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5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin
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5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin
Artikel-Nr:
(BOSSBS-9521R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-A680
Lokale Artikelnummer::
BOSSBS-9521R-A680
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9521R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R
Lokale Artikelnummer::
BOSSBS-9521R
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9521R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-A647
Lokale Artikelnummer::
BOSSBS-9521R-A647
Beschreibung:
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.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
meso-Tetraphenylporphin 97%
Lieferant:
Alfa Aesar
Beschreibung:
meso-Tetraphenylporphin chlorarm
Lieferant:
Alfa Aesar
Beschreibung:
Zinc meso-tetraphenylporphine
Artikel-Nr:
(BOSSBS-9521R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-A350
Lokale Artikelnummer::
BOSSBS-9521R-A350
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9521R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-CY5.5
Lokale Artikelnummer::
BOSSBS-9521R-CY5.5
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9521R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-A488
Lokale Artikelnummer::
BOSSBS-9521R-A488
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9521R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-A750
Lokale Artikelnummer::
BOSSBS-9521R-A750
Beschreibung:
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.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Iron(III) meso-tetraphenylporphine chloride
Artikel-Nr:
(BOSSBS-7954R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7954R-A680
Lokale Artikelnummer::
BOSSBS-7954R-A680
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR918293-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR918293-1G
Lokale Artikelnummer::
APOSOR918293-1G
Beschreibung:
Chloride ionophore I 97%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-9521R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-HRP
Lokale Artikelnummer::
BOSSBS-9521R-HRP
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9521R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9521R-FITC
Lokale Artikelnummer::
BOSSBS-9521R-FITC
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7954R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7954R
Lokale Artikelnummer::
BOSSBS-7954R
Beschreibung:
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.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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