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      abs997 (1 Citations)

      Ready to use immunohistochemical secondary antibody kit (anti mouse)

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      packaging: 5ml (can be used for 50 pieces)

      applicable: primary antibody is from mouse

      chromogenic substrate: dab (benzidine)

      reagent composition:

      component name specification quantity
      Endogenous peroxidase blocker 5ml1
      HRP enzyme labeled anti mouse secondary antibody polymer 5ml1
      DAB substrate (20×)0.25ml1
      DAB diluent 5ml1
      Hematoxylin 5ml1

       reagents not provided but required: primary antibody (from mouse), 5% goat serum (abs933), pbst

      this kit is the latest generation of non biotin detection system for immunohistochemical secondary antibody based on polymer technology, with stronger signal and simpler operation. Compared with the traditional immunohistochemical secondary antibody kit, it has three characteristics: first, due to the uniqueness of the polymer, the polymer molecule formed by the direct combination of enzyme molecules and secondary antibody IgG molecules is highly sensitive, effectively reducing the amount of primary antibody used, and the primary antibody reagent can be diluted 2-4 times; Second, because the use of biotin is avoided, the non-specific background color development caused by biotin can be avoided, and a clearer color development and cleaner background can be obtained; Third, rapid and shorter reagent incubation time

      storage and validity period

      2-8° C save. Each component can be stored for at least 12 months



      operation steps:

      note: all the steps are operated at room temperature. The reagent can be directly titrated in a drop bottle or with a pipette. One drop =30-40ul

      1Dewaxed and hydrated tissue sections

      2Wash 2-3 times in PBST for 5 minutes

      3According to the special requirements of the applied primary antibody, the tissue sections were pretreated (antigen retrieval)

      4Wash 2-3 times in PBST for 5 minutes

      5Add 100ul endogenous peroxidase blocking agent was incubated for 10 min to block endogenous peroxidase to reduce nonspecific background staining

      6Wash 2-3 times in PBST for 5 minutes

      7Add 100ul of 5% to 10% normal goat serum and incubate for 20 minutes at room temperature. If the primary antibody is diluted in a buffer containing 5% to 10% normal goat serum, this step can be omitted

      8Wash 2-3 times in PBST for 5 minutes

      9Add primary antibody and incubate at room temperature or 37 ℃ for 30 min

      10Wash 2-3 times in PBST for 5 minutes

      11Add 100ul HRP enzyme labeled anti mouse & Rabbit secondary antibody polymer was incubated for 30 min   Note: this liquid is sensitive to light, and keep away from light

      12Wash 2-3 times in PBST for 5 minutes

      13Use freshly prepared dab chromogenic solution (Dilute with dab Dilution DAB substrate , ready to use) , incubate at room temperature for 5 minutes (the time can be adjusted according to the color development), and rinse the slide with tap water

      14Add 100ulhematoxylin , incubate for 3 minutes (the time can be appropriately adjusted according to the color development), and rinse with tap water to return to blue

      15Dehydrated, transparent, sealed

      Tips : This product is for research use only. Not for use in diagnostic prodcedures.
      Dear customer, if you have any questions or want to know about our products, you can click the "I want to ask" button to fill in your questions. Unsuccessful submission? Please contact worldwide@absin.cn.
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      Effects and translatomics characteristics of a small-molecule inhibitor of METTL3 against non-small cell lung cancer

      Han Xiao, Rong Zhao, Wangyang Meng, Yongde Liao

      Journal of Pharmaceutical Analysis. 2023 Apr 19 .

      Influencing factors:14.026

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