Ferrochelatase (FECH) Peptide
FECH
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
-
- Antigène Tous les produits FECH
- FECH (Ferrochelatase (FECH))
- Type de proteíne
- Synthetic
- Origine
- Mammifères
-
Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Séquence
- LDRDLMTLPI QNKLAPFIAK RRTPKIQEQY RRIGGGSPIK IWTSKQGEGM
- Attributs du produit
-
A synthetic peptide for use as a blocking control in assays to test for specificity of FECH antibody,
Alternative Names: FECH control peptide, FECH antibody Blocking Peptide, Anti-FECH Blocking Peptide, Ferrochelatase Blocking Peptide, Protoporphyria Blocking Peptide, EPP Blocking Peptide, FCE Blocking Peptide
-
-
- Indications d'application
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
-
- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20 °C long term.
-
- Antigène
- FECH (Ferrochelatase (FECH))
- Synonymes
- AI894116 Peptide, Fcl Peptide, fch Peptide, zgc:109851 Peptide, EPP Peptide, FCE Peptide, CG2098 Peptide, Dmel\\CG2098 Peptide, GB15952 Peptide, ferrochelatase L homeolog Peptide, ferrochelatase Peptide, Ferrochelatase Peptide, ferrochelatase, mitochondrial Peptide, ferrochelatase HemH Peptide, ferrochelatase (predicted) Peptide, fech.L Peptide, hemH Peptide, Fech Peptide, FECH Peptide, fech Peptide, FeCH Peptide, LOC409922 Peptide, hem15 Peptide, APH_RS01140 Peptide
- Sujet
- 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.
- Poids moléculaire
- 47 kDa
-
Vous êtes ici:
