Recombinant人TRA2B protein (ab114393)

概述

描述

  • 性质Recombinant
  • 来源Escherichia coli
  • 氨基酸序列
    • AccessionP62995
    • 种属Human
    • 序列LGVFGLSLYTTERDLREVFSKYGPIADVSIVYDQQSRRSRGFAFVYFENV DDAKEAKERANGMELDGRRIRVDFSITKRP
    • 分子量34 kDa including tags
    • 氨基酸120 to 199

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技术指标

Our Abpromise guarantee covers the use of ab114393 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • 应用

    SDS-PAGE

    Western blot

    ELISA

  • 形式Liquid
  • 补充说明Protein concentration is above or equal to 0.05 mg/ml.
    ab114393 is best used within three months from the date of receipt.
  • Concentration information loading...

制备和贮存

  • 稳定性和存储

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.79% Tris citrate/phosphate, 0.3% Glutathione

常规信息

  • 别名
    • arginine/serine-rich 10
    • Arginine/serine-rich splicing factor 10
    • hTRA2-beta
    • SFRS10
    • Splicing factor
    • Splicing factor arginine/serine rich 10
    • SRFS10
    • TRA-2 beta
    • TRA2-beta
    • Tra2b
    • TRA2B_HUMAN
    • TRAN2B
    • Transformer 2 beta homolog
    • Transformer-2 protein homolog B
    • Transformer-2 protein homolog beta
    • Transformer-2-beta
    see all
  • 功能Sequence-specific RNA-binding protein which participates in the control of pre-mRNA splicing.
  • 组织特异性Highest expression in heart, skeletal muscle and pancreas. Less abundant in kidney, placenta and brain. Lowest expression in kidney and liver.
  • 序列相似性Belongs to the splicing factor SR family.
    Contains 1 RRM (RNA recognition motif) domain.
  • 翻译后修饰Phosphorylated in the RS domains.
    Dimethylation at Arg-241 is probably asymmetric.
  • 细胞定位Nucleus.
  • Information by UniProt

Recombinant Human TRA2B protein 图像

  • ab114393 analysed on a 12.5% SDS-PAGE Stained with Coomassie Blue.

Recombinant Human TRA2B protein (ab114393)参考文献

ab114393 has not yet been referenced specifically in any publications.

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