You Searched For: Tributyrin+(Glycerol+tributyrate)

Supplier: Avantor

Description: Glycerine (vegetable based) 99.0-101.0% (by anhydrous basis) USP, J.T.Baker®

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Catalog Number: (BOSSBS-13366R-CY3)

Supplier: Bioss

Description: 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

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Catalog Number: (ABEB6761-02/40)

Supplier: Abeba

Description: <p>Slip resistance on ceramic, coated with SLS solution and on steel, coated with glycerol - slip resistance on ceramic substrate, covered with SLS solution and on steel substrate, covered with glycerol.</p>

UOM: 1 * 1 items

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Catalog Number: (BOSSBS-1253R-A750)

Supplier: Bioss

Description: Water channel required to promote glycerol permeability and water transport across cell membranes. Acts as a glycerol transporter in skin and plays an important role in regulating SC (stratum corneum) and epidermal glycerol content. Involved in skin hydration, wound healing, and tumorigenesis. Provides kidney medullary collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient. Slightly permeable to urea and may function as a water and urea exit mechanism in antidiuresis in collecting duct cells. It may play an important role in gastrointestinal tract water transport and in glycerol metabolism.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-13366R)

Supplier: Bioss

Description: 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

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Catalog Number: (BOSSBS-13366R-A350)

Supplier: Bioss

Description: 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

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Supplier: Apollo Scientific

Description: 3-(2-Ethylhexyloxy)-1,2-propanediol

Supplier: Thermo Fisher Scientific

Description: CAS No.: 555-45-3

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Catalog Number: (BOSSBS-1253R-A680)

Supplier: Bioss

Description: Water channel required to promote glycerol permeability and water transport across cell membranes. Acts as a glycerol transporter in skin and plays an important role in regulating SC (stratum corneum) and epidermal glycerol content. Involved in skin hydration, wound healing, and tumorigenesis. Provides kidney medullary collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient. Slightly permeable to urea and may function as a water and urea exit mechanism in antidiuresis in collecting duct cells. It may play an important role in gastrointestinal tract water transport and in glycerol metabolism.

UOM: 1 * 100 µl

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Catalog Number: (USBIG8153-25-BIOT)

Supplier: US Biological

Description: Anti-GK2 Rabbit Polyclonal Antibody (Biotin)

UOM: 1 * 200 µl

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Supplier: Thermo Fisher Scientific

Description: Monoacetin mixture of isomers cont. varying amounts of diacetate, tech.

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Supplier: Thermo Fisher Scientific

Description: (R)-(-)-Epichlorhydrin ≥98%

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Catalog Number: (LIOF412430)

Supplier: LIOFILCHEM

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

UOM: 1 * 1 items

Certificates Sale

Catalog Number: (BOSSBS-13366R-FITC)

Supplier: Bioss

Description: 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

Sale

Catalog Number: (BOSSBS-13366R-A488)

Supplier: Bioss

Description: 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

Sale

Supplier: Thermo Fisher Scientific

Description: Appearance: Clear colorless Liquid

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