PRODH anticorps (Center)
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- Antigène Voir toutes PRODH Anticorps
- PRODH (Proline Dehydrogenase (Oxidase) 1 (PRODH))
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Épitope
- Center
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp PRODH est non-conjugé
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Application
- Western Blotting (WB)
- Réactivité croisée
- Souris, Rat (Rattus), Boeuf (Vache)
- Réactivité croisée (Details)
- Mouse (84 %), Rat (83 %), Bovine (80 %)
- Attributs du produit
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Rabbit Polyclonal antibody to PRODH (proline dehydrogenase (oxidase) 1)
PRODH antibody [N1N3] - Purification
- Purified by antigen-affinity chromatography.
- Immunogène
- Recombinant protein encompassing a sequence within the center region of human PRODH. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product PRODH Anticorps primaire
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- Indications d'application
- Suggested dilution Reference Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceWestern blot1:500-1:3000*
- Commentaires
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Positive Control: 293T
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- 1XPBS, 1 % BSA, 20 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
- Agent conservateur
- Thimerosal (Merthiolate)
- Précaution d'utilisation
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Antigène
- PRODH (Proline Dehydrogenase (Oxidase) 1 (PRODH))
- Autre désignation
- PRODH (PRODH Produits)
- Sujet
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The protein encoded by this gene is a mitochondrial proline dehydrogenase that catalyzes the first step in proline degradation. Defects in this gene are a cause of hyperprolinemia type 1 and possibly susceptibility to schizophrenia 4 (SCZD4). The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes DiGeorge syndrome and CATCH22 syndrome.
Cellular Localization: Mitochondrion matrix - Poids moléculaire
- 68 kDa
- ID gène
- 5625
- Pathways
- Response to Water Deprivation, Monocarboxylic Acid Catabolic Process
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