C1orf84 Rabbit pAb, Biotin conjugated(bs-16973R-Bio)-100ul

C1orf84 Rabbit pAb, Biotin con

jugated(bs-16973R-Bio)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-16973R-Bio
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-16973R-Bio
    英文名称C1orf84 Rabbit pAb, Biotin conjugated
    中文名称Biotin标记的1号染色体开放阅读框84抗体
    英文别名KIAA0467; Chromosome 1 open reading frame 84; FLJ34502; Hypothetical protein LOC23334; Protein SZT2; RP11-506B15.1; Seizure threshold 2 homolog A; Seizure threshold 2 protein homolog; SZT2; SZT2_HUMAN; SZT2A; Uncharacterized protein KIAA0467.
    产品应用IHC-P=1:100-500, IHC-F=1:100-500, IF=1:100-500

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human C1orf84
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Cell Biology > Other Antibodies > Other Antibodies

    亚细胞定位Peroxisome (By similarity).
    组织特异性Expressed in the brain, predominantly in the parietal and frontal cortex as well as in dorsal root ganglia.
    功能Involved in oxidative stress. May be involved in superoxide dismutase activity and in neuroprotective effect of peroxisomes, but has no direct dismutase activity when tested in yeast. May enhance epileptogenesis and confer low seizure threshold (By similarity).
    保存条件Shipped at 4℃. Store at -20°C 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SZT2 (seizure threshold 2 homolog (mouse)), also known as SZT2A or SZT2B, is a 3,432 amino acid peroxisomal protein that plays a role in resistance to oxidative stress. Predominantly expressed in the parietal and frontal cortex, as well as in dorsal root ganglia of the brain, SZT2 is implicated in superoxide dismutase activity and the neuroprotection in peroxisomes. Existing as four alternatively spliced isoforms, SZT2 is thought to enhance epileptogenesis and is encoded by a gene that maps to human chromosome 1p34.2. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes, comprises nearly 8% of the human genome and houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome.

     

    应用推荐稀释比例
    {IHC-P}{1:100-500}
    {IHC-F}{1:100-500}
    {IF}{1:100-500}

     

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