C19orf48 Rabbit pAb, AE conjugated(bs-13785R-AE)-100ul

C19orf48 Rabbit pAb, AE conjug

ated(bs-13785R-AE)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-13785R-AE
  • 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-13785R-AE
    英文名称C19orf48 Rabbit pAb, AE conjugated
    中文名称AE标记的19号染色体开放阅读框48抗体
    英文别名C19orf48; CS048_HUMAN; Multidrug resistance-related protein; Uncharacterized protein C19orf48; Multidrug resistance-related protein, isoform CRA_a; MGC13170; hCG_2008493;
    产品应用ELISA=1:500-5000

    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 C19orf48
    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

    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf48 gene product has been provisionally designated C19orf48 pending further characterization.

     

    应用推荐稀释比例
    {ELISA}{1:500-5000}

     

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