You Searched For: 5,10,15,20-Tetrakis(4-carboxymethyloxyphenyl)porphyrin

Supplier: TCI America

Description: CAS Number: 16834-13-2
Molecular Formula: C40H26N8
Molecular Weight: 618.70
Purity/Analysis Method: >96.0% (N)
Form: Crystal
Color: Purple

Certificates

Supplier: Enzo Life Sciences

Description: SOD mimetic

Supplier: Thermo Scientific Chemicals

Description: Tetrasodium meso-tetra(sulfonatophenyl)porphine dodecahydrate ≥95%

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Catalog Number: (CA80051-608)

Supplier: MilliporeSigma

Description: Catalyzes the isomerization of peroxynitrite (ONOO-) to nitrate (NO3-) under physiological conditions and at realistic dose-derived concentrations (Kcat=2.2x106 M-1s-1)

Catalog Number: (CA80053-226)

Supplier: MilliporeSigma

Description: Cell-permeable superoxide dismutase (SOD) mimetic and peroxynitrite scavenger. Protects endothelial cells in a dose-dependent manner (EC50~40 µM) against paraquat (2 mM). Inhibits the oxidation of Dihydrorhodamine 123 by peroxynitrite, but does not scavenge nitric oxide (NO).

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Catalog Number: (CA80053-228)

Supplier: MilliporeSigma

Description: Cell-permeable superoxide dismutase (SOD) mimetic. Catalyzes the dismutation of O2- (rate constant ~4x107 M-1s-1) even in the presence of excess EDTA. Can substitute for SOD in mutants of E. coli lacking this enzyme. MnTMPyP acts in vivo as an NADPH/GSH:O2- oxidoreductase rather than as an SOD mimetic. Also an efficient peroxynitrite reductase when redox coupled with biological antioxidants.

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Catalog Number: (75846-306)

Supplier: Hardy Diagnostics

Description: ALA Disks™, delta-aminolevulinic acid, for the differentiation and speciation of Haemophilus spp., a porphyrin test.

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Supplier: TCI America

Description: Zinc(II) Tetraphenylporphyrin, Purity: >98.0%(HPLC), Cas number: 14074-80-7, Molecular Formula: C44H28N4Zn, Molecular Weight: 678.12, Synonyms: 5,10,15,20-Tetraphenyl-21H,23H-porphine Zinc(II), Zinc(II) TPP, Appearance: Crystal - Powder, Size: 1G

SDS

Catalog Number: (75788-594)

Supplier: Prosci

Description: Uroporphyrinogen-III Synthase is an enzyme which belongs to the uroporphyrinogen-III synthase family. Uroporphyrinogen-III Synthase is ubiquitous and it is involved in Porphyrin metabolism. Porphyrins act as cofactors for a multitude of enzymes that perform a variety of processes within the cell such as Methionine synthesis (Vitamin B12) or oxygen transport (Heme). Uroporphyrinogen-III Synthase can catalyze cyclization of the linear Tetrapyrrole, Hydroxymethylbilane, to the Macrocyclic Uroporphyrinogen III, the branch point for the various sub-pathways leading to the wide diversity of Porphyrins. Defects in Uroporphyrinogen-III Synthase are the cause of Congenital Erythropoietic Porphyria (CEP).

Catalog Number: (10473-616)

Supplier: Bioss

Description: 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.

Catalog Number: (10490-722)

Supplier: Bioss

Description: 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.

Catalog Number: (10490-704)

Supplier: Bioss

Description: 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.

Catalog Number: (10490-716)

Supplier: Bioss

Description: 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.

Catalog Number: (TCA5020-100MG)

Supplier: TCI America

Description: [Determination of Glucose in Serum and Urine]
CAS Number: 105250-49-5
MDL Number: MFCD00191476
Molecular Formula: C40H24N8OTi
Molecular Weight: 680.55
Purity/Analysis Method: >90.0% (HPLC)
Form: Crystal

SDS Certificates

Catalog Number: (10490-724)

Supplier: Bioss

Description: 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.

Catalog Number: (10490-718)

Supplier: Bioss

Description: 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.