You Searched For: 3-Nitrophenol

Catalog Number: (MOLE58558107-100G)

Supplier: Molekula

Description: 4-Nitro-m-cresol

UOM: 1 * 100 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (MOLEM69284514)

Supplier: Molekula

Description: 6-Nitro-m-cresol

UOM: 1 * 100 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (MOLEM46352676)

Supplier: Molekula

Description: 5-Nitro-o-cresol

UOM: 1 * 25 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (MOLE52961516-25G)

Supplier: Molekula

Description: 3-Nitro-p-cresol

UOM: 1 * 25 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (MOLE37682624-5G)

Supplier: Molekula

Description: 3-Nitro-o-cresol

UOM: 1 * 5 g

 This is a MarketSource item. Additional charges may apply

Supplier: MP Biomedicals

Description: Inhibitors: p-Chloromercuribenzoate, iodoacetamide, heavy metal ions (Zn²⁺, Fe²⁺, Zn²⁺, Cd²⁺, Cu²⁺, Pb²⁺, Ag⁺, Hg²⁺), ionic Detergents (SDS, DAC, etc.). Contaminants: The preparation is practically free from other glycosidases (a-galactosidase, a-,b-glucosidase, a-,b-mannosidase, etc.) and proteinase. Principle: o-Nitrophenyl-b-D-galactopyranoside (ONPG) b-galactosidase > o-Nitrophenol (ONP) + D-Galactose. The appearance of o-nitrophenol is measured at 410 nm by spectrophotemetry. Thermal Stability: Below 50 °C (pH 7,3; 15 min) (Lit.), Optimum Temperature: 50 to 55 °C (Lit.).

Supplier: MP Biomedicals

Description: One unit will hydrolyse 1,0 µmole of o-nitrophenyl-beta-D-galactoside to o-nitrophenol per minute at pH 4,5 and 30 °C.

Catalog Number: (MOLEM54449852)

Supplier: Molekula

Description: 3-Nitro-o-cresol

UOM: 1 * 5 g

 This is a MarketSource item. Additional charges may apply

Supplier: MP Biomedicals

Description: Inhibitors: p-Chloromercuribenzoate, lodoacetamide, heavy metal ions (Zn²⁺, Fe²⁺, Zn²⁺, Cd²⁺, Cu²⁺, Pb²⁺, Ag⁺, Hg²⁺), Ionic Detergents (SDS, DAC, etc.). Contaminants: The preparation is practically free from other glycosidases (a-galactosidase, a-,b-glucosidase, a-,b-mannosidase, etc.) and proteinase. Principle: o-Nitrophenyl-b-D-galactopyranoside (ONPG) b-galactosidase > <i>o</i>-Nitrophenol (ONP) +D-Galactose. The appearance of o-nitrophenol is measured at 410 nm by spectrophotemetry. Thermal stability: below 50 °C (pH 7,3; 15 min) (Lit.), Optimum Temperature: 50 to 55 °C (Lit.).

Catalog Number: (PRSI26-332)

Supplier: ProSci Inc.

Description: Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene sulfates dehydroepiandrosterone but not 4-nitrophenol, a typical substrate for the phenol and estrogen sulfotransferase subfamilies.Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene sulfates dehydroepiandrosterone but not 4-nitrophenol, a typical substrate for the phenol and estrogen sulfotransferase subfamilies. Two alternatively spliced variants that encode different isoforms have been described.

UOM: 1 * 50 µG

Catalog Number: (PRSI26-339)

Supplier: ProSci Inc.

Description: SULT1C4 catalyzes the sulfate conjugation of many drugs, xenobiotic compounds, hormones, and neurotransmitters. It may be involved in the activation of carcinogenic hyroxylamines. SULT1C4 shows activity towards p-nitrophenol and N-hydroxy-2-acetylamino-fluorene (N-OH-2AAF).Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a protein that belongs to the SULT1 subfamily, responsible for transferring a sulfo moiety from PAPS to phenol-containing compounds.

UOM: 1 * 50 µG

Catalog Number: (PRSI92-500)

Supplier: ProSci Inc.

Description: Human Sulfotransferase (SULT1C4) is an enzyme that in humans is encoded by the SULT1C4 gene, belongs to the sulfotransferase 1 family. SULT1C4 is expressed at high levels in fetal lung and kidney and at low levels in fetal heart, adult kidney, ovary and spinal chord. Sulfotransferase utilises 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyse the sulfate conjugation of drugs, xenobiotic compounds, hormones, and neurotransmitters. It shows activity towards p-nitrophenol and N-hydroxy-2-acetylamino-fluorene (N-OH-2AAF). SULT1C4 plays an important role incatalyzing the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds.

UOM: 1 * 50 µG

Supplier: MP Biomedicals

Description: p nitrophenol is the substrate of choice for use with alkaline phosphatase in ELISA procedures. This substrate produces a soluble end product that is yellow in color and can be read spectrophotometrically at 405 nm. The pNPP reaction may be stopped with 3 M NaOH and read at 405 nm.

MSDS

Catalog Number: (APOSOR72139-1G)

Supplier: APOLLO SCIENTIFIC

Description: 5-BROMO-3-METHOXY-2-NITROPHENOL 1 * 1 g

UOM: 1 * 1 g

Catalog Number: (APOSOR90455-5G)

Supplier: APOLLO SCIENTIFIC

Description: 4-BROMO-3-METHYL-2-NITROPHENOL 1 * 5 g

UOM: 1 * 5 g

New Product

Catalog Number: (APOSOR90620-5G)

Supplier: APOLLO SCIENTIFIC

Description: 4-BROMO-2-METHYL-6-NITROPHENOL 1 * 5 g

UOM: 1 * 5 g

New Product