You Searched For: 2-Amino-2-(4-pentoxyphenyl)acetic acid

Catalog Number: (BOSSBS-0136R-A350)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

Supplier: Spectrum Chemical

Description: L-Phenylalanine USP

Catalog Number: (USBI126629)

Supplier: US Biological

Description: Anti-FARS2 Mouse Polyclonal Antibody

UOM: 1 * 50 µG

Catalog Number: (BOSSBS-0136R-CY3)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-0136R)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

Supplier: Thermo Scientific

Description: CAS No.: 7524-50-7

MSDS

Catalog Number: (APOSOR322217-500G)

Supplier: APOLLO SCIENTIFIC

Description: (S)-Methyl-2-amino-3-phenylpropanoate hydrochloride 98%

UOM: 1 * 500 g

Catalog Number: (5202-100)

Supplier: Merck Millipore (Calbiochem‎)

Description: L-Phenylalanine, Millipore®

UOM: 1 * 100 g

Catalog Number: (BOSSBS-14371R-A750)

Supplier: Bioss

Description: DNAJB12 belongs to the evolutionarily conserved DNAJ/HSP40 family of proteins, which regulate molecular chaperone activity by stimulating ATPase activity. DNAJ proteins may have up to 3 distinct domains: a conserved 70-amino acid J domain, usually at the N terminus; a glycine/phenylalanine (G/F)-rich region; and a cysteine-rich domain containing 4 motifs resembling a zinc finger domain (Ohtsuka and Hata, 2000 [PubMed 11147971]).[supplied by OMIM, Mar 2008]

UOM: 1 * 100 µl

Catalog Number: (USBIF2965-10A)

Supplier: US Biological

Description: Anti-FARSB Mouse Monoclonal Antibody [clone: 2F11]

UOM: 1 * 50 µG

Catalog Number: (MOLE14133876-100G)

Supplier: Molekula

Description: L-Phenylalanine

UOM: 1 * 100 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (40870-25ML)

Supplier: Merck

Description: 3-Nitro-o-xylene, Supelco®

UOM: 1 * 25 mL

Catalog Number: (USBI126631)

Supplier: US Biological

Description: Anti-FARS2 Mouse Monoclonal Antibody [clone: 3F1]

UOM: 1 * 100 µG

Catalog Number: (BOSSBS-0136R-FITC)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

Catalog Number: (MOLEM31697582)

Supplier: Molekula

Description: DL-α-Phenylalanine

UOM: 1 * 100 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (BOSSBS-15472R)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl