Betaine--Homocysteine S-Methyltransferase 2 (BHMT2) (Middle Region) Peptide
BHMT2
适用: 人
宿主: 合成
WB, BP
-
- 抗原 See all BHMT2 products
- BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))
- 蛋白结构域
- Middle Region
- 宿主
- 人
-
资源
- 合成
- 应用范围
- Western Blotting (WB), Blocking Peptide (BP)
- 序列
- GFVDLPEYPF GLESRVATRW DIQKYAREAY NLGVRYIGGC CGFEPYHIRA
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-BHMT2 Antibody(ARP48803_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
-
-
- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
-
- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
-
- 抗原
- BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))
- 别名
- C81077 Peptide, D13Ucla2 Peptide, BHMT2 Peptide, DKFZp469M1332 Peptide, bhmt-2 Peptide, betaine--homocysteine S-methyltransferase 2 Peptide, betaine-homocysteine methyltransferase 2 Peptide, betaine-homocysteine S-methyltransferase 2 Peptide, S-methylmethionine--homocysteine S-methyltransferase BHMT2 Peptide, BHMT2 Peptide, Bhmt2 Peptide, LOC100073266 Peptide
- 背景
-
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.
Alias Symbols: FLJ20001
Protein Size: 363 - 分子量
- 40 kDa
- 基因ID
- 23743
- NCBI登录号
- NM_017614, NP_060084
- UniProt
- Q9H2M3
-
You are here:
