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4-Amino-3-bromo-8-methoxyquinoline
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4-Amino-3-bromo-8-methoxyquinoline
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
Alcian Blue 8GX, also known as Ingrain Blue 1, is a basic copper phthalocyanine dye whose copper content imparts a blue color. It is tetravalent, cationic, and water-soluble in nature. It forms salt linkages with the acid groups of acid mucopolysaccharides.
Artikel-Nr:
(ACRO445220250)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
445220250
Lokale Artikelnummer::
ACRO445220250
Beschreibung:
Phenylboronsäurepinakolester 97%
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-10751R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10751R-CY3
Lokale Artikelnummer::
BOSSBS-10751R-CY3
Beschreibung:
Acts as an endocytic receptor mediating clathrin dependent endocytosis. Macrophage-restricted adhesion molecule that mediates sialic-acid dependent binding to lymphocytes, including granulocytes, monocytes, natural killer cells, B-cells and CD8 T-cells. Preferentially binds to alpha-2,3-linked sialic acid (By similarity). Binds to SPN/CD43 on T-cells (By similarity). May play a role in hemopoiesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10751R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10751R-CY5
Lokale Artikelnummer::
BOSSBS-10751R-CY5
Beschreibung:
Acts as an endocytic receptor mediating clathrin dependent endocytosis. Macrophage-restricted adhesion molecule that mediates sialic-acid dependent binding to lymphocytes, including granulocytes, monocytes, natural killer cells, B-cells and CD8 T-cells. Preferentially binds to alpha-2,3-linked sialic acid (By similarity). Binds to SPN/CD43 on T-cells (By similarity). May play a role in hemopoiesis.
VE:
1 * 100 µl
Lieferant:
Avantor
Beschreibung:
DILUT-IT dissolution media concentrates are produced from raw materials in accordance with USP/EP/BP/JP guidelines under validated processes in Avantor Performance Materials' ISO certified manufacturing facilities
Artikel-Nr:
(BOSSBS-9519R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9519R-A647
Lokale Artikelnummer::
BOSSBS-9519R-A647
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
Artikel-Nr:
(BOSSBS-9519R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9519R-CY5
Lokale Artikelnummer::
BOSSBS-9519R-CY5
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:
Sigma-Aldrich
Beschreibung:
Methanolic HCl (hydrogen chloride in methanol) is particularly useful for preparing methyl esters of volatile (short chain) fatty acids. Fatty acids are esterified by heating them with an anhydrous alcohol in the presence of an acidic catalyst in a sealed vessel at a high temperature for a short time. In the reaction, a fatty acid molecule and an alcohol molecule are joined, with the release of a water molecule. The derivatives can be quickly and easily recovered, quantitatively, from the reaction medium.
Artikel-Nr:
(BOSSBS-10751R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10751R-CY7
Lokale Artikelnummer::
BOSSBS-10751R-CY7
Beschreibung:
Acts as an endocytic receptor mediating clathrin dependent endocytosis. Macrophage-restricted adhesion molecule that mediates sialic-acid dependent binding to lymphocytes, including granulocytes, monocytes, natural killer cells, B-cells and CD8 T-cells. Preferentially binds to alpha-2,3-linked sialic acid (By similarity). Binds to SPN/CD43 on T-cells (By similarity). May play a role in hemopoiesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9519R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9519R-A750
Lokale Artikelnummer::
BOSSBS-9519R-A750
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 catalyses 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 1000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localised 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 characterised by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9519R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9519R
Lokale Artikelnummer::
BOSSBS-9519R
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
Artikel-Nr:
(BOSSBS-9519R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9519R-A350
Lokale Artikelnummer::
BOSSBS-9519R-A350
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:
Cayman Chemical
Beschreibung:
Rivastigmine is an irreversible inhibitor of acetylcholinesterase (IC<sub>50</sub>=4,15 µm) and butyrylcholinesterase (IC<sub>50</sub>=37 nM).
Artikel-Nr:
(BOSSBS-9519R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9519R-CY5.5
Lokale Artikelnummer::
BOSSBS-9519R-CY5.5
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
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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