Esta buscando: Phenylthiohydantoin-proline

Numero del catalogo: (USBIP9010-65A-HRP)

Proveedor: US Biological

Descripción: Anti-Proline Dehydrogenase Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

UOM: 1 * 200 µl

Promoción

Numero del catalogo: (USBIP9010-65A-BIOT)

Proveedor: US Biological

Descripción: Anti-Proline Dehydrogenase Rabbit Polyclonal Antibody (Biotin)

UOM: 1 * 200 µl

Promoción

Numero del catalogo: (BOSSBS-5813R-A488)

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

Promoción

Proveedor: TCI

Descripción: Hidrogeno-(S)-pirrolidina-1,2-dicarboxilato de 1-(terc-butilo) ≥99.0% (by titrimetric analysis)

Proveedor: Thermo Fisher Scientific

Descripción: (S)-Hidrogenopirrolidina-1,2-dicarboxilato de 1-(9H-fluoren-9-ilmetilo) ≥98%

FDS Certificados

Numero del catalogo: (BOSSBS-5813R-CY5.5)

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

Promoción

Numero del catalogo: (BOSSBS-5813R-CY3)

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

Promoción

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

Promoción

Proveedor: TCI

Descripción: Boc-L-Pro-OMe ≥97.0% (por GC)

Proveedor: Thermo Fisher Scientific

Descripción: Hidrogeno-(S)-pirrolidina-1,2-dicarboxilato de 1-(terc-butilo) ≥99%

FDS Certificados

Proveedor: TCI

Descripción: Captopril ≥98.0% (by HPLC, titration analysis)

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

Promoción

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

Promoción

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

Promoción

Numero del catalogo: (USBIP9010-65A-FITC)

Proveedor: US Biological

Descripción: Anti-Proline Dehydrogenase Rabbit Polyclonal Antibody (FITC (Fluorescein))

UOM: 1 * 200 µl

Promoción

Numero del catalogo: (A1705.0250)

Proveedor: PanReac AppliChem

Descripción: trans-4-Hidroxi-L(-)-prolina

UOM: 1 * 250 g

Promoción