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Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
Numero del catalogo: BOSSBS-13370R-A750
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
Numero del catalogo: BOSSBS-13370R-HRP
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
Numero del catalogo: BOSSBS-13370R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
Numero del catalogo: BOSSBS-13370R-A350
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
Numero del catalogo: BOSSBS-13370R
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.
Numero del catalogo: BOSSBS-13370R-A488
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Tris-(hidroximetil) aminometano clorhidrato, Millipore®
Numero del catalogo: 648313-500
UOM: 1 * 500 g
Proveedor: Merck Millipore (Calbiochem‎)


Descripción: Solubility (5% aq soln) clear, colorless solution.
Numero del catalogo: ICNA04816124
UOM: 1 * 500 g
Proveedor: MP Biomedicals


Descripción: Alizarina complexona
Numero del catalogo: ICNA0520342901
UOM: 1 * 1 g
Proveedor: MP Biomedicals


Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol)
Numero del catalogo: EHERC17894900
UOM: 1 * 0,1 g
Proveedor: EHRENSTORFER


Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol)
Numero del catalogo: RC-105
UOM: 1 * 500 g
Proveedor: G-Biosciences


Descripción: Alizarina complexona ∼85% for the determination of fluorine, Fluka™
Numero del catalogo: 05590-5G
UOM: 1 * 5 g
Proveedor: Honeywell Chemicals


Descripción: Tris-(hidroximetil) aminometano clorhidrato
Numero del catalogo: RC-108
UOM: 1 * 1 kg
Proveedor: G-Biosciences


Descripción: Tris-(hidroximetil) aminometano clorhidrato, EMPROVE® EXPERT para producción biofarmacéutica, SAFC®
Numero del catalogo: 1.08219.9012
UOM: 1 * 12 kg
Proveedor: MERCK PRODUCTION CHEMICALS

FDS Certificados


Descripción: Tris-(hidroximetil) aminometano clorhidrato, Millipore®
Numero del catalogo: 648317-1
UOM: 1 * 1 kg
Proveedor: Merck Millipore (Calbiochem‎)


Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol), Millipore®
Numero del catalogo: 648311-1
UOM: 1 * 1 kg
Proveedor: Merck Millipore (Calbiochem‎)


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