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bs-103581P

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  • ¥980 - 2680
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  • bs-103581P
  • 2025年10月15日
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      20ug/50ug/100ug

    规格:20ug产品价格:¥980.0
    规格:50ug产品价格:¥1880.0
    规格:100ug产品价格:¥2680.0
    产品编号bs-103581P
    英文名称Recombinant Human G0S2 Protein, N-His-SUMO & C-Strep
    英文别名G0/G1 switch protein 2; G0/G1 switch regulatory protein 2; G0S2; Putative lymphocyte G0/G1 switch gene
    性状Lyophilized
    纯化方法AC
    理论分子量24.81 kDa
    储存液Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
    研究领域

    Cancer > Oncoproteins/suppressors > Oncoproteins

    亚基Directly interacts with BCL2; this interaction prevents the formation of the anti-apoptotic BAX-BCL2 complex.
    亚细胞定位Mitochondrion.
    组织特异性Widely expressed with highest levels in peripheral blood, skeletal muscle and heart, followed by kidney and liver.
    功能Potential oncogene and regulator of latent HIV.
    保存条件Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
    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G0S2 is a 103 amino acid novel target of peroxisome proliferator-activated receptors (PPARs) and regulator of latent HIV. G0S2 may be involved in adipocyte differentiation and its expression is essential for committing cells to enter the G1 phase of the cell cycle. G0S2 contains a CpG-rich island and multiple sites for potential phosphorylation by casein kinase II and protein kinase C. The gene encoding G0S2 maps to human chromosome 1, which is the largest human chromosome. Chromosome 1 spans about 260 million base pairs and makes up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

     

     

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