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RabbitAnti-MAT1A Rabbit pAb  antibody (bs-18691R)
~~~促销,代码KXJ230206~~~
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-18691R
英文名称 MAT1A Rabbit pAb
中文名称 腺苷蛋氨酸1抗体
别    名 AdoMet; Ams; MAT; MATA1; SAMS; SAMS1; SADE; SAS; METK1_HUMAN; MAT1A; AdoMet synthase 1; Methionine adenosyltransferase 1 (MAT 1); Methionine adenosyltransferase I/III (MAT-I/III); 2.5.1.6; AMS1; METK1_MOUSE; METK1_RAT;   
研究领域 细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 Mouse,  (predicted: Human, Rat, Cow, Horse, )
产品应用 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 44 kDa
细胞定位 细胞浆 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MAT1A: 231-330/395 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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.

SWISS:
Q00266

Gene ID:
610550

Database links:

Entrez Gene: 610550 Human

Entrez Gene: 11720 Mouse

Entrez Gene: 25331 Rat

Omim: 610550 Human

SwissProt: Q00266 Human

SwissProt: Q91X83 Mouse

SwissProt: P13444 Rat

Unigene: 282670 Human

Unigene: 14064 Mouse

Unigene: 10418 Rat



产品图片
Tissue/cell: mouse liver tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; Incubation: Anti-MAT1A Polyclonal Antibody, Unconjugated(bs-18691R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
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