Esta buscando: Protoporphyrin+IX

Proveedor: ENZO LIFE SCIENCES

Descripción: 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

Proveedor: SIGMA-ALDRICH MICROSCOPY

Descripción: Inhibits soluble guanylate cyclase.

Numero del catalogo: (ENZOALX430048M025)

Proveedor: ENZO LIFE SCIENCES

Descripción: Copper(II) protoporphyrin IX free acid

UOM: 1 * 25 mg

New Product Promoción

Numero del catalogo: (ENZOALX430076M025)

Proveedor: ENZO LIFE SCIENCES

Descripción: Heme oxygenase activator.

UOM: 1 * 25 mg

New Product Promoción

Proveedor: Thermo Scientific

Descripción: Zinc protoporphyrin ≥96%

MSDS Certificados

Proveedor: ENZO LIFE SCIENCES

Descripción: Potent inhibitor of heme oxygenase.

New Product

Proveedor: ENZO LIFE SCIENCES

Descripción: Potent and selective inhibitor of heme oxygenase (Ki=3nM), the enzyme that generates carbon monoxide (CO). Inhibits soluble guanylyl cyclase. Produces a time- and concentration-dependent inactivation of all three isoforms of nitric oxide synthase (IC50=0.8µM, 4.0µM, and 5.0µM for nNOS (NOS I), iNOS (NOS II) and eNOS (NOS III), respectively). Does not cross the blood-brain barrier. An useful tool to elucidate the role of CO in signal transduction and as a neurotransmitter.

New Product

Proveedor: Thermo Scientific

Descripción: Hemin derived from porcine is an iron-containing prosthetic group present in some proteins and can be an alternative source of iron within the host that contains a porphyrin ring containing a Fe2+ ion.
Hemin is a protoporphyrin IX containing a ferric iron (Fe3+) ion with a coordinating chloride ligand

MSDS

Numero del catalogo: (BOSSBS-9521R-CY5.5)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-9521R-A350)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-9521R-CY7)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-9521R-CY3)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-9521R-A555)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-9521R-CY5)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-9521R)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-9521R-A647)

Proveedor: Bioss

Descripción: 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

Promoción