Methionine Adenosyltransferase I, alpha (MAT1A) Peptide
MAT1A
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all MAT1A products
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-MAT1A antibody (Catalog #: ARP41399_T100). 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
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 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.
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- 抗原
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
- 别名
- MAT Peptide, MATA1 Peptide, SAMS Peptide, SAMS1 Peptide, AdoMet Peptide, SADE Peptide, SAS Peptide, AI046368 Peptide, Ams Peptide, wu:fi35e01 Peptide, zgc:55442 Peptide, methionine adenosyltransferase 1A Peptide, methionine adenosyltransferase I, alpha Peptide, MAT1A Peptide, Mat1a Peptide, mat1a Peptide
- 背景
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MAT1A catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. MAT1A is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in its gene are associated with methionine adenosyltransferase deficiency.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.
Alias Symbols: MAT, MATA1, SAMS, SAMS1
Protein Size: 395 - 分子量
- 44 kDa
- 基因ID
- 4143
- NCBI登录号
- NM_000429, NP_000420
- UniProt
- Q00266
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