FECH anticorps

N° du produit ABIN1385988

Détail du produit anti-FECH anticorps

Antigène: FECH (Ferrochelatase (FECH))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FECH est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human EPB41

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur FECH

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:

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