DMGDH anticorps (Middle Region)

N° du produit ABIN2789895

L’anticorps Lapin Polyclonal anti-DMGDH a été validé pour WB. Il convient pour détecter DMGDH dans des échantillons de Humain, Souris, Rat, Porc, Cheval, Lapin, Poisson zèbre (Danio rerio), Boeuf (Vache), Chien et Cobaye.

Aperçu rapide pour DMGDH anticorps (Middle Region) (ABIN2789895)

Antigène: DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Reactivité: Humain, Souris, Rat, Porc, Cheval, Lapin, Poisson zèbre (Danio rerio), Boeuf (Vache), Chien, Cobaye

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DMGDH est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-DMGDH anticorps

Épitope: Middle Region

Séquence: SELHDLRWIE EAAFRGGYDV EIQNITDEFG VLGVAGPYAR RVLQKLTSE

Homologie: Cow: 93%, Dog: 93%, Guinea Pig: 92%, Horse: 100%, Human: 100%, Mouse: 100%, Pig: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 83%

Attributs du produit: This is a rabbit polyclonal antibody against Dmgdh. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of mouse DMGDH

Information d'application

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeat freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur DMGDH

Antigène: DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Autre désignation: 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. Alternative splicing results in multiple transcript variants.
Alias Symbols: DMGDHD, ME2GLYDH
Protein Size: 869

Poids moléculaire: 93 kDa

ID gène: 29958

NCBI Accession: NM_013391, NP_037523

UniProt: Q9UI17