Hľadali ste: 5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin

Dodávateľ: Thermo Fisher Scientific

Opis: 5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin 95%

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Dodávateľ: Apollo Scientific

Opis: 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin

Katalógové číslo: (ACRO292151000)

Dodávateľ: Thermo Fisher Scientific

Opis: Appearance: Violet to purple Crystalline powder

Merná jednotka: 1 * 100 mg

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Dodávateľ: CAYMAN

Opis: FeTPPS (Fe(III)5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato chloride) is a ferric porphyrin complex that causes the decomposition of peroxynitrite by catalytic isomerization to produce nitrate both<i> in vitro</i> and <i>in vivo</i>.

Dodávateľ: Apollo Scientific

Opis: meso-Tetra(4-carboxyphenyl)porphine 97%

Katalógové číslo: (89456-100MG-F)

Dodávateľ: Merck

Opis: Reagent for the spectrophotometric determination of ultra trace amounts of transition metals; determination by capillary zone electrophoresis.

Merná jednotka: 1 * 100 mg

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Dodávateľ: Apollo Scientific

Opis: 5,10,15,20-Tetra(4-pyridyl)porphyrin

Dodávateľ: ENZO LIFE SCIENCES

Opis: SOD mimetic. Peroxynitrite scavenger.

New Product

Dodávateľ: Thermo Fisher Scientific

Opis: Tetrasodium meso-tetra(sulphonatophenyl)porphine dodecahydrate ≥95%

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Katalógové číslo: (471370010.)

Dodávateľ: Thermo Fisher Scientific

Opis: Spiro-OMeTAD 98%

Merná jednotka: 1 * 1 g

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Katalógové číslo: (BOSSBS-9521R-CY7)

Dodávateľ: BIOSS INC

Opis: Ferrochelatase catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway, and is localised in the mitochondrion. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. Porphyrias are a group of inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). They are broadly classified as hepatic porphyrias or erythropoietic porphyrias, based on the site of the overproduction and mainly accumulation of the porphyrins (or their chemical precursors). They manifest with either skin problems, or neurological complications, or occasionally both.

Merná jednotka: 1 * 100 µl

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Katalógové číslo: (BOSSBS-9521R-CY5)

Dodávateľ: BIOSS INC

Opis: Ferrochelatase catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway, and is localised in the mitochondrion. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. Porphyrias are a group of inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). They are broadly classified as hepatic porphyrias or erythropoietic porphyrias, based on the site of the overproduction and mainly accumulation of the porphyrins (or their chemical precursors). They manifest with either skin problems, or neurological complications, or occasionally both.

Merná jednotka: 1 * 100 µl

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Katalógové číslo: (BOSSBS-9521R-CY3)

Dodávateľ: BIOSS INC

Opis: Ferrochelatase catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway, and is localised in the mitochondrion. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. Porphyrias are a group of inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). They are broadly classified as hepatic porphyrias or erythropoietic porphyrias, based on the site of the overproduction and mainly accumulation of the porphyrins (or their chemical precursors). They manifest with either skin problems, or neurological complications, or occasionally both.

Merná jednotka: 1 * 100 µl

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Katalógové číslo: (BOSSBS-9521R-A555)

Dodávateľ: BIOSS INC

Opis: Ferrochelatase catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway, and is localised in the mitochondrion. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. Porphyrias are a group of inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). They are broadly classified as hepatic porphyrias or erythropoietic porphyrias, based on the site of the overproduction and mainly accumulation of the porphyrins (or their chemical precursors). They manifest with either skin problems, or neurological complications, or occasionally both.

Merná jednotka: 1 * 100 µl

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Katalógové číslo: (ABCAAB146273-1)

Dodávateľ: ABCAM

Opis: Iron-containing porphyrin, used in a study to test in vitro activities of Rx-01 oxazolidinones against hospital and community pathogens.

Merná jednotka: 1 * 1 g

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Katalógové číslo: (BOSSBS-7954R-A750)

Dodávateľ: BIOSS INC

Opis: Catalyzes an early step in the biosynthesis of tetrapyrroles. Binds two molecules of 5-aminolevulinate per subunit, each at a distinct site, and catalyzes their condensation to form porphobilinogen.Involvement in disease:Defects in ALAD are the cause of acute hepatic porphyria (AHP). AHP is a form of porphyria. Porphyrias are inherited defects in the biosynthesis of heme, resulting in the accumulation and increased excretion of porphyrins or porphyrin precursors. They are classified as erythropoietic or hepatic, depending on whether the enzyme deficiency occurs in red blood cells or in the liver. AHP is characterized by attacks of gastrointestinal disturbances, abdominal colic, paralysis, and peripheral neuropathy. Most attacks are precipitated by drugs, alcohol, caloric deprivation, infections, or endocrine factors.

Merná jednotka: 1 * 100 µl

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