BHMT2 antibody (AA 1-347)

Catalog No. ABIN1885911

Product Details anti-BHMT2 Antibody

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

Binding Specificity: AA 1-347

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BHMT2 antibody is un-conjugated

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

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 347 of Human BHMT2

Application Details

Application Notes: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.500

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: Biohazard Informations: This product contains thimerosal which is hazardous.

Storage: 4 °C/-20 °C

Storage Comment: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Target Details for BHMT2

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

Alternative Name: BHMT2 (BHMT2 Products)

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

Background: 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.[provided by RefSeq]

Molecular Weight: 40 kDa

Gene ID: 23743

NCBI Accession: NP_060084, NM_017614

Pathways: Methionine Biosynthetic Process