U heeft gezocht op: 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin

Catalogus nummer: (BOSSBS-9521R-A647)

Leverancier: Bioss

Omschrijving: 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.

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-9521R-A680)

Leverancier: Bioss

Omschrijving: Ferrochelatase catalyses 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.

UOM: 1 * 100 µl

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Catalogus nummer: (ABCAAB146273-1)

Leverancier: Abcam

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

UOM: 1 * 1 g

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Leverancier: ENZO LIFE SCIENCES

Omschrijving: Protoporphyrin IX free acid, as distinct from its zinc salt (which inhibits heme oxygenase), activates soluble guanylyl cyclase (sGC) by binding directly to the enzyme. A useful reagent in cases where the use of nitric oxide (NO) or nitric oxide donors is undesirable.

New Product

Catalogus nummer: (BOSSBS-9521R-CY5.5)

Leverancier: Bioss

Omschrijving: 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.

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-9521R-A350)

Leverancier: Bioss

Omschrijving: 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.

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-9521R-A488)

Leverancier: Bioss

Omschrijving: 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.

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-9521R-A750)

Leverancier: Bioss

Omschrijving: Ferrochelatase catalyses 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.

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-7954R-A680)

Leverancier: Bioss

Omschrijving: 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.

UOM: 1 * 100 µl

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Leverancier: Thermo Fisher Scientific

Omschrijving: meso-Tetraphenylporphine 97%

MSDS

Leverancier: Thermo Fisher Scientific

Omschrijving: meso-Tetraphenylporphine chlorine_low

MSDS Certificaten

Leverancier: Thermo Fisher Scientific

Omschrijving: Iron(III) meso-tetraphenylporphine chloride

MSDS Certificaten

Catalogus nummer: (TCIAT1359-1G)

Leverancier: TCI

Omschrijving: meso-Tetraphenylporphine 98,0 HPLC_ASSAY_METHOD chlorin_free

UOM: 1 * 1 g

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Catalogus nummer: (APOSOR11095-250MG)

Leverancier: Apollo Scientific

Omschrijving: meso-Tetraphenylporphine

UOM: 1 * 250 mg

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Leverancier: Thermo Fisher Scientific

Omschrijving: Zinc meso-tetraphenylporphine

MSDS Certificaten

Catalogus nummer: (APOSOR918293-1G)

Leverancier: Apollo Scientific

Omschrijving: Chloride ionophore I 97%

UOM: 1 * 1 g

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