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bs-106459P

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  • 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-106459P
    英文名称Recombinant Mouse OGG1 Protein, N-His
    英文别名N-glycosylase/DNA lyase; 8-oxoguanine DNA glycosylase; 3.2.2.-; DNA-(apurinic or apyrimidinic site) lyase; AP lyase; 4.2.99.18; Ogg1
    性状Lyophilized
    纯化方法AC
    理论分子量37.65 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 > Tumor biomarkers

    Epigenetics and Nuclear Signaling > DNA / RNA > DNA Damage & Repair > Base Excision Repair

    亚细胞定位Mitochondrion; Nucleus and Nucleus > nucleoplasm. Nucleus speckle. Nucleus matrix. Together with APEX1 is recruited to nuclear speckles in UVA-irradiated cells.
    组织特异性Ubiquitous.
    相似性Belongs to the type-1 OGG1 family.
    功能DNA repair enzyme that incises DNA at 8-oxoG residues. Excises 7,8-dihydro-8-oxoguanine and 2,6-diamino-4-hydroxy-5-N-methylformamidopyrimidine (FAPY) from damaged DNA. Has a beta-lyase activity that nicks DNA 3' to the lesion.
    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This gene encodes the enzyme responsible for the excision of 8-oxoguanine, a mutagenic base byproduct which occurs as a result of exposure to reactive oxygen. The action of this enzyme includes lyase activity for chain cleavage. Alternative splicing of the C-terminal region of this gene classifies splice variants into two major groups, type 1 and type 2, depending on the last exon of the sequence. Type 1 alternative splice variants end with exon 7 and type 2 end with exon 8. All variants share the N-terminal region in common, which contains a mitochondrial targeting signal that is essential for mitochondrial localization. Many alternative splice variants for this gene have been described, but the full-length nature for every variant has not been determined. [provided by RefSeq, Aug 2008].

     

     

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