Esta buscando: 8-Bromoquinoline-4-carbonitrile


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Descripción: Liofilchem® is present in over 60 countries with agents and distributors placing the products around the world.
Numero del catalogo: LIOF412430
UOM: 1 * 1 UN
Proveedor: LIOFILCHEM

Certificados


Descripción: 50 mM HEPES, pH 7,4, 100 mM NaCl, 0,1% CHAPS, 10 mM DTT, 1 mM EDTA, 10% glycerol.
Numero del catalogo: ENZOBMLKI1110020
UOM: 1 * 20 mL
Proveedor: ENZO LIFE SCIENCES


Descripción: Monoacetin (Mezcla de isómeros) cont. varying amounts of diacetate, tech.
Numero del catalogo: A14025.30
UOM: 1 * 250 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Descripción: 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.
Numero del catalogo: BOSSBS-13366R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: The protein encoded by this gene localises to the inner mitochondrial membrane and catalyses the conversion of glycerol-3-phosphate to dihydroxyacetone phosphate, using FAD as a cofactor. Along with GDP1, the encoded protein constitutes the glycerol phosphate shuttle, which reoxidises NADH formed during glycolysis. Two transcript variants encoding the same protein have been found for this gene.
Numero del catalogo: BOSSBS-4061R-A680
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: (±)-Epiclorohidrina ≥99%
Numero del catalogo: A15823.36
UOM: 1 * 500 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Descripción: (±)-Epiclorohidrina ≥99.0% (por GC)
Numero del catalogo: TCIAE0012-25G
UOM: 1 * 25 g
Proveedor: TCI


Descripción: Sample buffer for protein electrophoresis.
Numero del catalogo: ROCKMB-018
UOM: 1 * 100 mL
Proveedor: Rockland Immunochemicals


Descripción: (S)-(+)-Epiclorohidrina
Numero del catalogo: APOSOR28971-25G
UOM: 1 * 25 g
Proveedor: Apollo Scientific


Descripción: 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.
Numero del catalogo: BOSSBS-13366R-A647
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: (S)-(+)-Epiclorohidrina ≥98.0% (por GC)
Numero del catalogo: TCIAE0533-5G
UOM: 1 * 5 g
Proveedor: TCI


Descripción: 3-(2-Ethylhexyloxy)-1,2-propanediol ≥98.0% (por GC)
Numero del catalogo: TCIAE1044-25ML
UOM: 1 * 25 mL
Proveedor: TCI

Certificados


Descripción: Glicerina ≥99.0% (por GC) para electroforesis
Numero del catalogo: TCIAG0316-1G
UOM: 1 * 1 g
Proveedor: TCI


Descripción: 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.
Numero del catalogo: BOSSBS-13366R-CY7
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: 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.
Numero del catalogo: BOSSBS-13366R-HRP
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: 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.
Numero del catalogo: BOSSBS-13366R-A555
UOM: 1 * 100 µl
Proveedor: Bioss


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