FECH Antikörper (N-Term)
Kurzübersicht für FECH Antikörper (N-Term) (ABIN2777033)
Target
Alle FECH Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- N-Term
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Verwendungszweck
- FECH Antibody - N-terminal region
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Sequenz
- QHAQGAKPQV QPQKRYESNI RKPKTGILML NMGGPETLGD VHDFLLRLFL
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Homologie
- Human: 100%, Rat: 86%
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Produktmerkmale
- This is a rabbit polyclonal antibody against FECH. It was validated on Western Blot and immunohistochemistry.
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Aufreinigung
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the N terminal region of human FECH
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Applikationshinweise
- Optimal working dilution should be determined by the investigator.
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Kommentare
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under ABIN8100603
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handhabung
- prevent freeze-thaw cycles
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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
- 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.
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- FECH (Ferrochelatase (FECH))
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Andere Bezeichnung
- FECH
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Hintergrund
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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
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Molekulargewicht
- 48 kDa
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Gen-ID
- 2235
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NCBI Accession
- NP_001012533
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UniProt
- Q8NAN0
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Pathways
- Transition Metal Ion Homeostasis
Target
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