FSB Solution

FSB Solution

Catalog Number:
IAR1108407DOJ
Mfr. No.:
F308-10
Price:
$661
  • Size:
    100 ul
    Quantity:
    Add to Cart:
      • Overview
        • Amyloidosis, a disease which has been identified as a particular disorder by the Japanese Ministry of Health, is an illness that involves an abnormal protein called amyloid that has a β sheet structure, aggregates in fibers, and is deposited on the outside of internal organs and systems, inhibiting the function of those organs and systems. Disorders among many Japanese include immunocytic amyloidosis (AL amylodosis), responsive AA amyloidsis, familial amyloid polyneuropathy (FAP), and dialysis amyloidsis (DRA). It is estimated that there are hundreds of patients throughout Japan. The proteins that cause amyloidosis can be largely divided into two groups: amylids that are deposited in various organs throughout the body (systemic amyloidosis) such as the disorders listed above, and [ amyloids that are deposited in a particular organ, such as the brain in the case of Alzheimer’s disease (localized amyloidosis). The dye 1-Bromo-2,5-bis(3-carboxy-4-hydroxystyryl)benzene (BSB) has been used for detecting amyloids because of its high affinity with amyloid β peptide (Aβ), the amyloid associated with Alzheimer’s disease.

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      • Properties
        • Molecular Formula
          C24H17FO6
          Molecular Weight
          420.39
          Appearance
          Pale yellow to yellowish brown liquid
          Storage
          0-5°C, protect from light
          Shipping
          ambient temperature

          * For research use only

      • Applications
        • Application
          Alzheimer Disease Research
          Application Description
          Protocol

          1. Add 50% EtOH to the product and dilute to concentration of 0.01~0.0001% FSB solution.

          2. Soak a slice in FSB stain for 30 minutes. After soaking the slice in saturated lithium carbonate, wash with 50% EtOH

          3. Detect stained area under UV light (V excitation)
      • Reference
        • 1) K. Sato, et al., Fluoro-substituted and 13C-labeled styrylbenzene derivatives for detecting brain amyloid plaques. Eur J Med Chem. 2004;39:573-578.

          2) M. Higuchi, et al., 19F and 1H MRI detection of amyloid β plaques in vivo. Nature Nurosci. 2005;8:527-533.

          3) M. Yamamoto, et al., Interferon-γ and Tumor Necrosis Factor-α Regulate Amyloid-β Plaque Deposition and β-Secretase Expression in Swedish Mutant APP Transgenic Mice. Am J Pathol. 2007;170:680-692.

          4) J. Maeda, et al., Longitudinal, Quantitative Assessment of Amyloid, Neuroinflammation, and Anti-Amyloid Treatment in a Living Mouse Model of Alzheimer’s Disease Enabled by Positron Emission Tomography. J Neurosci. 2007;27:10957-10968.

          5) A. Velasco, et al., Detection of filamentous tau inclusions by the fluorescent Congo red derivative FSB [(trans,trans)-1-fluoro-2,5-bis(3-hydroxycarbonyl-4-hydroxy)styrylbenzene]. FEBS Lett. 2008;582:901-906.

          6) B. Ji, et al., Imaging of Peripheral Benzodiazepine Receptor Expression as Biomarkers of Detrimental versus Beneficial Glial Responses in Mouse Models of Alzheimer’s and Other CNS Pathologies. J Neurosci. 2008;28:12255-12267..

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