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糖原合酶激酶-3β单克隆抗体

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  • ¥1200
  • Biorigin
  • 2025年11月27日
  • WB,IHC-P,
  • Human,Mouse,Rat,
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 适应物种

      Human,Mouse,Rat,

    • 应用范围

      WB,IHC-P,

    • 抗体英文名

      GSK-3 Beta

    • 规格

      50ul

    英文名称 GSK-3 Beta
    中文名称 糖原合酶激酶-3β单克隆抗体
    别    名 glycogen synthase kinase 3 beta; GSK 3 beta; GSK 3B; GSK3B; GSK3B protein; GSK3beta isoform; GSK3 beta; Glycogen synthase kinase-3 beta; GSK-3 beta; GSK3B_HUMAN. 

     

    研究领域 细胞生物  转录调节因子  激酶和磷酸酶  
    抗体来源 Mouse
    克隆类型 Monoclonal
    克 隆 号 3A6
    交叉反应 Human, Mouse, Rat, 
    产品应用 WB=1:500-1000 ELISA=1:1000-5000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:200-500 (石蜡切片需做抗原修复)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量 47kDa
    细胞定位 细胞核 细胞浆 细胞膜 
    性    状 Liquid
    浓    度 1mg/ml
    免 疫 原 KLH conjugated Synthesised phosphopeptide derived from human GSK-3 Beta around the phosphorylation site of Ser21+Ser29: 
    亚    型 IgG
    纯化方法 affinity purified by Protein G
    储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMed PubMed
    产品介绍 The protein encoded by this gene is a serine-threonine kinase, belonging to the glycogen synthase kinase subfamily. It is involved in energy metabolism, neuronal cell development, and body pattern formation. Polymorphisms in this gene have been implicated in modifying risk of Parkinson disease, and studies in mice show that overexpression of this gene may be relevant to the pathogenesis of Alzheimer disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]

    Function:
    Constitutively active protein kinase that acts as a negative regulator in the hormonal control of glucose homeostasis, Wnt signaling and regulation of transcription factors and microtubules, by phosphorylating and inactivating glycogen synthase (GYS1 or GYS2), EIF2B, CTNNB1/beta-catenin, APC, AXIN1, JUN, NFATC1/NFATC, MAPT/TAU and MACF1. Requires primed phosphorylation of the majority of its substrates. In skeletal muscle, contributes to insulin regulation of glycogen synthesis by phosphorylating and inhibiting GYS1 activity and hence glycogen synthesis. May also mediate the development of insulin resistance by regulating activation of transcription factors. Regulates protein synthesis by controlling the activity of initiation factor 2B (EIF2BE/EIF2B5) in the same manner as glycogen synthase. In Wnt signaling, GSK3B forms a multimeric complex with APC, AXIN1 and CTNNB1/beta-catenin and phosphorylates the N-terminus of CTNNB1 leading to its degradation mediated by ubiquitin/proteasomes. Phosphorylates JUN at sites proximal to its DNA-binding domain, thereby reducing its affinity for DNA. Phosphorylates NFATC1/NFATC on conserved serine residues promoting NFATC1/NFATC nuclear export, shutting off NFATC1/NFATC gene regulation, and thereby opposing the action of calcineurin. Phosphorylates MAPT/TAU on 'Thr-548', decreasing significantly MAPT/TAU ability to bind and stabilize microtubules. MAPT/TAU is the principal component of neurofibrillary tangles in Alzheimer disease. Plays an important role in ERBB2-dependent stabilization of microtubules at the cell cortex. Phosphorylates MACF1, inhibiting its binding to microtubules which is critical for its role in bulge stem cell migration and skin wound repair. Probably regulates NF-kappa-B (NFKB1) at the transcriptional level and is required for the NF-kappa-B-mediated anti-apoptotic response to TNF-alpha (TNF/TNFA). Negatively regulates replication in pancreatic beta-cells, resulting in apoptosis, loss of beta-cells and diabetes. Phosphorylates MUC1 in breast cancer cells, decreasing the interaction of MUC1 with CTNNB1/beta-catenin. Is necessary for the establishment of neuronal polarity and axon outgrowth. Phosphorylates MARK2, leading to inhibit its activity. Phosphorylates SIK1 at 'Thr-182', leading to sustain its activity.

    Subunit:
    Monomer. Interacts with ARRB2 and DISC1. Interacts with CABYR, MMP2, MUC1, NIN and PRUNE Interacts with AXIN1; the interaction mediates hyperphosphorylation of CTNNB1 leading to its ubiquitination and destruction. Interacts with and phosphorylates SNAI1. Interacts with DNM1L (via a C-terminal domain). Found in a complex composed of MACF1, APC, AXIN1, CTNNB1 and GSK3B.

    Subcellular Location:
    Cytoplasm. Nucleus. Cell membrane. Note=The phosphorylated form shows localization to cytoplasm and cell membrane. The MEMO1-RHOA-DIAPH1 signaling pathway controls localization of the phosophorylated form to the cell membrane.

    Tissue Specificity:
    Expressed in testis, thymus, prostate and ovary and weakly expressed in lung, brain and kidney.

    Post-translational modifications:
    Phosphorylated by AKT1 and ILK1. Upon insulin-mediated signaling, the activated PKB/AKT1 protein kinase phosphorylates and desactivates GSK3B, resulting in the dephosphorylation and activation of GYS1. Activated by phosphorylation at Tyr-216.

    Similarity:
    Belongs to the protein kinase superfamily. CMGC Ser/Thr protein kinase family. GSK-3 subfamily.
    Contains 1 protein kinase domain.

    SWISS:
    P49841

    Gene ID:
    2932

    Database links:

    Entrez Gene: 2932 Human

    Entrez Gene: 56637 Mouse

    Entrez Gene: 84027 Rat

    Omim: 605004 Human

    SwissProt: P49841 Human

    SwissProt: Q9WV60 Mouse

    SwissProt: P18266 Rat

    Unigene: 445733 Human

    Unigene: 394930 Mouse

    Unigene: 10426 Rat



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications

     

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    图标文献和实验
    相关实验
    • 【求助】关于gsk3-beta功能的疑问

      -3beta的活性问题, 例如说, 文献中说gsk在基础状态下士处于一种低活性状态,这个低活性状态的意思指的是第九位的含量高还是指216位的含量低? 另外,gsk3-beta在糖代谢途径中发挥作用的话是否需要216位的磷酸化才能磷酸化糖原合酶?或者说是不是没有216位也能磷酸化糖原合酶?只是有了216位后磷酸化作用更强? 问题可能有点浅显~~~ zhangyinghua8106 我最近也因为GSK-3 beta 总蛋白与磷酸化蛋白活性之间

    • Mol Cell:杨薇等揭示 DNA-PK 的激活机制以及自磷酸化对 NHEJ 通路的重要作用​

      70/80 的核心(⍺/β 结构域和 β 桶结构域)与 DNA-PKcs 的 N-HEAT 个 M-HEAT 结构域相互作用以外,Ku80-CTR 的螺旋 548-555、结构域 595-706 和螺旋 724-732 也分别固定了 DNA-PKcs 底座的四个角,对 DNA-PK 激活起到固定和促进作用。 DNA-PK 激活过程中的结构变化 A-D 分别为 N-HEAT、M-HEAT、FAT 和激酶结构域的构象变化,PQR 无序部分结构显示为虚线,底物 ATP 和多肽显示为棍棒模型,E 为 激活态

    • 糖代谢复习笔记

      是体内唯一降血糖的激素。 1,促进肌肉,脂肪细胞载体转运葡萄糖入内,2, 糖原磷酸化酶活性降低(通过对蛋白激酶A的抑制); 糖原合酶的活性升高(激活糖原合酶脱磷酸酶),加速肝,肌肉糖原的合成,3,通过第二信使间接激活丙酮酸脱氢酶(丙酮酸从胞液到乙酰CoA的反应,部位是线粒体),加速丙酮酸氧化脱羧成为乙酰CoA, 4, 抑制磷酸烯醇式丙酮酸羧激酶活性, 促进氨基酸进入肌肉合成蛋白质,从而降低糖异生。降低血糖。 5, 减少脂肪组织动员脂肪酸,促进糖有氧氧化。 B 胰高血糖素 胰腺α细胞分泌的。 升高

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