Polycystin 1 Rabbit pAb, PE conjugated(bs-2157R-PE)-100ul

Polycystin 1 Rabbit pAb, PE co

njugated(bs-2157R-PE)-100ul
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  • ¥2980
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  • bs-2157R-PE
  • 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-2157R-PE
    英文名称Polycystin 1 Rabbit pAb, PE conjugated
    中文名称PE标记的多囊肾蛋白1抗体
    英文别名Autosomal dominant polycystic kidney disease protein 1; PBP; PKD; PKD1; Polycystic Kidney Disease 1; Polycystin 1 Precursor; PKD1; Pc-1; TRPP1; PKD1_HUMAN.
    产品应用Flow-Cyt=1μg/Test

    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 Polycystin 1
    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

    Cancer > Cancer Metabolism > Metabolic signaling pathway > Metabolism of lipids and lipoproteins

    Metabolism > Pathways and Processes > Metabolic signaling pathways > Lipid and lipoprotein metabolism > Lipid metabolism

    Metabolism > Types of disease > Cancer

    Signal Transduction > Growth Factors/Hormones > EGF

    Signal Transduction > Metabolism > Plasma Membrane > Channels

    Signal Transduction > Signaling Pathway > Calcium Signaling

    Signal Transduction > Signaling Pathway > Calcium Signaling > Calcium Channels

    亚基Interacts with PKD2. Interacts with PRKX; involved in differentiation and controlled morphogenesis of the kidney. Interacts with NPHP1 (via SH3 domain).
    亚细胞定位Membrane; Multi-pass membrane protein. Cell projection, cilium. Note=PKD1 localization to the plasma and ciliary membranes requires PKD2, is independent of PKD2 channel activity, and involves stimulation of PKD1 autoproteolytic cleavage at the GPS domain.
    翻译后修饰After synthesis, undergoes cleavage between Leu-3048 and Thr-3049 in the GPS domain. Cleavage at the GPS domain occurs through a cis-autoproteolytic mechanism involving an ester-intermediate via N-O acyl rearrangement. This process takes place in the early secretory pathway, depends on initial N-glycosylation, and requires the REJ domain. There is evidence that cleavage at GPS domain is incomplete. Uncleaved and cleaved products may have different functions in vivo.
    相似性Contains 1 C-type lectin domain._x000D_
    Contains 1 GPS domain._x000D_
    Contains 1 LDL-receptor class A domain._x000D_
    Contains 2 LRR (leucine-rich) repeats._x000D_
    Contains 1 LRRCT domain._x000D_
    Contains 1 LRRNT domain._x000D_
    Contains 17 PKD domains._x000D_
    Contains 1 PLAT domain._x000D_
    Contains 1 REJ domain._x000D_
    Contains 1 WSC domain.
    功能Involved in renal tubulogenesis. Involved in fluid-flow mechanosensation by the primary cilium in renal epithelium. Acts as a regulator of cilium length, together with PKD2. The dynamic control of cilium length is essential in the regulation of mechanotransductive signaling. The cilium length response creates a negative feedback loop whereby fluid shear-mediated deflection of the primary cilium, which decreases intracellular cAMP, leads to cilium shortening and thus decreases flow-induced signaling. May be an ion-channel regulator. Involved in adhesive protein-protein and protein-carbohydrate interactions.
    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 polycystin protein family. The encoded glycoprotein contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail. It is an integral membrane protein that functions as a regulator of calcium permeable cation channels and intracellular calcium homoeostasis. It is also involved in cell-cell/matrix interactions and may modulate G-protein-coupled signal-transduction pathways. It plays a role in renal tubular development, and mutations in this gene cause autosomal dominant polycystic kidney disease type 1 (ADPKD1). ADPKD1 is characterized by the growth of fluid-filled cysts that replace normal renal tissue and result in end-stage renal failure. Splice variants encoding different isoforms have been noted for this gene. Also, six pseudogenes, closely linked in a known duplicated region on chromosome 16p, have been described. [provided by RefSeq].

     

    应用推荐稀释比例
    {Flow-Cyt}{1μg/Test}

     

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