D2HGDH anticorps (AA 322-521)
Aperçu rapide pour D2HGDH anticorps (AA 322-521) (ABIN7266669)
Antigène
Voir toutes D2HGDH AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 322-521
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Fonction
- D2HGDH Rabbit pAb
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Séquence
- GRHLHLASPV QESPFYVLIE TSGSNAGHDA EKLGHFLEHA LGSGLVTDGT MATDQRKVKM LWALRERITE ALSRDGYVYK YDLSLPVERL YDIVTDLRAR LGPHAKHVVG YGHLGDGNLH LNVTAEAFSP SLLAALEPHV YEWTAGQQGS VSAEHGVGFR KRDVLGYSKP PGALQLMQQL KALLDPKGIL NPYKTLPSQA
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Réactivité croisée
- Souris, Rat
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Attributs du produit
- Polyclonal Antibodies
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Purification
- Affinity purification
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Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 322-521 of human D2HGDH (NP_689996.4).
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Isotype
- IgG
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Indications d'application
- WB,1:500 - 1:2000
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- D2HGDH (D-2-Hydroxyglutarate Dehydrogenase (D2HGDH))
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Autre désignation
- D2HGDH
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Sujet
- This gene encodes D-2hydroxyglutarate dehydrogenase, a mitochondrial enzyme belonging to the FAD-binding oxidoreductase/transferase type 4 family. This enzyme, which is most active in liver and kidney but also active in heart and brain, converts D-2-hydroxyglutarate to 2-ketoglutarate. Mutations in this gene are present in D-2-hydroxyglutaric aciduria, a rare recessive neurometabolic disorder causing developmental delay, epilepsy, hypotonia, and dysmorphic features.,D2HGDH,D2HGD,Signal Transduction,Endocrine & Metabolism,D2HGDH
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Poids moléculaire
- 32kDa/34kDa/56kDa
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ID gène
- 728294
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UniProt
- Q8N465
Antigène
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