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SAE0087

Filipin III ready made solution

from Streptomyces filipinensis, 1mg/ml in DMSO based solution

Synonyma:

Filipin III solution

pro zobrazení organizačních a smluvních cen.

Vybrat velikost

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Vám/Skladová položkaDostupnostCena
1 mL
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7 230,00 Kč

O této položce

NACRES:
NA.77
UNSPSC Code:
12352200

7 230,00 Kč


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Quality Segment

assay

≥95% (HPLC)

form

ready-to-use solution

storage condition

protect from light

shipped in

dry ice

storage temp.

−20°C

General description

Filipin III is a polyene macrolide antibiotic and the major component isolated from cultures of S. filipinensis. 1 Due to its ability to fluoresce and bind to cholesterol, Filipin has been widely
used as a probe for sterol location in biological membranes 2 and has been used clinically as a stain for free cholesterol in the study of Type C Niemann-Pick disease. 3 Filipin inhibits prion protein (PrP) endocytosis and causes the release of PrP from the plasma membrane. 4 Filipin III was found to trigger signaling responses in tobacco cells, including a NADPH oxidase-dependent production. 5. The antifungal mechanism of action may be due to altering membrane permeability and associated functions by binding to membrane sterols. Filipin inhibits prion protein (PrP) endocytosis and causes the release of PrP from the plasma membrane.

Application

Filipin has been used in a double staining procedure as a probe for the detection of lipoproteins in polyacrylamide gel and immobilized on nitrocellulose membranes. It is also widely used to localize and quantitate unesterified cholesterol by virtue of a specific fluorescent complex.

Other Notes

  • Filipin III solution is very sensitive to air and light. Upon receipt aliquot and store at -20°C avoid freeze thaw cycles.
  • Filipin III is used in various concentrations depending on the specific protocol used. Dilute 1mg/ml stock solution with appropriate buffer according to the used protocol.
  • Filipin III interaction with cholesterol alters the absorption and fluorescence spectra, for visualization with a fluorescence microscope use excitation at 340-380 nm and emission at 385-470 nm (Filipin fluorescent staining photo-bleaches very rapidly, thus the sample should be analyzed immediately).

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Tato položka
SAE0088SML3001A4487
Quality Level

200

Quality Level

-

Quality Level

100

Quality Level

200

assay

≥95% (HPLC)

assay

≥90% (HPLC)

assay

-

assay

-

form

ready-to-use solution

form

ready-to-use solution

form

liquid

form

liquid, ready-to-use solution

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage condition

protect from light

storage condition

protect from light

storage condition

protect from light

storage condition

-

shipped in

dry ice

shipped in

dry ice

shipped in

-

shipped in

-


Skladovací třída

10 - Combustible liquids

wgk

WGK 1

flash_point_f

188.6 °F

flash_point_c

87 °C



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Lot/Batch Number

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Questions

1–3 of 3 Questions  
  1. Does Filipin III ready made solution require prior fixation, both in flow cytometry and microscopy imaging?

    1 answer
    1. No specific staining protocol is available for this product. Scientific literature indicates that cell fixation is required for both flow cytometry and microscopy imaging when using Filipin III. Please see the link below.
      https://www.nature.com/articles/s41467-023-39640-w.pdf

      Helpful?

  2. Would it be possible to image this product using a DAPI filter (Excitation 377 nm, Emission 447 nm)?

    1 answer
    1. Yes, this material has a fluorescence spectrum similar to DAPI, with excitation at 340-380 nm and emission at 385-470 nm. The images displayed above were acquired using UV filter set (340-380 nm excitation, 40 nm dichroic, 430-nm long pass filter). Please note that Filipin fluorescent staining photo-bleaches very rapidly, thus the sample should be analyzed immediately.

      Helpful?

  3. Any suggestions for addressing white precipitations observed during Filipin staining for endothelial cells, possibly due to DMSO? Also, seeking advice to improve the experiment where most cells were negative for Filipin staining, and only a few were positive while measuring cholesterol content in HUVEC cells.

    1 answer
    1. To address white precipitations observed during Filipin staining for endothelial cells, increasing the amount of DMSO in the final staining solution may be necessary. This can be achieved by diluting the 1 mg/ml Filipin III solution with more DMSO solution to create a 0.5 mg/ml or 0.1 mg/ml concentrated solution prior to staining the samples.
      For improving cholesterol content measurement in HUVEC cells, optimize the working concentration of Filipin and conduct a time-course experiment to enhance staining results. Prompt analysis of stained samples can help prevent photobleaching.

      Helpful?

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