Esta buscando: Metanolato de t\u00E1ntalo(V)


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Numero del catalogo: (BOSSBS-5813R-A647)
Proveedor: Bioss
Descripción: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-5813R-HRP)
Proveedor: Bioss
Descripción: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-5813R-FITC)
Proveedor: Bioss
Descripción: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-5813R-A750)
Proveedor: Bioss
Descripción: Proline oxidase catalyses the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterised by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-5813R-A680)
Proveedor: Bioss
Descripción: Proline oxidase catalyses the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterised by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Numero del catalogo: (USBI040706-APC)
Proveedor: US Biological
Descripción: Anti-PYCR1 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
UOM: 1 * 200 µl


Numero del catalogo: (PRSI56-080)
Proveedor: ProSci Inc.
Descripción: PYCR2 belongs to the pyrroline-5-carboxylate reductase family. Pyrroline-5-carboxylate reductase catalyzes the the NAD(P)H-dependent conversion of proline to pyrroline-5-carboxylate.
UOM: 1 * 400 µl

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Numero del catalogo: (BOSSBS-5813R-CY5)
Proveedor: Bioss
Descripción: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Numero del catalogo: (ABNOMAB6588)
Proveedor: Abnova
Descripción: Mouse monoclonal antibody raised against pyrroline.
UOM: 1 * 20 µG


Numero del catalogo: (ABNOMAB6589)
Proveedor: Abnova
Descripción: Mouse monoclonal antibody raised against pyrroline.
UOM: 1 * 20 µG


Numero del catalogo: (PRSI30-099)
Proveedor: ProSci Inc.
Descripción: ALDH4A1 belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline.
UOM: 1 * 100 µG


Numero del catalogo: (PRSI30-100)
Proveedor: ProSci Inc.
Descripción: ALDH4A1 belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline.This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Two transcript variants encoding the same protein have been identified for this gene.
UOM: 1 * 100 µG


Proveedor: Apollo Scientific
Descripción: Benzyl Morpholinoacetate

Numero del catalogo: (APOSOR5145-1G)
Proveedor: Apollo Scientific
Descripción: 1-Benzyl-3-phenylpiperazine
UOM: 1 * 1 g


Numero del catalogo: (APOSOR470632-1G)
Proveedor: Apollo Scientific
Descripción: 2-Benzyl-3-hydroxypropanenitrile
UOM: 1 * 1 g


Proveedor: Apollo Scientific
Descripción: (R)-(+)-N-Benzyl-α-methylbenzylamine 98%

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