Hydroxyacyl-CoA Dehydrogenase (HADH) Peptide
HADH
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
N° du produit ABIN936175
382,12 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination:
France
Envoi sous 20 à 27 jours ouvrables
Aperçu rapide pour Hydroxyacyl-CoA Dehydrogenase (HADH) Peptide (ABIN936175)
Antigène
HADH
(Hydroxyacyl-CoA Dehydrogenase (HADH))
Origine
Mammifères
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
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Type de proteíne
- Synthetic
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Séquence
- YPMGPFELLD YVGLDTTKFI VDGWHEMDAE NPLHQPSPSL NKLVAENKFG
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Attributs du produit
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A synthetic peptide for use as a blocking control in assays to test for specificity of HADH antibody,
Alternative Names: HADH control peptide, HADH antibody Blocking Peptide, Anti-HADH Blocking Peptide, Hydroxyacyl-Coenzyme A Dehydrogenase Blocking Peptide, HAD Blocking Peptide, HADH1 Blocking Peptide, HADHSC Blocking Peptide, HHF4 Blocking Peptide, M/SCHAD Blocking Peptide, MGC8392 Blocking Peptide, SCHAD Blocking Peptide
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Indications d'application
- Optimal conditions should be determined by the investigator
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
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Buffer
- PBS
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Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20 °C long term.
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- HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))
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Sujet
- HADH functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene.
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Poids moléculaire
- 33 kDa
Antigène
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