BHMT2 antibody
-
- Target See all BHMT2 Antibodies
- BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))
-
Reactivity
- Human, Mouse, Rat
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This BHMT2 antibody is un-conjugated
-
Application
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogen
- Fusion protein of human BHMT2
- Isotype
- IgG
- Top Product
- Discover our top product BHMT2 Primary Antibody
-
-
- Application Notes
- WB 1:1000-1:5000, IHC 1:30-1:150, ELISA 1:5000-1:10000
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- 0.78 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
-
- 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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
- Molecular Weight
-
Observed_MW: Refer to figures
Calculated_MW: 40 kDa
- UniProt
- Q9H2M3
- Pathways
- Methionine Biosynthetic Process
-