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Image Unavailable-BOSSBS-13370R-A350

Anti-GLDC Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numero del catalogo: (BOSSBS-13370R-A350)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13370R-A680

Anti-GLDC Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numero del catalogo: (BOSSBS-13370R-A680)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13370R-A750

Anti-GLDC Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Numero del catalogo: (BOSSBS-13370R-A750)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13370R-HRP

Anti-GLDC Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numero del catalogo: (BOSSBS-13370R-HRP)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13370R-A488

Anti-GLDC Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numero del catalogo: (BOSSBS-13370R-A488)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13370R

Anti-GLDC Rabbit Polyclonal Antibody

Numero del catalogo: (BOSSBS-13370R)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13370R-A647

Anti-GLDC Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numero del catalogo: (BOSSBS-13370R-A647)
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.
UOM: 1 * 100 µl
Image Unavailable-648313-250

Tris-(hidroximetil) aminometano clorhidrato, Millipore®

Proveedor: Merck Millipore (Calbiochem‎)
Descripción: Tris-(hidroximetil) aminometano clorhidrato, Millipore®

Image Unavailable-ICNA04816116

Tris-(hidroximetil) aminometano clorhidrato ≥99%, white crystalline powder, grado ultrapuro

Proveedor: MP Biomedicals
Descripción: Solubility (5% aq soln) clear, colorless solution.

Image Unavailable-ICNA0520342901

Alizarina complexona

Numero del catalogo: (ICNA0520342901)
Proveedor: MP Biomedicals
Descripción: Alizarina complexona
UOM: 1 * 1 g
Image Unavailable-EHERC17894900

Tris-(hidroximetil) aminometano (TRIS, Trometamol)

Numero del catalogo: (EHERC17894900)
Proveedor: EHRENSTORFER
Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol)
UOM: 1 * 0,1 g
Image Unavailable-RC-105

Tris-(hidroximetil) aminometano (TRIS, Trometamol)

Numero del catalogo: (RC-105)
Proveedor: G-Biosciences
Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol)
UOM: 1 * 500 g
Image Unavailable-RC-108

Tris-(hidroximetil) aminometano clorhidrato

Proveedor: G-Biosciences
Descripción: Tris-(hidroximetil) aminometano clorhidrato

Image Unavailable-648317-100

Tris-(hidroximetil) aminometano clorhidrato, Millipore®

Proveedor: Merck Millipore (Calbiochem‎)
Descripción: Tris-(hidroximetil) aminometano clorhidrato, Millipore®

Certificados

Image Unavailable-1.08219.9012

Tris-(hidroximetil) aminometano clorhidrato, EMPROVE® EXPERT para producción biofarmacéutica, SAFC®

Proveedor: MERCK PRODUCTION CHEMICALS
Descripción: Tris-(hidroximetil) aminometano clorhidrato, EMPROVE® EXPERT para producción biofarmacéutica, SAFC®

FDS Certificados

Image Unavailable-648311-1

Tris-(hidroximetil) aminometano (TRIS, Trometamol), Millipore®

Proveedor: Merck Millipore (Calbiochem‎)
Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol), Millipore®

Consulta de precio
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta. Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta.
Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto ha sido bloqueado por su organización. Por favor, pónganse en contacto con su departamento de compras para obtener más información.
El producto original ya no está disponible. Su sustituto se muestra a continuación.
El producto(s) marcados con este símbolo están descatalogados - se venden hasta acabar stock. Pueden encontrar alternativas buscando con el número de catálogo VWR listado arriba. Si necesita más ayuda, por favor llame al Servicio de atención al cliente de VWR al 902.222.897.
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