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Principaux documents

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HT60

Sigma-Aldrich

Amyloid Stain, Congo Red

Synonyme(s) :

Puchtler’s Modification for Amyloid

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About This Item

Code UNSPSC :
41116121
Nomenclature NACRES :
NA.47

Durée de conservation

Expiry date on the label.

IVD

for in vitro diagnostic use

dilution

(for histology)

Application(s)

hematology
histology

Température de stockage

room temp

Principe

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

Composants de kit seuls

Réf. du produit
Description
  • Congo Red Solution (kit only) 500 mL
  • Sodium Chloride Solution, Alcoholic (kit only) 500 mL
  • Sodium Hydroxide Solution (kit only) 2 x 12

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

R8382

Reagent Alcohol, used for histology tissue preparation

MHS80

Mayer′s Hematoxylin Solution

MHS1

Mayer′s Hematoxylin Solution

GHS3128

Hematoxylin Solution, Gill No. 3

P0425

Poly-Prep Slides, poly-L-lysine coated glass slides

MHS16

Mayer′s Hematoxylin Solution

GHS316

Hematoxylin Solution, Gill No. 3

MHS128

Mayer′s Hematoxylin Solution

GHS380

Hematoxylin Solution, Gill No. 3

S4651

Silane-Prep Slides, glass slides coated with silane (aminoalkylsilane).

GHS332

Hematoxylin Solution, Gill No. 3

MHS32

Mayer′s Hematoxylin Solution

Pictogrammes

FlameHealth hazardCorrosion
GHS02,GHS08,GHS05

Mention d'avertissement

Danger

Mentions de danger

H225,H290,H315,H319,H350

Classification des risques

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

Code de la classe de stockage

3 - Flammable liquids

Point d'éclair (°F)

57.2 °F - closed cup

Point d'éclair (°C)

14.0 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
0000381396
0000353832
0000353832
0000381396
SLCK3798

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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
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
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
Brian O'Nuallain et al.
The Journal of biological chemistry, 279(17), 17490-17499 (2004-01-31)
Over residues 15-36, which comprise the H-bonded core of the amyloid fibrils it forms, the Alzheimer's disease plaque peptide amyloid beta (Abeta) possesses a very similar sequence to that of another short, amyloidogenic peptide, islet amyloid polypeptide (IAPP). Using elongation
Tsung-Ting Tsai et al.
Journal of orthopaedic surgery and research, 12(1), 194-194 (2017-12-23)
Dialysis-related destructive spondyloarthropathy caused by beta-2 microglobulin (β2M) amyloid deposits in intervertebral discs is a major burden for patients undergoing long-term dialysis. This study aimed to quantify the presence of β2M amyloid deposits in the intervertebral disc tissue of such
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