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    2. 最近搜索:細胞培養 微生物學 分子生物 生物化學
      首頁>>免疫學>>一抗>>D型-過氧化酶活化增生受體抗體
      D型-過氧化酶活化增生受體抗體
      • 產品貨號:
        BN41520R
      • 中文名稱:
        D型-過氧化酶活化增生受體抗體
      • 英文名稱:
        Rabbit anti-PPAR delta + beta Polyclonal antibody
      • 品牌:
        Biorigin
      • 貨號

        產品規格

        售價

        備注

      • BN41520R-50ul

        50ul

        ¥1486.00

        交叉反應:Human,Mouse(predicted:Rat) 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

      • BN41520R-100ul

        100ul

        ¥2360.00

        交叉反應:Human,Mouse(predicted:Rat) 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

      • BN41520R-200ul

        200ul

        ¥3490.00

        交叉反應:Human,Mouse(predicted:Rat) 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

      產品描述

      英文名稱PPAR delta + beta
      中文名稱D型-過氧化酶活化增生受體抗體
      別    名PPAR delta+beta; FAAR; MGC3931; NR1C2; NUC1; NUCI; NUCII; Nuclear hormone receptor 1; Nuclear receptor subfamily 1 group C member 2; Peroxisome proliferative activated receptor delta; Peroxisome proliferator-activated receptor beta (PPAR-beta); Peroxisome proliferator-activated receptor beta; Peroxisome proliferator-activated receptor delta; PPAR beta; PPAR-beta; PPAR-delta; PPAR-? PPARB; PPARD; PPARD_HUMAN.  
      研究領域心血管  免疫學  細胞膜受體  
      抗體來源Rabbit
      克隆類型Polyclonal
      交叉反應Human,  (predicted: Mouse, Rat, )
      產品應用ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1ug/Test IF=1:100-500 (石蠟切片需做抗原修復)
      not yet tested in other applications.
      optimal dilutions/concentrations should be determined by the end user.
      分 子 量48kDa
      細胞定位細胞核 
      性    狀Liquid
      濃    度1mg/ml
      免 疫 原KLH conjugated synthetic peptide derived from mouse PPAR-delta:2-100/440 
      亞    型IgG
      純化方法affinity purified by Protein A
      儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
      保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
      PubMedPubMed
      產品介紹Receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the receptor binds to a promoter element in the gene for acyl-CoA oxidase and activates its transcription. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Heterodimer with the retinoid X receptor. Subcellular located at nuclear Tissue specificity: Heart, adrenal and intestine. Belongs to the nuclear hormone receptor family. NR1 subfamily. It Contains 1 nuclear receptor DNA-binding domain.

      Function:
      Ligand-activated transcription factor. Receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Has a preference for poly-unsaturated fatty acids, such as gamma-linoleic acid and eicosapentanoic acid. Once activated by a ligand, the receptor binds to promoter elements of target genes. Regulates the peroxisomal beta-oxidation pathway of fatty acids. Functions as transcription activator for the acyl-CoA oxidase gene. Decreases expression of NPC1L1 once activated by a ligand.

      Subcellular Location:
      Nucleus.

      Tissue Specificity:
      Ubiquitous with maximal levels in placenta and skeletal muscle.

      Similarity:
      Belongs to the nuclear hormone receptor family. NR1 subfamily.
      Contains 1 nuclear receptor DNA-binding domain.

      SWISS:
      P35396

      Gene ID:
      5467

      Database links:

      Entrez Gene: 5467 Human

      Entrez Gene: 19015 Mouse

      Entrez Gene: 25682 Rat

      Omim: 600409 Human

      SwissProt: Q03181 Human

      SwissProt: P35396 Mouse

      Unigene: 696032 Human

      Unigene: 328914 Mouse

      Unigene: 96181 Rat



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

      類固醇受體(Steroid Receptors)
      研究人員指出該分子的功能,極可能就是阻斷心血管免疫發炎反應的訊號傳遞過程。PPAR-delta基因是控制肌肉發展的重要基因,在增加老鼠耐力的同時還能幫助它燃燒掉脂肪,研究人員發現,對于與新陳代謝有關的各項疾病,從心臟病到肥胖癥都有啟發性的意義,他可以阻止脂肪沉淀在動脈壁上,進而防止動脈硬化癥的發生,該蛋白參與脂肪代謝、肥胖、糖尿病、動脈硬化和癌癥的發病。
      在動脈硬化現象發生的早期,免疫細胞會促使血管慢性的發炎,因而造成血管不斷地吸收和輸送脂肪,進而導致脂肪的堆積與血管硬化,而PPAR-delta就像警衛分子一樣,時時降低發炎反應和抑制動脈硬化斑的形成,因此該分子應該是相關藥物研發,相當值得切入的目標。
      研究人員認為,這個發現將給藥廠研發治療心血管疾病的新藥提供新的線索。




















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