BHMT2 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2715259

Détail du produit

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

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette BHMT2 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human BHMT2 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

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

Autre désignation: Bhmt2 (BHMT2 Produits)

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

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: 40.2 kDa

NCBI Accession: NP_060084

Pathways: Methionine Biosynthetic Process