DMGDH anticorps (C-Term)

N° du produit ABIN1537626

Détail du produit anti-DMGDH anticorps

Antigène: DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Épitope: AA 836-864, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DMGDH est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This DMGDH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 836-864 amino acids from the C-terminal region of human DMGDH.

Clone: RB23867

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: DMGDH Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur DMGDH

Antigène: DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Autre désignation: DMGDH (DMGDH Produits)

Synonymes: anticorps MGC132281, anticorps DMGDHD, anticorps ME2GLYDH, anticorps Me2GlyDH, anticorps 1200014D15Rik, anticorps AI787269, anticorps dimethylglycine dehydrogenase, anticorps dimethylglycine dehydrogenase L homeolog, anticorps D-amino-acid oxidase, anticorps Dimethylglycine dehydrogenase, anticorps glycine cleavage system protein T, anticorps dimethylglycine dehydrogenase precursor, anticorps DMGDH, anticorps dmgdh.L, anticorps dmgdh, anticorps SAR11_1253, anticorps EAMY_RS27375, anticorps EAMY_RS33570, anticorps VDBG_06516, anticorps Sinme_2570, anticorps HALXA_RS03495, anticorps Dmgdh

Sujet: This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum.

Poids moléculaire: 96811

ID gène: 29958

NCBI Accession: NP_037523

UniProt: Q9UI17