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DUSP28 Antibody Blocking Pepti

de(bs-14460P)-500ug
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  • 2025年10月16日
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      500ug

    产品编号bs-14460P
    英文名称DUSP28 Antibody Blocking Peptide
    中文名称双特异性磷酸酶封闭多肽28封闭多肽
    英文别名Dual specificity phosphatase 28; DUSP28; DUS28_HUMAN; VHP.
    纯化方法HPLC
    研究领域

    Cell Biology > Apoptosis > Intracellular > Associated Proteins

    Cell Biology > Cell Cycle > Kinases/Phosphatases

    Signal Transduction > Protein Phosphorylation > Ser / Thr Kinases > MAPK Pathway

    亚基Monomer.
    亚细胞定位Cytoplasm. Nucleus.
    组织特异性Ubiquitous. Highest expression seen in heart, placenta, lung, liver, kidney and pancreas.
    翻译后修饰Myristoylation regulates subcellular location, and is necessary for activation of JNK.
    相似性Belongs to the protein-tyrosine phosphatase family. Non-receptor class dual specificity subfamily.
    Contains 1 tyrosine-protein phosphatase domain.
    功能DUSP28 belongs to the protein-tyrosine phosphatase family, non-receptor class dual specificity subfamily. It contains one tyrosine-protein phosphatase domain.
    保存条件Shipped at 4℃. Stored 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.
    背景资料Dual specificity phosphatases (DSPs) are a subclass of the protein tyrosine phosphatase (PTP) gene superfamily, which are selective for dephosphorylating critical phosphothreonine and phosphotyrosine residues within MAP kinases. DSP gene expression is induced by a host of growth factors and/or cellular stresses, thereby negatively regulating MAP kinase superfamily members. DUSP28 is a 176 amino acid protein that belongs to the protein-tyrosine phosphatase family and non-receptor class dual specificity subfamily. Containing one tyrosine-protein phosphatase domain, DUSP28 is encoded by a gene that maps to human chromosome 2, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2, including Harlequin icthyosis, sitosterolemia and Alstr鰉 syndrome.

     

     

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