytic activity, GK2 plays an essential role in the regulation of glycerol uptake and metabolism. The gene encoding GK2 maps to chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
VE:  1 * 100 µl
Lieferant:  LGC Standards PROMOCHEM
Hersteller-Artikelnummer:: NIST-694
Lokale Artikelnummer:: PROONIST-694
Beschreibung:   This standard material is intended to use in validating analytical methods and in calibrating instruments used in the analysis of phosphate rock, fertilisers and similar materials.
VE:  1 * 90 g
Lieferant:  Alfa Aesar
Beschreibung:   Phosphate-buffered saline (PBS) with EDTA, 5X, Liquid

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9036R-A555
Lokale Artikelnummer:: BOSSBS-9036R-A555
Beschreibung:   A scaffold protein that connects plasma membrane proteins and regulatory components, regulating their surface expression in epithelial cells apical domains. May be involved in the coordination of a diverse range of regulatory processes for ion transport and second messenger cascades. In complex with SLC9A3R1, may cluster proteins that are functionally dependent in a mutual fashion and modulate the trafficking and the activity of the associated membrane proteins. May play a role in the cellular mechanisms associated with multidrug resistance through its interaction with ABCC2 and PDZK1IP1. May potentiate the CFTR chloride channel activity. May function to connect SCARB1 with the cellular machineries for intracellular cholesterol transport and/or metabolism. May be involved in the regulation of proximal tubular Na(+)-dependent inorganic phosphate cotransport therefore playing an important role in tubule function.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9036R-A647
Lokale Artikelnummer:: BOSSBS-9036R-A647
Beschreibung:   A scaffold protein that connects plasma membrane proteins and regulatory components, regulating their surface expression in epithelial cells apical domains. May be involved in the coordination of a diverse range of regulatory processes for ion transport and second messenger cascades. In complex with SLC9A3R1, may cluster proteins that are functionally dependent in a mutual fashion and modulate the trafficking and the activity of the associated membrane proteins. May play a role in the cellular mechanisms associated with multidrug resistance through its interaction with ABCC2 and PDZK1IP1. May potentiate the CFTR chloride channel activity. May function to connect SCARB1 with the cellular machineries for intracellular cholesterol transport and/or metabolism. May be involved in the regulation of proximal tubular Na(+)-dependent inorganic phosphate cotransport therefore playing an important role in tubule function.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-9036R-CY5.5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9036R-CY5.5
Lokale Artikelnummer:: BOSSBS-9036R-CY5.5
Beschreibung:   A scaffold protein that connects plasma membrane proteins and regulatory components, regulating their surface expression in epithelial cells apical domains. May be involved in the coordination of a diverse range of regulatory processes for ion transport and second messenger cascades. In complex with SLC9A3R1, may cluster proteins that are functionally dependent in a mutual fashion and modulate the trafficking and the activity of the associated membrane proteins. May play a role in the cellular mechanisms associated with multidrug resistance through its interaction with ABCC2 and PDZK1IP1. May potentiate the CFTR chloride channel activity. May function to connect SCARB1 with the cellular machineries for intracellular cholesterol transport and/or metabolism. May be involved in the regulation of proximal tubular Na(+)-dependent inorganic phosphate cotransport therefore playing an important role in tubule function.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-9519R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9519R-CY3
Lokale Artikelnummer:: BOSSBS-9519R-CY3
Beschreibung:   BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease:Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) . A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.
VE:  1 * 100 µl
Lieferant:  Biotium
Beschreibung:   PLAP is a tissue specific, trophoblast-derived, 70 kDa, glycosyl-phosphatidylinositol (GPI)-anchored, dimeric, Zn2 metallo glycoprotein that catalyzes the hydrolysis of phosphomonoesters into an inorganic phosphate and an alcohol. It is present in the placenta and serum of pregnant women and in high frequency in gynecological and testicular cancers and in lower frequency in other tumors. The three tissue-specific AP's in humans, PLAP, germ cell AP (GCAP) and intestinal AP, are 90-98% homologous. Non-tissue specific AP is found in kidney, liver and bone. This MAb binds equally well to all common allelic variants (S, F, FS and I) of PLAP as to AP from normal human testis. This MAb can be used both as coating as well as tracer antibody in the same ELISA to detect PLAP in serum of S, F, FS and I phenotypes.

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13370R-A750
Lokale Artikelnummer:: BOSSBS-13370R-A750
Beschreibung:   The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8339R-A680
Lokale Artikelnummer:: BOSSBS-8339R-A680
Beschreibung:   The pantothenate kinase (PANK) family of proteins catalyzes the first step in coenzyme A (CoA) biosynthesis. Coenzyme A is an important coenzyme involved in the synthesis and oxidation of fatty acids, as well as the oxidation of pyruvate in the citric acid (Krebs) cycle. Pantothenate kinase 3 (PANK3) is a 370 amino acid member of the pantothenate kinase family that plays a role in the physiological regulation of the intracellular CoA concentration. Localised to the cytoplasm, PANK3 is regulated by feedback inhibition by CoA and its thioesters. PANK3 transfers a phosphate from ATP to pantothenate (Vitamin B5), resulting in formation of 4?-phosphopantothenate. Closely related to its family members, PANK1, PANK2 and PANK4, PANK3 is highly expressed in liver. Pantothenate kinase associated neurodegeneration (PKAN) results from mutations in the gene encoding PANK2, the only mitochondria targeted human PANK.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13370R-A680
Lokale Artikelnummer:: BOSSBS-13370R-A680
Beschreibung:   The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
VE:  1 * 100 µl
Lieferant:  Sigma-Aldrich
Hersteller-Artikelnummer:: PHR1456-2X1G
Lokale Artikelnummer:: SUPLPHR1456-2X1G
Beschreibung:   Organic Standard, Bis(2 ethylhexyl)maleate
VE:  1 * 2 ST
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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