DL-\u03B1-Phenylalanin
Artikel-Nr:
(USBIF2965-10A)
Lieferant:
US Biological
Hersteller-Artikelnummer::
F2965-10A
Lokale Artikelnummer::
USBIF2965-10A
Beschreibung:
Anti-FARSB Mouse Monoclonal Antibody [clone: 2F11]
VE:
1 * 50 µG
Artikel-Nr:
(8.14599.0050)
Lieferant:
Merck
Hersteller-Artikelnummer::
8.14599.0050
Lokale Artikelnummer::
MERC8.14599.0050
Beschreibung:
N-Acetyl-DL-Valin zur Synthese, Sigma-Aldrich®
VE:
1 * 50 g
Artikel-Nr:
(USBI126631)
Lieferant:
US Biological
Hersteller-Artikelnummer::
126631
Lokale Artikelnummer::
USBI126631
Beschreibung:
Anti-FARS2 Mouse Monoclonal Antibody [clone: 3F1]
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-15472R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15472R-FITC
Lokale Artikelnummer::
BOSSBS-15472R-FITC
Beschreibung:
HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15472R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15472R
Lokale Artikelnummer::
BOSSBS-15472R
Beschreibung:
HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyze the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterized by urine that turns dark on standing and alkalinization, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15472R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15472R-HRP
Lokale Artikelnummer::
BOSSBS-15472R-HRP
Beschreibung:
HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
VE:
1 * 100 µl
Lieferant:
VWR Chemicals
Beschreibung:
DL-Natriumlactat 50% in wässriger Lösung Ph. Eur.
Artikel-Nr:
(BOSSBS-0136R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0136R-FITC
Lokale Artikelnummer::
BOSSBS-0136R-FITC
Beschreibung:
GTP cyclohydrolase I (also designated dopa-responsive dystonia) catalyzes the conversion of GTP to D-erythro-7,8-dihydroneopterin triphosphate, the first and rate-limiting step in tetrahydrobiopterin (BH4) biosynthesis. Tetrahydrobiopterin is an essential cofactor for 3 aromatic amino acid monooxygenases: phenylalanine, tyrosine, and tryptophan hydroxylases. Animals can synthesize tetrahydrobiopterin in vivo from GTP through several enzymatic reactions.
VE:
1 * 100 µl
Artikel-Nr:
(47786.)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
47786
Lokale Artikelnummer::
SUPL47786
Beschreibung:
DL-α-Tocopherolacetat
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-15472R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15472R-CY3
Lokale Artikelnummer::
BOSSBS-15472R-CY3
Beschreibung:
HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyse the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterised by urine that turns dark on standing and alkalinisation, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.
VE:
1 * 100 µl
Artikel-Nr:
(47783.)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
47783
Lokale Artikelnummer::
SUPL47783
Beschreibung:
DL-α-Tocopherol
VE:
1 * 1 ST
Artikel-Nr:
(22478.260)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC22478.260
Beschreibung:
DL-Kampfer, Tabletten, TECHNICAL, raffiniert
VE:
1 * 500 g
Artikel-Nr:
(BOSSBS-0136R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0136R-A488
Lokale Artikelnummer::
BOSSBS-0136R-A488
Beschreibung:
GTP cyclohydrolase I (also designated dopa-responsive dystonia) catalyzes the conversion of GTP to D-erythro-7,8-dihydroneopterin triphosphate, the first and rate-limiting step in tetrahydrobiopterin (BH4) biosynthesis. Tetrahydrobiopterin is an essential cofactor for 3 aromatic amino acid monooxygenases: phenylalanine, tyrosine, and tryptophan hydroxylases. Animals can synthesize tetrahydrobiopterin in vivo from GTP through several enzymatic reactions.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0136R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0136R-HRP
Lokale Artikelnummer::
BOSSBS-0136R-HRP
Beschreibung:
GTP cyclohydrolase I (also designated dopa-responsive dystonia) catalyzes the conversion of GTP to D-erythro-7,8-dihydroneopterin triphosphate, the first and rate-limiting step in tetrahydrobiopterin (BH4) biosynthesis. Tetrahydrobiopterin is an essential cofactor for 3 aromatic amino acid monooxygenases: phenylalanine, tyrosine, and tryptophan hydroxylases. Animals can synthesize tetrahydrobiopterin in vivo from GTP through several enzymatic reactions.
VE:
1 * 100 µl
Artikel-Nr:
(BTIUBNUM0812-50)
Lieferant:
Biotium
Hersteller-Artikelnummer::
BNUM0812-50
Lokale Artikelnummer::
BTIUBNUM0812-50
Beschreibung:
Recognizes a cluster of proteins between 70-80 kDa, identified as tyrosinase. Occasionally a minor band at 55 kDa is also detected. This MAb shows no cross-reaction with MAGE-1 and tyrosinase-related protein 1, TRP-1/gp75. Tyrosinase is a copper-containing metalloglycoprotein that catalyzes several steps in the melanin pigment biosynthetic pathway; the hydroxylation of tyrosine to L-3,4-dihydroxy-phenylalanine (dopa), and the subsequent oxidation of dopa to dopaquinone. Mutations of the tyrosinase gene occur in various forms of albinism. Tyrosinase is one of the targets for cytotoxic T-cell recognition in melanoma patients. Staining of melanomas with this MAb shows tyrosinase in melanotic as well as amelanotic variants. This MAb is a useful marker for melanocytes and melanomas.
VE:
1 * 50 µl
Preis auf Anfrage
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