AAGAB Rabbit pAb, Biotin conjugated(bs-16102R-Bio)-100ul

AAGAB Rabbit pAb, Biotin conju

gated(bs-16102R-Bio)-100ul
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  • ￥2980
  • Bioss已认证
  • bs-16102R-Bio
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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北京博奥森生物技术有限公司
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    • 规格：

      100ul

    产品编号bs-16102R-Bio
    英文名称AAGAB Rabbit pAb, Biotin conjugated
    中文名称Biotin标记的AAGAB蛋白抗体
    英文别名FLJ11506; AAGAB_HUMAN; alpha and gamma adaptin binding protein p34; alpha-and gamma-adaptin-binding protein p34; LOC79719;
    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 AAGAB
    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

    Signal Transduction > Protein Trafficking > Vesicle Transport > Regulation

    亚基Associated with AP-1 and AP-2 complexes._x000D_
    亚细胞定位Cytoplasm, cytosol._x000D_
    组织特异性Widely expressed, including in skin and keratinocytes, with highest levels in adrenal gland, rectum and thymus.
    功能May play a role in membrane traffic.
    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Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FLJ11506 gene product has been provisionally designated FLJ11506 pending further characterization.

     

    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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