重组人MAP1D蛋白- BSA and Azide free (ab174389)
Key features and details
- Expression system: Escherichia coli
- Purity: > 85% SDS-PAGE
- Tags: His tag N-Terminus
- Suitable for: SDS-PAGE, MS
描述
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产品名称
重组人MAP1D蛋白- BSA and Azide free -
纯度
> 85 % 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 -
无载体
是 -
性质
Recombinant -
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种属
Human -
序列
MGSSHHHHHH SSGLVPRGSH MGSSSPLNHIYLHKQSSSQQRRNFFFRRQRDISHSIVLPAAVSSAHPVPK HIKKPDYVTTGIVPDWGDSIEVKNEDQIQGLHQACQLARHVLLLAGKSLK VDMTTEEIDALVHREIISHNAYPSPLGYGGFPKSVCTSVNNVLCHGIPDS RPLQDGDIINIDVTVYYNGYHGDTSETFLVGNVDECGKKLVEVARRCRDE AIAACRAGAPFSVIGNTISHITHQNGFQVCPHFVGHGIGSYFHGHPEIWH HANDSDLPMEEGMAFTIEPIITEGSPEFKVLEDAWTVVSLDNQRSAQFEH TVLITSRGAQILTKLPHEA -
预测分子量
37 kDa including tags -
氨基酸
20 to 335 -
标签
His tag N-Terminus -
额外的序列信息
(NP_954697.1)
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描述
重组人MAP1D蛋白(BSA and azide free)
技术指标
Our Abpromise guarantee covers the use of ab174389 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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形式
Liquid -
Concentration information loading...
制备和贮存
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稳定性和存储
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 8.00
Constituents: 20% Glycerol (glycerin, glycerine), 0.32% Tris-HCl buffer, 0.58% Sodium chloride, 0.02% DTT
常规信息
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别名
- AMP1D_HUMAN
- CDS of metAP 3 within PCR fragment
- M ethionine aminopeptidase 1D, mitochondrial precursor
see all -
功能
Removes the amino-terminal methionine from nascent proteins (By similarity). May play a role in colon tumorigenesis. -
组织特异性
Overexpressed in colon cancer cell lines and colon tumors as compared to normal tissues (at protein level). -
序列相似性
Belongs to the peptidase M24A family. -
细胞定位
Mitochondrion. - Information by UniProt
图片
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)
ab174389 尚未被引用在任何文献中。