GLDC anticorps (AA 36-290)

N° du produit ABIN6141119

L’anticorps Lapin Polyclonal anti-GLDC a été validé pour WB, IHC, IP et IF. Il convient pour détecter GLDC dans des échantillons de Humain.

Aperçu rapide pour GLDC anticorps (AA 36-290) (ABIN6141119)

Antigène: GLDC (Glycine Dehydrogenase (GLDC))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GLDC est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), Immunofluorescence (IF)

Détail du produit anti-GLDC anticorps

Épitope: AA 36-290

Séquence: DSSSGGGDSA AAGASRLLER LLPRHDDFAR RHIGPGDKDQ REMLQTLGLA SIDELIEKTV PANIRLKRPL KMEDPVCENE ILATLHAISS KNQIWRSYIG MGYYNCSVPQ TILRNLLENS GWITQYTPYQ PEVSQGRLES LLNYQTMVCD ITGLDMANAS LLDEGTAAAE ALQLCYRHNK RRKFLVDPRC HPQTIAVVQT RAKYTGVLTE LKLPCEMDFS GKDVSGVLFQ YPDTEGKVED FTELVERAHQ SGSLA

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 36-290 of human GLDC (NP_000161.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:100,IF,1:50 - 1:100,IP,1:50 - 1:200

Commentaires:

HIGH QUALITY

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 GLDC

Antigène: GLDC (Glycine Dehydrogenase (GLDC))

Autre désignation: GLDC

Sujet: 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).,GLDC,GCE,GCSP,HYGN1,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,GLDC

Poids moléculaire: 112 kDa

ID gène: 2731

UniProt: P23378