HADH anticorps (AA 43-301)
Aperçu rapide pour HADH anticorps (AA 43-301) (ABIN7998630)
Antigène
Voir toutes HADH AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Classe de qualité
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Épitope
- AA 43-301
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Fonction
- Anti-HADH Antibody
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Réactivité croisée (Details)
- No cross reactivity with other proteins.
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Homologie
- Human HADH shares 90.3%,90.7% amino acid (aa) sequence identity with mouse,rat HADH,respectively.
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Attributs du produit
- Anti-HADH Antibody. Tested in ELISA, IF, IHC, ICC, WB, Flow Cytometry applications. This antibody reacts with Human, Mouse, Rat.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human HADH recombinant protein (Position: A43-K301). Human HADH shares 90.3% and 90.7% amino acid (aa) sequence identity with mouse and rat HADH, respectively.
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Isotype
- IgG
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Indications d'application
- Western blot, 0.1-0.25 μg/mL, Human, Mouse, Rat Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human, Rat Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human Immunofluorescence, 5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human ELISA, 0.1-0.5 μg/mL, -
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing. -
Date de péremption
- 12 months
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- HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))
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Autre désignation
- HADH
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Sujet
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Background: Hydroxyacyl-Coenzyme A dehydrogenase (HADH) is an enzyme which in humans is encoded by the HADH gene. 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 of this gene on chromosome 15.
Gene Full Name: hydroxyacyl-CoA dehydrogenase
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Poids moléculaire
- 34 kDa
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ID gène
- 3033
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UniProt
- Q16836
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Pathways
- Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process
Antigène
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