Aminomethyltransferase anticorps

N° du produit ABIN2459732

L’anticorps Lapin Polyclonal anti-Aminomethyltransferase a été validé pour WB et ELISA. Il convient pour détecter Aminomethyltransferase dans des échantillons de Humain, Souris, Rat et Chien.

Aperçu rapide pour Aminomethyltransferase anticorps (ABIN2459732)

Antigène: Aminomethyltransferase (AMT)

Reactivité: Humain, Souris, Rat, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Aminomethyltransferase est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Aminomethyltransferase anticorps

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human AMT.

Information d'application

Indications d'application: AMT antibody can be used for detection of AMT by ELISA at 1:12500. AMT antibody can be used for detection of AMT by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store AMT antibody at -20 °C.

Détails sur Aminomethyltransferase

Antigène: Aminomethyltransferase (AMT)

Autre désignation: AMT

Sujet: The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 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). Glycine encephalopathy (GCE) may be due to a defect in any one of these enzymes.The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase, MIM 238300), H protein (a lipoic acid-containing protein, MIM 238330), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase, MIM 238331). Glycine encephalopathy (GCE, MIM 605899) may be due to a defect in any one of these enzymes.

Poids moléculaire: 44 kDa

ID gène: 275

NCBI Accession: NP_000472

UniProt: P48728