You Searched For: Protoporphyrin+IX


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Catalog Number: (ABCAAB216021-100)
Supplier: Abcam
Description: Mouse monoclonal [CA9/781] to Carbonic Anhydrase 9/CA9.
UOM: 1 * 100 µG


Catalog Number: (USBIC1105-80A)
Supplier: US Biological
Description: Anti-CA9 Mouse Monoclonal Antibody (PE (Phycoerythrin)) [clone: 7H20]
UOM: 1 * 100 Tests


Catalog Number: (USBI125193)
Supplier: US Biological
Description: Anti-COL9A3 Rabbit Polyclonal Antibody
UOM: 1 * 100 µG


Catalog Number: (USBI125243)
Supplier: US Biological
Description: Anti-COX10 Mouse Polyclonal Antibody
UOM: 1 * 50 µG


Catalog Number: (ABCAAB212962-100)
Supplier: Abcam
Description: Mouse monoclonal [CA9/781] to Carbonic Anhydrase 9/CA9 - BSA and Azide free.
UOM: 1 * 100 µG


Catalog Number: (PRSI29-620)
Supplier: ProSci Inc.
Description: Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria.Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.
UOM: 1 * 100 µG


Catalog Number: (USBI034100-BIOTIN)
Supplier: US Biological
Description: Anti-COL9A3 Rabbit Polyclonal Antibody (Biotin)
UOM: 1 * 200 µl


Catalog Number: (PRSI29-655)
Supplier: ProSci Inc.
Description: Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria.Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.
UOM: 1 * 50 µG


Catalog Number: (1.09494.0100)
Supplier: Merck
Description: <B>Safety note: </B>These solutions are generally in acid solution.
UOM: 1 * 100 mL

Supplier: Thermo Fisher Scientific
Description: 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
Catalog Number: (APOSIN10658-100MG)
Supplier: Apollo Scientific
Description: Zinc Protoporphyrin 100mg pack 1 * 100 mg
UOM: 1 * 100 mg

New Product


Catalog Number: (APOSIN10658-250MG)
Supplier: Apollo Scientific
Description: Zinc Protoporphyrin 250mg pack 1 * 250 mg
UOM: 1 * 250 mg

New Product


Catalog Number: (USBI035312-BIOTIN)
Supplier: US Biological
Description: Anti-F9 Rabbit Polyclonal Antibody (Biotin)
UOM: 1 * 200 µl


Catalog Number: (BOSSBS-9521R)
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.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-9521R-A680)
Supplier: Bioss
Description: 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


Catalog Number: (BOSSBS-9521R-A647)
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.
UOM: 1 * 100 µl


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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