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货号： bs-18691R-PE-Cy3 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-18691R-PE-Cy3
- 英文名称
- Anti-MAT1A/PE-Cy3
- 中文名称
- PE-Cy3标记的腺苷蛋氨酸1抗体
- 别 名
- AdoMet; AdoMet synthetase 1; AI046368; Ams; MAT; METK1_HUMAN; MAT I/III; MATA1; Methionine adenosyltransferase 1; Methionine adenosyltransferase I, alpha; Methionine adenosyltransferase I/III; MGC108563; S adenosylmethionine synthetase isoform type 1; SADE; SAMS; SAMS1.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 细胞生物 免疫学
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Cow, Horse,
- 产品应用
- ICC=1:50-200 IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 44kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human MAT1A
- 亚 型
- IgG
- 纯化方法
- affinity purified by Protein A
- 储 存 液
- 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
- 保存条件
- Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
- 产品介绍
- background:
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. Mutations in this gene are associated with methionine adenosyltransferase deficiency.
Function:
Catalyzes the formation of S-adenosylmethionine from methionine and ATP.
Subunit:
Homotetramer (MAT-I) or homodimer (MAT-III).
Tissue Specificity:
Expressed in liver.
Post-translational modifications:
S-nitrosylation of Cys-120 inactivates the enzyme.
DISEASE:
Methionine adenosyltransferase deficiency (MATD) [MIM:250850]: An inborn error of metabolism resulting in isolated hypermethioninemia. Most patients have no clinical abnormalities, although some neurologic symptoms may be present in rare cases with severe loss of methionine adenosyltransferase activity.Note: The disease is caused by mutations affecting the gene represented in this entry.
Similarity:
Belongs to the AdoMet synthase family.
Database links:Entrez Gene: 610550Human
Entrez Gene: 11720Mouse
Entrez Gene: 25331Rat
Omim: 610550Human
SwissProt: Q00266Human
SwissProt: Q91X83Mouse
SwissProt: P13444Rat
Unigene: 282670Human
Unigene: 14064Mouse
Unigene: 10418Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.