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Descripción: These seagrass preparations are available sets of five.
Numero del catalogo: 763-0384
UOM: 1 * 1 SET
Proveedor: LIEDER JOHANNES


Descripción: Las variantes de bombas peristálticas VWR® ofrecen una selección de bombas de alimentación con diferentes cabezales de bomba integrados en la carcasa de la bomba. Cubren un amplio espectro de áreas de aplicación en el laboratorio y en la industria.
Numero del catalogo: 181-0593
UOM: 1 * 1 UN
Proveedor: VWR Collection


Descripción: Bomba peristáltica para la preparación de medios de cultivo. Úselo para la dispensación en serie de medios de cultivo, agar o cualquier diluyente líquido para una preparación eficiente de la muestra.
Numero del catalogo: 710-2126
UOM: 1 * 1 UN
Proveedor: VWR Collection


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-A555
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-A680
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-CY3
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-A488
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Filtro de neblina de aceite completo, 10/16 para bombas RVP, con cartucho de filtro: montaje directo en la brida de escape de la bomba
Numero del catalogo: 181-7002
UOM: 1 * 1 UN
Proveedor: VWR Collection


Descripción: VWR® peristaltic pump variants offer a selection of dosing pumps with different pump heads integrated into the pump housing. They cover a broad spectrum of application areas in the laboratory and in industry.
Numero del catalogo: 181-0596
UOM: 1 * 1 UN
Proveedor: VWR Collection


Descripción: Aceite de bomba de vacío, VWR RV+ aceite, 1 L
Numero del catalogo: 181-0514
UOM: 1 * 5 L
Proveedor: VWR Collection

FDS


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-FITC
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-CY7
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Bomba peristáltica, VWR®, Trocar para bolsas de caldo
Numero del catalogo: 710-2127
UOM: 1 * 1 UN
Proveedor: VWR Collection


Descripción: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterised by mental retardation and the widespread development of distinctive tumors termed hamartomas. Two different genetic loci have been linked to TSC; one of these loci, the tuberous sclerosis-2 gene (TSC2), encodes a protein called tuberin and the other loci, tuberous sclerosis-1 gene (TSC1), encodes a protein called hamartin. Tuberin and hamartin interact with each other forming a cystoplasmic complex. Hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins and inhibition of hamartin activity results in loss of cell adhesion. Hamartin is present in most adult tissues with strong expression in brain, heart, and kidney.
Numero del catalogo: BOSSBS-15406R-A350
UOM: 1 * 100 µl
Proveedor: Bioss


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