PLCD1/NDNC3 Rabbit pAb, HRP conjugated(bs-12714R-HRP)-100ul

PLCD1/NDNC3 Rabbit pAb, HRP co

njugated(bs-12714R-HRP)-100ul
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  • ¥2980
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  • bs-12714R-HRP
  • 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-12714R-HRP
    英文名称PLCD1/NDNC3 Rabbit pAb, HRP conjugated
    中文名称HRP标记的磷酸肌醇磷脂酶C抗体
    英文别名1-phosphatidylinositol 4, 5-bisphosphate phosphodiesterase delta 1; NDNC3; phosphoinositide phospholipase C; phosphoinositide phospholipase C delta 1; phospholipase C delta 1; phospholipase C III; PLC delta 1; PLC III.PLCD1_HUMAN
    产品应用IHC-P=1:100-500, IHC-F=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 PLCD1/NDNC3
    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 > Second Messenger > Lipid Messengers

    相似性Contains 1 C2 domain.
    _x000D_ Contains 2 EF-hand domains.
    _x000D_ Contains 1 PH domain.
    _x000D_ Contains 1 PI-PLC X-box domain.
    _x000D_ Contains 1 PI-PLC X-box domain.
    功能The production of the second messenger molecules diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3) is mediated by activated phosphatidylinositol-specific phospholipase C enzymes. Essential for trophoblast and placental development.
    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This gene encodes a member of the phospholipase C family. Phospholipase C isozymes play critical roles in intracellular signal transduction by catalyzing the hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) into the second messengers diacylglycerol (DAG) and inositol triphosphate (IP3). The encoded protein functions as a tumor suppressor in several types of cancer, and mutations in this gene are a cause of hereditary leukonychia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

     

    应用推荐稀释比例
    {IHC-P}{1:100-500}
    {IHC-F}{1:100-500}

     

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