FECH anticorps (N-Term)

N° du produit ABIN2777033

L’anticorps anti-FECH Polyclonal Lapin est utilisé pour la détection de FECH dans des échantillons de Humain et Rat. Il a été validé pour WB et IHC.

Aperçu rapide pour FECH anticorps (N-Term) (ABIN2777033)

Antigène: FECH (Ferrochelatase (FECH))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FECH est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-FECH anticorps

Épitope: N-Term

Fonction: FECH Antibody - N-terminal region

Séquence: QHAQGAKPQV QPQKRYESNI RKPKTGILML NMGGPETLGD VHDFLLRLFL

Homologie: Human: 100%, Rat: 86%

Attributs du produit: This is a rabbit polyclonal antibody against FECH. It was validated on Western Blot and immunohistochemistry.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human FECH

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under ABIN8100603

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur FECH

Antigène: FECH (Ferrochelatase (FECH))

Autre désignation: FECH

Sujet:

Background Information: 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.

Gene Name: Ferrochelatase

Alternative Symbols: EPP, FCE, EPP1

Protein Name: Ferrochelatase, mitochondrial

Poids moléculaire: 48 kDa

ID gène: 2235

NCBI Accession: NP_001012533

UniProt: Q8NAN0

Pathways: Transition Metal Ion Homeostasis