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Mouse Angiopoietin-related protein 3(ANGPTL3) ELISA kit

  • 中文名稱(chēng):
    小鼠血管生成素相關(guān)蛋白3(ANGPTL3)酶聯(lián)免疫試劑盒
  • 貨號(hào):
    CSB-EL001711MO
  • 規(guī)格:
    96T/48T
  • 價(jià)格:
    ¥3600/¥2500
  • 其他:

產(chǎn)品詳情

  • 產(chǎn)品描述:
    小鼠血管生成素相關(guān)蛋白3(ANGPTL3)酶聯(lián)免疫試劑盒(CSB-EL001711MO)為雙抗夾心法ELISA試劑盒,定量檢測(cè)血清、血漿、組織勻漿樣本中的ANGPTL3含量。ANGPTL3是一種由肝臟分泌的糖蛋白,參與脂蛋白代謝調(diào)節(jié),抑制LPL活性,影響VLDL、TG、LDL-C和HDL-C水平。其功能缺失突變可導(dǎo)致家族性混合型低脂血癥,而抑制ANGPTL3可能降低ASCVD風(fēng)險(xiǎn)。目前,ANGPTL3已成為治療血脂異常的潛在靶點(diǎn),相關(guān)siRNA藥物正在研發(fā)中。試劑盒檢測(cè)范圍為31.25 pg/mL-2000 pg/mL,靈敏度為10.24 pg/mL。適用于小鼠疾病模型中ANGPTL3表達(dá)動(dòng)態(tài)分析、代謝機(jī)制研究或藥物干預(yù)效果評(píng)估等科研用途。本品僅用于科研,不用于臨床診斷,產(chǎn)品具體參數(shù)及操作步驟詳見(jiàn)產(chǎn)品說(shuō)明書(shū)。
  • 別名:
    Angptl3Angiopoietin-related protein 3 ELISA kit; Angiopoietin-like protein 3) [Cleaved into: ANGPTL3(17-224)] ELISA kit
  • 縮寫(xiě):
  • Uniprot No.:
  • 種屬:
    Mus musculus (Mouse)
  • 樣本類(lèi)型:
    serum, plasma, tissue homogenates
  • 檢測(cè)范圍:
    31.25 pg/mL-2000 pg/mL
  • 靈敏度:
    10.24 pg/mL
  • 反應(yīng)時(shí)間:
    1-5h
  • 樣本體積:
    50-100ul
  • 檢測(cè)波長(zhǎng):
    450 nm
  • 研究領(lǐng)域:
    Cardiovascular
  • 測(cè)定原理:
    quantitative
  • 測(cè)定方法:
    Sandwich
  • 數(shù)據(jù)處理:
  • 貨期:
    3-5 working days

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

  • 最新研究進(jìn)展:
        ANGPTL3(angiopoietin-like protein 3)是一種由肝臟和腸道分泌的蛋白質(zhì),能夠調(diào)節(jié)脂質(zhì)代謝和胰島素敏感性。近年來(lái),關(guān)于ANGPTL3的研究得到了越來(lái)越多的關(guān)注。
        最新的研究表明,ANGPTL3是一種抑制性蛋白,可以通過(guò)抑制肝臟和腸道的脂質(zhì)合成來(lái)調(diào)節(jié)血脂水平。一些研究還發(fā)現(xiàn),ANGPTL3缺陷會(huì)導(dǎo)致高密度脂蛋白膽固醇(HDL-C)水平的升高和低密度脂蛋白膽固醇(LDL-C)水平的降低,因此被認(rèn)為是一種可靶向的治療靶點(diǎn)。
        針對(duì)ANGPTL3的藥物治療也得到了廣泛的研究。目前已經(jīng)開(kāi)發(fā)出多種針對(duì)ANGPTL3的藥物,包括單抗和小分子抑制劑等。這些藥物的研究結(jié)果表明,針對(duì)ANGPTL3的治療能夠顯著降低血脂水平,并有望成為一種有效的治療高脂血癥的方法。
  • 功能:
    Acts in part as a hepatokine that is involved in regulation of lipid and glucose metabolism. Proposed to play a role in the trafficking of energy substrates to either storage or oxidative tissues in response to food intake. Has a stimulatory effect on plasma triglycerides (TG), which is achieved by suppressing plasma TG clearance via inhibition of LPL activity; the function seems to be specific for the feeding conditions. The inhibition of LPL activity appears to be an indirect mechanism involving recruitment of proprotein convertases PCSK6 and FURIN to LPL leading to cleavage and dissociation of LPL from the cell surface; the function does not require ANGPTL3 proteolytic cleavage but seems to be mediated by the N-terminal domain, and is not inhibited by GPIHBP1. Can inhibit endothelial lipase, causing increased plasma levels of high density lipoprotein (HDL) cholesterol and phospholipids; the cleaved N-terminal domain is more efficient than the uncleaved proprotein. Can bind to adipocytes to activate lipolysis, releasing free fatty acids and glycerol. Suppresses LPL specifically in oxidative tissues which is required to route very low density lipoprotein (VLDL)-TG to white adipose tissue (WAT) for storage in response to food; the function may involve cooperation with circulating, liver-derived ANGPTL8 and ANGPTL4 expression in WAT. Contributes to lower plasma levels of low density lipoprotein (LDL)-cholesterol by a mechanism that is independent of the canonical pathway implicating APOE and LDLR. May stimulate hypothalamic LPL activity.; Involved in angiogenesis. Binds to endothelial cells via integrin alpha-V/beta-3 (ITGAV:ITGB3), activates FAK, MAPK and Akt signaling pathways and induces cell adhesion and cell migration. May increase the motility of podocytes. Secreted from podocytes, may modulate properties of glomerular endothelial cells involving integrin alpha-V/beta-3 and Akt signaling. May induce actin filament rearrangements in podocytes implicating integrin alpha-V/beta-3 and Rac1 activation. Binds to hematopoietic stem cells (HSC) and is involved in the regulation of HSC activity probably implicating down-regulation of IKZF1/IKAROS.
  • 基因功能參考文獻(xiàn):
    1. The role of ANGPLT3 in controlling lipoprotein metabolism and risk of cardiovascular diseases is reviewed here. PMID: 29334984
    2. ANGPTL8 has a functional LPL inhibitory motif, but only inhibits LPL and increases plasma TG levels in mice in the presence of ANGPTL3 PMID: 28413163
    3. The data suggests that ANGPTL3 is part of the machinery causing dyslipidemia majorily via LPL inhibition in mastitis mice. PMID: 29104012
    4. Using in vitro ketosis model by glucose starvation, studied inhibition of ketosis by momilactone B. Found momilactone B could regulate the angiopoietin-like-3 (ANGPTL3)-lipoprotein lipase (LPL)pathway, and suppressed the expression of HMGCS2 through the increased expression of STAT5b. PMID: 27874312
    5. This model suggests a general mechanism by which TAG trafficking is coordinated by lipasin, Angptl3 and Angptl4 at different nutritional statuses. PMID: 26687026
    6. Inactivation of ANGPTL3 reduces hepatic VLDL-triglyceride secretion PMID: 25954050
    7. The deletion of ANGPTL3 tremendously attenuates proteinuria and protects podocytes from injury in a mouse model of adriamycin-induced nephropathy. PMID: 25710887
    8. ANGPTL3 has a role in regulating white adipose tissue energy homeostasis but not in liver PMID: 26305978
    9. Data indicate that expression of Angptl3 in hematopoietic stem cell (HSC) through lentiviral transduction promoted HSC expansion. PMID: 25170927
    10. Angptl3 could induce actin filament rearrangement, mainly in lamellipodia formation, and that this process was mediated by integrin alpha(V)beta-mediated FAK and PI3K phosphorylation and Rac1 activation. PMID: 24294595
    11. Furin has a role as the primary in vivo convertase of ANGPTL3 and endothelial lipase in hepatocytes PMID: 23918928
    12. ANGPTL8, a paralog of ANGPTL3 that arose through duplication of an ancestral DOCK gene, regulates postprandial TAG and fatty acid metabolism by controlling activation of its progenitor, and perhaps other ANGPTLs PMID: 23150577
    13. Angptl3, as an extrinsic factor, thus supports the stemness of hematopoietic stem cells in the bone marrow niche. PMID: 20959605
    14. ANGPTL3 expression is upregulated in puromycin-induced podocyte damage and is associated with the reduction of perlecan and agrin expression PMID: 20424482
    15. a molecular connection between ANGPTL3, lipoprotein lipase, and proprotein convertases PMID: 20581395
    16. ANGPTL3 to be capable of regulating the motility and permeability of podocytes and that the mechanism of ANGPTL3's regulation could be associated with the altered expression of nephrin. PMID: 20633534
    17. Like ANGPTL4, ANGPTL3 inhibited nonstabilized LPL but not GPIHBP1-stabilized LPL PMID: 19542565
    18. ANGPTL3 stimulates endothelial cell adhesion and migration via integrin alpha vbeta 3 and induces blood vessel formation in vivo PMID: 11877390
    19. affects VLDL triglyceride clearance by interfering with LPL activity PMID: 12097324
    20. hepatic Angptl3 has a role in hypertriglyceridemia associated with the treatment of LXR ligand PMID: 12672813
    21. the cleavage of ANGPTL3 at two sites is important for the activation of ANGPTL3 in vivo PMID: 12909640
    22. Expression of ANGPTL3 was enhanced in both insulin-deficient and -resistant diabetic states; results strongly suggest ANGPTL3 to play an important role in hyperlipidemia in diabetes. PMID: 15094378
    23. Elevated ANGPTL3 by leptin- or insulin-resistance is attributed to increased plasma triglycerides and free fatty acid levels in obesity. PMID: 15336575
    24. Differential regulation of Angptl3 and Angptl4 by sites of expression, nutritional status, and ligands of nuclear receptors may confer unique roles of each in lipoprotein metabolism. Angptl3 is a target gene of liver X receptor PMID: 15863837
    25. Angptl3-deficiecy displayed hypotriglyceridemia with elevated postheparin plasma lipoprotein lipase, with greater effect in fed state. Deficiecy in both Angptl proteins had additive effect on plasma triglycerides with survival not past 2 months of age. PMID: 16081640
    26. Angptl3 acts as an inhibitor of EL and may be involved in the regulation of plasma HDL cholesterol and HDL-PL levels in humans and rodents. PMID: 17110602
    27. SE1 region of ANGPTL3 and ANGPTL4 functions as a domain important for binding LPL and inhibiting its activity in vitro and in vivo. PMID: 19318355

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  • 亞細(xì)胞定位:
    Secreted. Cell projection, lamellipodium.
  • 組織特異性:
    Predominantly expressed in liver, weakly expressed in kidney and lung. Expressed in podocytes (at protein level). Expressed in hypothalamic neurons (at protein level). Expressed in bone marrow sinusoidal endothelial cells (at protein level).
  • 數(shù)據(jù)庫(kù)鏈接:


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