BHMT2 anticorps

N° du produit ABIN7246028

Détail du produit anti-BHMT2 anticorps

Antigène: BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BHMT2 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Fusion protein of human BHMT2

Isotype: IgG

Information d'application

Indications d'application: WB 1:1000-1:5000, IHC 1:30-1:150, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.78 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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 BHMT2

Antigène: BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))

Autre désignation: BHMT2 (BHMT2 Produits)

Synonymes: anticorps C81077, anticorps D13Ucla2, anticorps BHMT2, anticorps DKFZp469M1332, anticorps bhmt-2, anticorps betaine--homocysteine S-methyltransferase 2, anticorps betaine-homocysteine methyltransferase 2, anticorps betaine-homocysteine S-methyltransferase 2, anticorps S-methylmethionine--homocysteine S-methyltransferase BHMT2, anticorps BHMT2, anticorps Bhmt2, anticorps LOC100073266

Sujet: Homocysteine is a sulfur-containing amino acid that plays a crucial role in methylation reactions. Transfer of the methyl group from betaine to homocysteine creates methionine, which donates the methyl group to methylate DNA, proteins, lipids, and other intracellular metabolites. The protein encoded by this gene is one of two methyl transferases that can catalyze the transfer of the methyl group from betaine to homocysteine. Anomalies in homocysteine metabolism have been implicated in disorders ranging from vascular disease to neural tube birth defects such as spina bifida. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire:

Observed_MW: Refer to figures

Calculated_MW: 40 kDa

UniProt: Q9H2M3

Pathways: Methionine Biosynthetic Process