FECH antibody
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- Target See all FECH Antibodies
- FECH (Ferrochelatase (FECH))
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Reactivity
- Human, Mouse, Rat, Dog
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This FECH antibody is un-conjugated
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by protein A chromatography method.
- Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FECH.
- Top Product
- Discover our top product FECH Primary Antibody
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- Application Notes
- FECH antibody can be used for detection of FECH by ELISA at 1:1562500. FECH antibody can be used for detection of FECH by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Handling Advice
- As with any antibody avoid repeat freeze-thaw cycles.
- Storage
- 4 °C/-20 °C
- Storage Comment
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store FECH antibody at -20 °C.
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- Target
- FECH (Ferrochelatase (FECH))
- Alternative Name
- FECH (FECH Products)
- Synonyms
- AI894116 antibody, Fcl antibody, fch antibody, zgc:109851 antibody, EPP antibody, FCE antibody, CG2098 antibody, Dmel\\CG2098 antibody, GB15952 antibody, ferrochelatase L homeolog antibody, ferrochelatase antibody, Ferrochelatase antibody, ferrochelatase, mitochondrial antibody, ferrochelatase HemH antibody, ferrochelatase (predicted) antibody, fech.L antibody, hemH antibody, Fech antibody, FECH antibody, fech antibody, FeCH antibody, LOC409922 antibody, hem15 antibody, APH_RS01140 antibody
- Background
- 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.
- Molecular Weight
- 47 kDa, 48 kDa
- Gene ID
- 2235
- NCBI Accession
- NP_001012533
- UniProt
- Q8NAN0
- Pathways
- Transition Metal Ion Homeostasis
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