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HT60

Amyloid Stain, Congo Red

Sinonimo/i:

Puchtler’s Modification for Amyloid

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Informazioni su questo articolo

NACRES:
NA.47
UNSPSC Code:
41116121
Prezzi e disponibilità al momento non sono disponibili
Servizio Tecnico
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shelf life

Expiry date on the label.

Quality Level

IVD

for in vitro diagnostic use

dilution

(for histology)

application(s)

hematology
histology

storage temp.

room temp

Biochem/physiol Actions

Amyloid protein is detected in tissue with Congo red, a metachromatic stain. Staining is intensified by pretreatment of tissue with alkaline sodium chloride.

Solo come componenti del kit

N° Catalogo
Descrizione

  • Congo Red Solution (kit only) 500 mL

  • Sodium Chloride Solution, Alcoholic (kit only) 500 mL

  • Sodium Hydroxide Solution (kit only) 2 x 12

related product

N° Catalogo
Descrizione
Determinazione del prezzo

signalword

Danger

Hazard Classifications

Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Met. Corr. 1 - Skin Irrit. 2

Classe di stoccaggio

3 - Flammable liquids

flash_point_f

57.2 °F - closed cup

flash_point_c

14.0 °C - closed cup


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J Grayson Richards et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 23(26), 8989-9003 (2003-10-03)
Transgenic mice, expressing mutant beta-amyloid precursor proteins (betaAPPs), have lead to a better understanding of the pathophysiological processes in Alzheimer's disease (AD). In many of these models, however, the temporal development of cognitive decline and the relationship to Abeta deposition
Fubing Ouyang et al.
Brain pathology (Zurich, Switzerland), 30(1), 165-178 (2019-07-07)
Conflicting evidence exists regarding whether focal cerebral infarction contributes to cerebral amyloid-β (Aβ) deposition, as observed in Alzheimer's disease. In this study, we aimed to evaluate the presence of Aβ deposits in the ipsilateral thalamus and hippocampus 12 months post-stroke
Laurence Ozmen et al.
Neuro-degenerative diseases, 2(6), 284-298 (2006-08-16)
Most of the transgenic mice generated to model Alzheimer's disease express human amyloid precursor protein (APP) mutants alone or in conjunction with presenilin mutants. We have generated a mouse model by overexpressing human BACE and human APP with the V717F
Lei Wang et al.
PLoS biology, 6(8), e195-e195 (2008-08-08)
Protein aggregation is a process in which identical proteins self-associate into imperfectly ordered macroscopic entities. Such aggregates are generally classified as amorphous, lacking any long-range order, or highly ordered fibrils. Protein fibrils can be composed of native globular molecules, such
Antje Willuweit et al.
Frontiers in neuroscience, 15, 699926-699926 (2021-10-22)
Alzheimer's disease (AD) is characterized by formation of amyloid plaques and neurofibrillary tangles in the brain, which can be mimicked by transgenic mouse models. Here, we report on the characterization of amyloid load in the brains of two transgenic amyloidosis

Protocolli

A stem cell culture protocol to generate 3D NSC models of Alzheimer’s disease using ReNcell human neural stem cell lines.

Numero articolo commerciale globale

SKUGTIN
HT60-1KT04061838261908

Questions

1–2 of 2 Questions  
  1. Are there any protocols/literature available that have adapted Congo Red staining for cell cultures?

    1 answer
    1. There is no published procedure for using the HT60 kit for cultured cells, and such usage is regarded as off-label. The Congo Red Amyloid kit was designed for tissue sections, but most histological procedures can be used on cultured adherent cells. Specific considerations are mentioned for the thickness of cells and the use of a polarized microscope. Congo Red staining has specific requirements for cells to be stated at a certain thickness. If the cells are within the 6-12 micron range, no major adjustments to the protocol are expected. However, if the cells are extremely small or large, this might be an issue. Additionally, it is advised to utilize a polarized microscope for Congo Red staining, as it can be somewhat nonspecific when using a bright field microscope or an inverted microscope. Not everything that stains red under a light microscope with Congo Red is necessarily amyloid. Apple green staining with polarized microscopy is considered specific for Congo Red. It's important to note that not everything that stains red with Congo Red can automatically be assumed to be amyloid. Adapting a bright field microscope to use the polarized filters necessary for polarized microscopy is possible, but it is uncertain if this is possible when using an inverted microscope.

      Due to possible size variation, it is recommended to stain a series of slides if possible. Starting with the times stated in the pdf file is advised, and the staining time may be varied depending upon the thickness or size of the cultured cells. Trying both shortened and extended times depending upon the results obtained is also recommended.

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  2. What kind of mounting media should be used - organic or aqueous?

    1 answer
    1. Most histology procedures will instruct to mount in either a synthetic or an aqueous mounting media. Simply rinse three times in ethanol after coming out of the Alkaline Congo Red working solution. The slides should then be cleared in xylene and mounted. Also, mounting in a synthetic mounting media, such as DPX or other similar type permanent mounting medias can be tried.

      Helpful?

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