GLDC anticorps (AA 574-1020)

N° du produit ABIN7875823

Cet anticorps anti-GLDC Monoclonal Souris (Clone 3D3D3) (ABIN7875823) détecte spécifiquement GLDC dans WB et IHC (p). L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour GLDC anticorps (AA 574-1020) (ABIN7875823)

Antigène: GLDC (Glycine Dehydrogenase (GLDC))

Reactivité: Humain, Souris, Rat

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp GLDC est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: 3D3D3

Détail du produit anti-GLDC anticorps

Épitope: AA 574-1020

Fonction: GLDC Antibody / Glycine Decarboxylase

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids K574-S1020) was used as the immunogen for the GLDC antibody.

Isotype: IgG1

Information d'application

Indications d'application: Optimal dilution of the GLDC antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the GLDC antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur GLDC

Antigène: GLDC (Glycine Dehydrogenase (GLDC))

Autre désignation: GLDC

Sujet: Glycine decarboxylase also known as glycine cleavage system P protein or glycine dehydrogenase is an enzyme that in humans is encoded by the GLDC gene. Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).

UniProt: P23378