D2HGDH anticorps (AA 322-521)

N° du produit ABIN7266669

Détail du produit anti-D2HGDH anticorps

Antigène: D2HGDH (D-2-Hydroxyglutarate Dehydrogenase (D2HGDH))

Épitope: AA 322-521

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp D2HGDH est non-conjugé

Application: Western Blotting (WB)

Fonction: D2HGDH Rabbit pAb

Séquence: GRHLHLASPV QESPFYVLIE TSGSNAGHDA EKLGHFLEHA LGSGLVTDGT MATDQRKVKM LWALRERITE ALSRDGYVYK YDLSLPVERL YDIVTDLRAR LGPHAKHVVG YGHLGDGNLH LNVTAEAFSP SLLAALEPHV YEWTAGQQGS VSAEHGVGFR KRDVLGYSKP PGALQLMQQL KALLDPKGIL NPYKTLPSQA

Réactivité croisée: Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 322-521 of human D2HGDH (NP_689996.4).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur D2HGDH

Antigène: D2HGDH (D-2-Hydroxyglutarate Dehydrogenase (D2HGDH))

Autre désignation: D2HGDH (D2HGDH Produits)

Synonymes: anticorps AA408776, anticorps AA408778, anticorps AI325464, anticorps RGD1307976, anticorps D2HGD, anticorps zgc:158661, anticorps D-2-hydroxyglutarate dehydrogenase, anticorps D2hgdh, anticorps D2HGDH, anticorps d2hgdh

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

Poids moléculaire: 32kDa/34kDa/56kDa

ID gène: 728294

UniProt: Q8N465