FECH anticorps (AbBy Fluor® 488)
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- Antigène Voir toutes FECH Anticorps
- FECH (Ferrochelatase (FECH))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp FECH est conjugé à/à la AbBy Fluor® 488
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human EPB41
- Isotype
- IgG
- Top Product
- Discover our top product FECH Anticorps primaire
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- Indications d'application
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- FECH (Ferrochelatase (FECH))
- Autre désignation
- FECH (FECH Produits)
- Synonymes
- anticorps AI894116, anticorps Fcl, anticorps fch, anticorps zgc:109851, anticorps EPP, anticorps FCE, anticorps CG2098, anticorps Dmel\\CG2098, anticorps GB15952, anticorps ferrochelatase L homeolog, anticorps ferrochelatase, anticorps Ferrochelatase, anticorps ferrochelatase, mitochondrial, anticorps ferrochelatase HemH, anticorps ferrochelatase (predicted), anticorps fech.L, anticorps hemH, anticorps Fech, anticorps FECH, anticorps fech, anticorps FeCH, anticorps LOC409922, anticorps hem15, anticorps APH_RS01140
- Sujet
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Synonyms: EPP, FCE, Ferrochelatase protoporphyria, Ferrochelatase, Ferrochelatase mitochondrial, Heme synthetase, Protoheme ferro lyase, HEMH_HUMAN.
Background: 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.
- ID gène
- 2235
- Pathways
- Transition Metal Ion Homeostasis
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