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ATP-dependent RNA helicase DDX

39A, Ddx39a ELISA KIT/ Mouse ATP-dependent RNA helicase DDX39A, Ddx39a ELISA试剂盒
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  • ¥2980
  • LSM Bio
  • 78-5000pg/ml
  • 39pg/ml
  • 进口
  • ELI-32917m
  • 2025年07月13日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      50

    • 供应商

      LSM BIO

    • 检测范围

      78-5000pg/ml

    • 检测方法

      夹心法ELISA

    • 应用

      检测小鼠血清,血浆,组织匀浆内的目标蛋白含量

    • 适应物种

      小鼠

    • 标记物

      ATP-dependent RNA helicase DDX39A, Ddx39a

    • 样本

      小鼠血清,血浆,组织匀浆

    • 灵敏度

      39pg/ml

    • 规格

      96Tests

    Mouse ATP- dependent RNA helicase DDX39A, Ddx39a ELISA KIT

    Product Name:Mouse ATP- dependent RNA helicase DDX39A, Ddx39a ELISA KIT
    Packing:96T

    Catalog No.:ELI-32917m

    Gene Name:Mouse Ddx39a

    Detect Range:0.156-10ng/ml

    Sensitivity:0.094ng/ml

    Target Protein Name:Mouse Ddx39a

    Alternative Name:Mouse ATP-dependent RNA helicase DDX39A, Ddx39a
    Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

    ELISA type:Sandwich ELISA Kit
    Product Description:Mouse ATP- dependent RNA helicase DDX39A, Ddx39a ELISA KIT allows for the in vitro quantitative determination of Mouse Ddx39a concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

    ELISA Test Principle:
    The microtiter plate provided in Mouse ATP- dependent RNA helicase DDX39A, Ddx39a ELISA KIT has been pre-coated with an Mouse ATP-dependent RNA helicase DDX39A, Ddx39a antibody specific to Mouse Ddx39a .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Ddx39a and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Mouse Ddx39a , biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm.The concentration of Mouse Ddx39a in the samples is then determined by comparing the O.D. of the samples to the standard curve.

    NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!

     

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    图标文献和实验
    该产品被引用文献
    Article: Quercetin and lithium chloride potentiate the protective effects of carvedilol against renal ischemia-reperfusion injury in high-fructose, high-fat diet-fed swiss albino mice independent of renal lipid signaling Author:Asmaa M.RezkabIslam A.A.E.-H.IbrahimaMona F.MahmoudaAmr A.A.Mahmouda1 Received 6 September 2020, Revised 12 October 2020, Accepted 28 October 2020, Available online 4 November 2020. Chemico-Biological Interactions Available online 4 November 2020, 109307 doi: doi.org/10.1016/j.cbi.2020.109307
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    • Linear amplification of limiting amounts of RNA for gene expression studies

      Add 10µl mix to the RNA/primer sample and incubate at 42°C for 1 hour. Second strand synthesis (in RNAse-free PCR tubes) Prepare the following mix: 86µl DEPC-H2 O, 30µl 5x second strand buffer, 3µl 10mM dNTP mix, 8µl DNA Polymerase

    • RNA Analysis by Nuclease Protection

      Figure 5.1.2 Typical RNase protection assay using a probe for mouse β‐actin. A 300‐base mouse β‐actin probe was hybridized to two‐fold‐increasing amounts of mouse total‐liver RNA (from 0.625 to 10 µg; lanes 4 to 8) and analyzed by RNase protection

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    文献支持
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    ¥2980