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Indole-3-carboxylic acid, 99%

HAA8370

Indole-3-carboxylic acid, 99%

CAS-NO

771-50-6

FORMULA

C9H7NO2

MOLECULAR WEIGHT

161,16 g/mole

ART-NO PRODUCT NAME QUANTITY PRICE  
HAA8370.010 Indole-3-carboxylic acid, 99% 10 g
€140.00
HAA8370.0025 Indole-3-carboxylic acid, 99% 25 g
€175.00
HAA8370.0100 Indole-3-carboxylic acid, 99% 100 g
€230.00
HAA8370.0250 Indole-3-carboxylic acid, 99% 250 g
€380.00

Further Information

Substrate for decarboxylase. The formation of indole can be detected by monitoring absorbance. Was used as chromogenic substrate for cloning genes encoding dioxygenases that act on aromatic acids. The p-cumate-degrading strain Pseudomonas putida F1 and the m- and p -toluate-degrading strain P. putida mt-2 transform indole-2-carboxylate and indole-3-carboxylate to colored products identified as indigo, indirubin, and isatin. Dioxygenase is thought to catalyse the first step in this reaction. 1. Eaton R.W., Chapman P.J., Formation of indigo and related compounds from indolecarboxylic acids by aromatic acid-degrading bacteria: chromogenic reactions for cloning genes encoding dioxygenases that act on aromatic acids. J. Bacteriol. 1995, 177, 6983-8. 2. Yoshida T., Fujita K., Nagasawa T., Novel reversible indole-3-carboxylate decarboxylase catalyzing nonoxidative decarboxylation. Biosci. Biotechnol. Biochem. 2002, 66, 2388-94.

Details

Substrate for decarboxylase. The formation of indole can be detected by monitoring absorbance. Was used as chromogenic substrate for cloning genes encoding dioxygenases that act on aromatic acids. The p-cumate-degrading strain Pseudomonas putida F1 and the m- and p -toluate-degrading strain P. putida mt-2 transform indole-2-carboxylate and indole-3-carboxylate to colored products identified as indigo, indirubin, and isatin. Dioxygenase is thought to catalyse the first step in this reaction. 1. Eaton R.W., Chapman P.J., Formation of indigo and related compounds from indolecarboxylic acids by aromatic acid-degrading bacteria: chromogenic reactions for cloning genes encoding dioxygenases that act on aromatic acids. J. Bacteriol. 1995, 177, 6983-8. 2. Yoshida T., Fujita K., Nagasawa T., Novel reversible indole-3-carboxylate decarboxylase catalyzing nonoxidative decarboxylation. Biosci. Biotechnol. Biochem. 2002, 66, 2388-94.

Additional Information

ART-NO HAA8370
CAS-NO 771-50-6
DETAIL NAME Indole-3-carboxylic acid, 99%
FORMULA C9H7NO2
MOLECULAR WEIGHT 161,16
Bezeichnung Mol Ge g/mole
QUANTITY 25 g
neu N

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