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FadeStop™ Fluorescent Mounting Medium with DAPI

#272

一键复制产品信息
Hela cells were stained with anti-CTCF antibody and mounted in FadeStop™ fuorescent mounting medium. lmages were taken 1 day (D1), 2 months (M2), and 4 months(M4) after staining using Zeiss LSM 880 confocal laser scanning microscope. Nuclei werestained blue with DAPl. ACTB was stained magenta with Alexa Fluor® 647. Scale bars, 20 um.
Hela cells were stained with CTCF antibody and mounted in FadeStop™ fluorescent mounting medium. The slide was stored at -20°C for 1 month before imaging using a ZeissLSM 880 confocal laser scanning microscope. A series of scans were performed to assess thephotobleaching speed of the fluorescent dye. Note that even after 12th can, the image quality was still high. Scale bars, 20 μm.
Please select the specifications of the product.
Specification:
Unit price:
$99.00
Quantity:
1
(Excluding sales tax)
  • Gene Symbol:
    -
  • Catalog:
    272
  • Application:
    ICC
  • Species Reactivity:
    -
Information

Description

FadeStop™ fluorescent mounting medium is specially formulated to prolong the intensity of the fluorescence used in immunocytochemical and immunohistochemical staining. Our products can keep the fluorescent dyes from photobleaching for at least four months if the slides are stored at -20°C.

Concentration of DAPI: 1.5 μg/mL

Application: Immunocytochemistry (IC)

Storage

Store bottles upright at 4°C in the dark

Application Information

  1. Apply one drop (approximately 20 μL) of FadeStop™ fluorescent mounting medium onto the coverslip, slide, or chamber slide containing the specimen. The amount of the medium is determined by the size of the specimen. As a general rule, apply just enough to cover the specimen area under the coverslip.
  2. Seal the coverslip with quick-dry nail polish to prevent leakage of the mounting medium. Apply four drops of nail polish to each side of the coverslip to secure the coverslip. Then, seal all the sides of the coverslip with nail polish.
  3. Take images immediately or store the slides at -20°C for up to four months.
Data
  • Hela cells were stained with anti-CTCF antibody and mounted in FadeStop™ fuorescent mounting medium. lmages were taken 1 day (D1), 2 months (M2), and 4 months(M4) after staining using Zeiss LSM 880 confocal laser scanning microscope. Nuclei werestained blue with DAPl. ACTB was stained magenta with Alexa Fluor® 647. Scale bars, 20 um.
  • Hela cells were stained with CTCF antibody and mounted in FadeStop™ fluorescent mounting medium. The slide was stored at -20°C for 1 month before imaging using a ZeissLSM 880 confocal laser scanning microscope. A series of scans were performed to assess thephotobleaching speed of the fluorescent dye. Note that even after 12th can, the image quality was still high. Scale bars, 20 μm.
Hela cells were stained with anti-CTCF antibody and mounted in FadeStop™ fuorescent mounting medium. lmages were taken 1 day (D1), 2 months (M2), and 4 months(M4) after staining using Zeiss LSM 880 confocal laser scanning microscope. Nuclei werestained blue with DAPl. ACTB was stained magenta with Alexa Fluor® 647. Scale bars, 20 um.
Hela cells were stained with CTCF antibody and mounted in FadeStop™ fluorescent mounting medium. The slide was stored at -20°C for 1 month before imaging using a ZeissLSM 880 confocal laser scanning microscope. A series of scans were performed to assess thephotobleaching speed of the fluorescent dye. Note that even after 12th can, the image quality was still high. Scale bars, 20 μm.
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