VAT1L Rabbit pAb, BF594 conjugated(bs-8420R-BF594)-100ul

VAT1L Rabbit pAb, BF594 conjug

ated(bs-8420R-BF594)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-8420R-BF594
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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    • 规格

      100ul

    产品编号bs-8420R-BF594
    英文名称VAT1L Rabbit pAb, BF594 conjugated
    中文名称BF594标记的囊泡胺转运蛋白1家族蛋白抗体
    英文别名VAT1L_HUMAN; Synaptic vesicle membrane protein VAT-1 homolog-like; EC:1.-.-.-; KIAA1576; vesicle amine transport 1 like;
    产品应用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 KIAA1576/VAT1L
    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 > Oxidative Stress

    Metabolism > Pathways and Processes > Redox metabolism > Oxidative stress

    相似性Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.

     

    应用推荐稀释比例
    {IF}{1:100-500}

     

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