SLC39A5 Rabbit pAb, Cy3 conjugated(bs-19833R-Cy3)-100ul

SLC39A5 Rabbit pAb, Cy3 conjug

ated(bs-19833R-Cy3)-100ul
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  • ¥2980
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  • bs-19833R-Cy3
  • 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-19833R-Cy3
    英文名称SLC39A5 Rabbit pAb, Cy3 conjugated
    中文名称Cy3标记的溶质载体家族蛋白39成员A5抗体
    英文别名LZT Hs7; MGC34778; OTTHUMP00000211153; OTTHUMP00000211154; S39A5_HUMAN; SLC39A5; solute carrier family 39(metal ion transporter), member 5; Solute carrier family 39 member 5; Zinc transporter ZIP5 [Precursor]; Zinc transporter ZIP5; ZIP 5; ZIP-5; ZIP5; Zrt and Irt like protein 5; Zrt-and Irt-like protein 5.
    产品应用ICC/IF=1:50-200, 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 SLC39A5
    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

    Metabolism > Pathways and Processes > Cofactors, Vitamins / minerals > Vitamins / minerals

    Metabolism > Types of disease > Cancer

    Signal Transduction > Metabolism > Plasma Membrane > Channels

    Signal Transduction > Metabolism > Vitamins / Minerals

    亚细胞定位Basolateral cell membrane.
    组织特异性Expressed in liver, kidney, pancreas, small intestine, colon, spleen, fetal liver and fetal kidney.
    翻译后修饰Glycosylated.
    相似性Belongs to the ZIP transporter (TC 2.A.5) family.
    功能May play a role in polarized cells by carrying out serosal-to-mucosal zinc transport. Seems to play a central role in controlling organismal zinc status.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料The protein encoded by this gene belongs to the ZIP family of zinc transporters that transport zinc into cells from outside, and play a crucial role in controlling intracellular zinc levels. Zinc is an essential cofactor for many enzymes and proteins involved in gene transcription, growth, development and differentiation. Mutations in this gene have been associated with autosomal dominant high myopia (MYP24). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]

     

    应用推荐稀释比例
    {ICC/IF}{1:50-200}
    {IF}{1:100-500}

     

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