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Mouse Glucose-dependent insulin-releasing polypeptide,GIP ELISA Kit

  • 中文名稱:
    小鼠葡萄糖依賴性胰島素釋放多肽(GIP)酶聯免疫試劑盒
  • 貨號:
    CSB-E08486m
  • 規格:
    96T/48T
  • 價格:
    ¥3200/¥2500
  • 其他:

產品詳情

  • 產品描述:
    小鼠葡萄糖依賴性胰島素釋放多肽(GIP)酶聯免疫試劑盒(CSB-E08486m)為雙抗夾心法ELISA試劑盒,定量檢測血清、血漿、組織勻漿樣本中的GIP含量。GIP(葡萄糖依賴性促胰島素釋放多肽)是一種腸促胰島素激素,參與糖代謝和脂代謝,通過多種途徑增加胰島素敏感性,改善胰島素抵抗。其研究機制涉及調節脂肪細胞代謝、促進β細胞增殖等,對治療2型糖尿病和肥胖具有重要意義。試劑盒檢測范圍為0.156 ng/mL-10 ng/mL,適用于科研領域探索GIP在糖代謝調控、胰島素分泌及能量平衡中的作用機制。該產品適用于小鼠模型中GIP與糖尿病、肥胖癥或胃腸道功能相關的基礎研究,實驗結果需結合其他代謝指標進行綜合分析,嚴禁用于臨床診斷。本品僅用于科研,不用于臨床診斷,產品具體參數及操作步驟詳見產品說明書。
  • 別名:
    GipGastric inhibitory polypeptide ELISA Kit; GIP ELISA Kit; Glucose-dependent insulinotropic polypeptide ELISA Kit
  • 縮寫:
  • Uniprot No.:
  • 種屬:
    Mus musculus (Mouse)
  • 樣本類型:
    serum, plasma, tissue homogenates
  • 檢測范圍:
    0.156 ng/mL-10 ng/mL
  • 靈敏度:
    0.039 ng/mL
  • 反應時間:
    1-5h
  • 樣本體積:
    50-100ul
  • 檢測波長:
    450 nm
  • 研究領域:
    Signal Transduction
  • 測定原理:
    quantitative
  • 測定方法:
    Sandwich
  • 精密度:
    Intra-assay Precision (Precision within an assay): CV%<8%        
    Three samples of known concentration were tested twenty times on one plate to assess.    
    Inter-assay Precision (Precision between assays): CV%<10%        
    Three samples of known concentration were tested in twenty assays to assess.      
                   
  • 線性度:
    To assess the linearity of the assay, samples were spiked with high concentrations of mouse GIP in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.  
      Sample Serum(n=4)    
    1:1 Average % 88    
    Range % 84-92    
    1:2 Average % 97    
    Range % 94-101    
    1:4 Average % 102    
    Range % 97-108    
    1:8 Average % 94    
    Range % 89-98    
  • 回收率:
    The recovery of mouse GIP spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.  
     
    Sample Type Average % Recovery Range    
    Serum (n=5) 102 98-107    
    EDTA plasma (n=4) 93 82-97    
                   
                   
  • 標準曲線:
    These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.  
     
    ng/ml OD1 OD2 Average Corrected    
    10 2.134 2.257 2.196 2.080    
    5 1.675 1.739 1.707 1.591    
    2.5 1.144 1.185 1.165 1.049    
    1.25 0.672 0.696 0.684 0.568    
    0.625 0.404 0.423 0.414 0.298    
    0.312 0.288 0.293 0.291 0.175    
    0.156 0.202 0.209 0.206 0.090    
    0 0.115 0.117 0.116      
  • 數據處理:
  • 貨期:
    3-5 working days

產品評價

靶點詳情

  • 功能:
    Potent stimulator of insulin secretion and relatively poor inhibitor of gastric acid secretion.
  • 基因功能參考文獻:
    1. GIP stimulation induces a switch in GIPR recycling from a rapid endosomal to a slow trans-Golgi network (TGN) pathway. GPCR kinases and b-arrestin2 are required for this switch in recycling. PMID: 27974210
    2. GIP provides a novel link between the immune system and the gut, with proinflammatory-immune modulatory function but minor glucose regulatory relevance in the context of acute endotoxemia. PMID: 27350651
    3. our data suggest that the metabolic hormone GIP plays an important role in bone marrow hematopoiesis PMID: 28250160
    4. It was demonstrated that cardiomyocytes represent a direct target of GIP action in vitro, and that GIP ameliorated AngII-induced cardiac hypertrophy via suppression of cardiomyocyte enlargement, apoptosis, and fibrosis in vivo. PMID: 27375170
    5. The loss of food-induced GIP response in Roux-limb of intestine likely contributes to the attenuated serum GIP response to feeding. PMID: 26266950
    6. GIP induces the expression of the proatherogenic cytokine osteopontin (OPN) in mouse arteries via local release of endothelin-1 and activation of CREB. GIPR mRNA is higher in symptomatic carotid endarterectomy patients. PMID: 26395740
    7. These studies support the hypothesis that a reduction in GIP signaling using a GIP-neutralizing mAb might provide a useful method for the treatment and prevention of obesity and related disorders. PMID: 26487006
    8. This study provides evidences that GIP acts directly on osteoblasts and is capable of improving collagen maturity and fibril diameter. PMID: 25582623
    9. There was decrease in GIP gene transcripts and protein in the gut of HNF1a-null mice. PMID: 25979074
    10. Circulating levels of GIP were significantly decreased in FABP5-deficient mice. PMID: 25268051
    11. phosphatidylinositol 3-kinase gamma has a role in insulin secretion induced by glucose-dependent insulinotropic polypeptide PMID: 25288806
    12. The results describe key beneficial immunoregulatory properties for glucose-dependent insulinotropic polypeptide in diet-induced obesity and reveal that its augmentation ameliorates adipose tissue inflammation and improves insulin resistance. PMID: 25217161
    13. GIP-reduced mice demonstrate that partial reduction of GIP does not extensively alter glucose tolerance, but it alleviates obesity and lessens the degree of insulin resistance under high-fat diet conditions, suggesting a potential therapeutic value. PMID: 24584548
    14. It was concluded from these observations that GIP, but not glucagon-like peptide-1, directly activates PepT1 activity by a cAMP-dependent signaling pathway in jejunum. PMID: 24072682
    15. A novel acylated form of (d-Ala(2))GIP with improved antidiabetic potential, lacking effect on body fat stores. PMID: 23518200
    16. The results indicated that ectopic glucose-dependent insulinotropic polypeptide expression in pancreatic beta cells maintains insulin secretion in the absence of proglucagon-derived peptides, revealing a novel mechanism for sustaining incretin action. PMID: 23099862
    17. Rfx6 increases GIP expression and content in enteroendocrine K-cells and is involved in GIP hypersecretion in high fat diet-induced obesity. PMID: 23192339
    18. GIP signaling may play a role in early embryonic pancreas differentiation to form insulin-positive cells or beta-cells. PMID: 21270265
    19. truncated forms of GIP exhibit potent anti-diabetic actions, without pro-obesity effects, and that the C-terminus contributes to the lipogenic actions of GIP PMID: 20231880
    20. GIP is expressed in and secreted from pancreatic islets and promotes islet glucose competence and also could support islet development and/or survival. PMID: 20138041
    21. substantial quantities of glycated GIP exist within the intestines of diabetic ob/ob mice, suggesting that this may be a contributing factor to the physiological disarray of this syndrome PMID: 11954659
    22. a novel pathway of obesity promotion via GIP; GIP directly links overnutrition to obesity PMID: 12068290
    23. Novel insulin/GIP co-producing cell lines provide unexpected insights into Gut K-cell function in vivo. PMID: 12124779
    24. Calcium mobilization from intracellular and extracellular sources, independent from K(ATP) channels, regulates secretion from some, but not all, subpopulations of enteroendocrine cells. PMID: 12676650
    25. GIP is the major insulinotropic factor in the secretion of insulin in response to glucose load in K(ATP) channel-deficient mice. PMID: 15362972
    26. Transcription factor PDX-1 plays a critical role in the cell-specific expression of the GIP gene. PMID: 15486225
    27. The physiological importance of glucose-dependent insulinotropic polypeptide has been investigated in single and double incretin receptor knockout mice. PMID: 15780432
    28. PI3K/PKB/Foxo1 signaling mediates GIP suppression of bax gene expression, which is a key pathway by which GIP regulates beta-cell apoptosis in vivo PMID: 15817464
    29. GIP plays a crucial role in switching from fat oxidation to fat accumulation under the diminished insulin action as a potential target for secondary prevention of insulin resistance PMID: 16105663
    30. Because GIPR(-/-) mice exhibited an increased plasma calcium concentration after meal ingestion, GIP directly links calcium contained in meal to calcium deposition on bone. PMID: 16469773
    31. Prohormone convertase 1/3 is essential for processing of the glucose-dependent insulinotropic polypeptide precursor PMID: 16476726
    32. protein kinase B, LKB1, and AMP-activated protein kinase have roles in activation of lipoprotein lipase by glucose-dependent insulinotropic polypeptide in adipocytes PMID: 17244606
    33. Glucose-dependent insulinotropic peptide inhibits bone resorption and stimulates bone formation PMID: 17321229
    34. First characterization of the anatomical distribution of GIP-immunoreactive cells in the rat brain providing an anatomical framework for future investigations regarding the functions of GIP in the central nervous system. PMID: 17510976
    35. Administration of resistin to adipocytes mimicked the effects of GIP on the PKB/LKB1/AMPK/LPL pathway: increasing phosphorylation of PKB, reducing levels of phosphorylated LKB1 and AMPK, and increasing LPL activity. PMID: 17890220
    36. genetic inactivation of GIP signaling can prevent the development of aging-associated insulin resistance through body composition changes PMID: 17937928
    37. GATA-4 may function to augment or enhance GIP expression rather than act as an initiator of GIP transcription. PMID: 18343025
    38. Gpr40 modulates FFA-stimulated insulin secretion from beta-cells not only directly but also indirectly via regulation of incretin(GIP and GLP-1) secretion PMID: 18519800
    39. The GIP-induced increase in glucose transport appears to be mediated, at least in part, by SGLT-1. PMID: 18719661
    40. These results indicate that inhibition of GIP signaling increases adiponectin levels, resulting in increased fat oxidation in peripheral tissues under high-fat diet. PMID: 18723001

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  • 亞細胞定位:
    Secreted.
  • 蛋白家族:
    Glucagon family
  • 數據庫鏈接:


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