TMEM158 Rabbit pAb, PE-Cy5.5 conjugated(bs-11770R-PE-Cy5.5)-100ul

TMEM158 Rabbit pAb, PE-Cy5.5 c

onjugated(bs-11770R-PE-Cy5.5)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-11770R-PE-Cy5.5
  • 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-11770R-PE-Cy5.5
    英文名称TMEM158 Rabbit pAb, PE-Cy5.5 conjugated
    中文名称PE-Cy5.5标记的跨膜蛋白158抗体
    英文别名40 kDa BINP binding protein; 40 kDa BINP-binding protein; BBP; BINP receptor; Brain injury derived neurotrophic peptide(BINP) binding protein; Brain specific binding protein; DKFZp586E1621; HBBP; p40BBP; Ras induced senescence protein 1; Ras-induced senescence protein 1; RIS1; TM158_HUMAN; TMEM 158; TMEM158; Transmembrane protein 158.
    产品应用Flow-Cyt=1μg/Test, 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 TMEM158
    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

    Neuroscience > Neurology process > Neurodegenerative disease

    Neuroscience > Neurotransmitter > Neuropeptides > More Neuropeptides

    亚细胞定位Membrane.
    翻译后修饰N-glycosylated.
    相似性Belongs to the TMEM158 family.
    功能Receptor for brain injury-derived neurotrophic peptide (BINP), a synthetic 13-mer peptide.
    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TMEM158 is a 286 amino acid protein encoded by a gene mapping to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

     

    应用推荐稀释比例
    {Flow-Cyt}{1μg/Test}
    {IF}{1:100-500}

     

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