重组Brucella abortus Malate dehydrogenase蛋白(His tag) (ab224852)
Key features and details
- Expression system: Escherichia coli
- Purity: > 90% SDS-PAGE
- Tags: His tag N-Terminus
- Suitable for: SDS-PAGE, MS
描述
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产品名称
重组Brucella abortus Malate dehydrogenase蛋白(His tag) -
纯度
> 90 % SDS-PAGE. -
表达系统
Escherichia coli -
Accession
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蛋白长度
Full length protein -
无动物成分
No -
性质
Recombinant -
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种属
Brucella abortus -
序列
MARNKIALIGSGMIGGTLAHLAGLKELGDVVLFDIAEGTPQGKGLDIAES SPVDGFDAKFTGANDYAAIEGADVVIVTAGVPRKPGMSRDDLLGINLKVM EQVGAGIKKYAPEAFVICITNPLDAMVWALQKFSGLPAHKVVGMAGVLDS ARFRYFLSEEFNVSVEDVTVFVLGGHGDSMVPLARYSTVAGIPLPDLVKM GWTSQDKLDKIIQRTRDGGAEIVGLLKTGSAFYAPAASAIQMAESYLKDK KRVLPVAAQLSGQYGVKDMYVGVPTVIGANGVERIIEIDLDKDEKAQFDK SVASVAGLCEACIGIAPSLK -
预测分子量
54 kDa including tags -
氨基酸
1 to 320 -
标签
His tag N-Terminus -
额外的序列信息
Brucella abortus (strain S19) protein with a 10xHis-SUMO tag at the N-terminus and Myc tag at the C-terminus.
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相关产品
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Related Products
技术指标
Our Abpromise guarantee covers the use of ab224852 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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应用
SDS-PAGE
Mass Spectrometry
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质谱法
LC-MS/MS -
Concentration information loading...
制备和贮存
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稳定性和存储
Shipped at 4°C. Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 7.2
Constituents: 50% Glycerol (glycerin, glycerine), Tris buffer
常规信息
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别名
- mdh
图片
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Based on the SEQUEST from database of E.coli host and target protein, the LC-MS/MS analysis result of ab224852 could indicate that this peptide derived from E.coli-expressed Brucella abortus (strain S19) mdh.
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Based on the SEQUEST from database of E.coli host and target protein, the LC-MS/MS analysis result of ab224852 could indicate that this peptide derived from E.coli-expressed Brucella abortus (strain S19) mdh.
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
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SDS download
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Datasheet download
文献 (0)
ab224852 尚未被引用在任何文献中。