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4\'-Acetylbiphenyl-3-carbonsäure
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4\'-Acetylbiphenyl-3-carbonsäure
Artikel-Nr:
(BOSSBS-5813R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-FITC
Lokale Artikelnummer::
BOSSBS-5813R-FITC
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A750
Lokale Artikelnummer::
BOSSBS-5813R-A750
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A680
Lokale Artikelnummer::
BOSSBS-5813R-A680
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A647
Lokale Artikelnummer::
BOSSBS-5813R-A647
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A555
Lokale Artikelnummer::
BOSSBS-5813R-A555
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A350
Lokale Artikelnummer::
BOSSBS-5813R-A350
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-CY5
Lokale Artikelnummer::
BOSSBS-5813R-CY5
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-CY3
Lokale Artikelnummer::
BOSSBS-5813R-CY3
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-CY5.5
Lokale Artikelnummer::
BOSSBS-5813R-CY5.5
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-HRP
Lokale Artikelnummer::
BOSSBS-5813R-HRP
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A488
Lokale Artikelnummer::
BOSSBS-5813R-A488
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(A1705.0250)
Lieferant:
PanReac AppliChem
Hersteller-Artikelnummer::
A1705.0250
Lokale Artikelnummer::
APLIA1705.0250
Beschreibung:
trans-4-Hydroxy-L(-)-prolin
VE:
1 * 250 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
trans-4-Hydroxy-L(-)-prolin
Artikel-Nr:
(181-1150)
Lieferant:
VACUUBRAND
Hersteller-Artikelnummer::
20696921
Lokale Artikelnummer::
VACU20696921
Beschreibung:
<B>Chemistry diaphragm pumps: </B>Chemistry diaphragm pumps in equipment category 2 (e.g. for Zone 1) with ATEX compliance. These pumps are exceptionally well designed for the avoidance of ignition sources. They have good chemical resistance, are oil-free, have no friction surfaces and the suction chamber is hermetically sealed off from the drive unit compartment. Motor with flameproof enclosure and integrated, self contained overcurrent and overheating protection for direct 230 V/60 Hz single-phase connection. Diaphragm pump heads made of anti-static materials. Chemically resistant: Materials in contact with media; fluorinated plastics, stainless steel, FFKM. Gas ballast with separate inert gas connection. Pressure relief valves inside and at the outlet. Safety membrane technology with the option for inert gas flushing and membrane tear detection.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-4225R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4225R-A647
Lokale Artikelnummer::
BOSSBS-4225R-A647
Beschreibung:
The UDP-Glucuronosyltransferases (UGT) comprise a family of enzymes that detoxify and enhance the urinary excretion of a wide variety of xenobiotic and endogenous substrates by transferring glucuronic acid to sulfhydryl, hydroxyl, aromatic amino, or carboxylic acid groups. They have been subdivided into two families, UGT1 and UGT2, based on the evolutionary divergence of their genes. The enzymes of the UGT1A family play an important role in the metabolism of dietary constituents, phenols, and therapeutic drugs, and also the glucuronidation of bilirubin and iodothyronines. The enzymes of the UGT2B family are involved in the metabolism of bile acids, phenol derivatives, catecholestrogens and steroids. Although it is widely recognized that the liver is the major site of glucuronidation, it is now clear that UGT enzymes are also found in extra-hepatic tissues.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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