Esta buscando: 2-Oleoyl+Glycerol

Numero del catalogo: (LIOF412430)

Proveedor: LIOFILCHEM

Descripción: Liofilchem® is present in over 60 countries with agents and distributors placing the products around the world.

UOM: 1 * 1 UN

Certificados Promoción

Numero del catalogo: (ENZOBMLKI1110020)

Proveedor: ENZO LIFE SCIENCES

Descripción: 50 mM HEPES, pH 7,4, 100 mM NaCl, 0,1% CHAPS, 10 mM DTT, 1 mM EDTA, 10% glycerol.

UOM: 1 * 20 mL

Promoción

Proveedor: Thermo Fisher Scientific

Descripción: Monoacetin (Mezcla de isómeros) cont. varying amounts of diacetate, tech.

FDS Certificados

Numero del catalogo: (BOSSBS-13366R-CY5)

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.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-4061R-A680)

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.

UOM: 1 * 100 µl

Promoción

Proveedor: Thermo Fisher Scientific

Descripción: (±)-Epiclorohidrina ≥99%

FDS Certificados

Proveedor: TCI

Descripción: (±)-Epiclorohidrina ≥99.0% (por GC)

Numero del catalogo: (ROCKMB-018)

Proveedor: Rockland Immunochemicals

Descripción: Sample buffer for protein electrophoresis.

UOM: 1 * 100 mL

Promoción

Proveedor: Apollo Scientific

Descripción: (S)-(+)-Epiclorohidrina

Numero del catalogo: (BOSSBS-13366R-A647)

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.

UOM: 1 * 100 µl

Promoción

Proveedor: TCI

Descripción: (S)-(+)-Epiclorohidrina ≥98.0% (por GC)

Numero del catalogo: (TCIAE1044-25ML)

Proveedor: TCI

Descripción: 3-(2-Ethylhexyloxy)-1,2-propanediol ≥98.0% (por GC)

UOM: 1 * 25 mL

Certificados Promoción

Numero del catalogo: (TCIAG0316-1G)

Proveedor: TCI

Descripción: Glicerina ≥99.0% (por GC) para electroforesis

UOM: 1 * 1 g

Promoción

Numero del catalogo: (BOSSBS-13366R-CY7)

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.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-13366R-HRP)

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.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-13366R-A555)

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.

UOM: 1 * 100 µl

Promoción