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Key Documents

T5030

Sigma-Aldrich

Solution saline tamponnée au Tris

tablet

Synonyme(s) :

TBS

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About This Item

Numéro MDL:
Code UNSPSC :
12161700
Nomenclature NACRES :
NA.25

product name

Solution saline tamponnée au Tris, tablet

Forme

tablet

Niveau de qualité

Application(s)

diagnostic assay manufacturing

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Application

Tris Buffered Saline Tablets are suitable for use in immunoassay procedures.
It may be used in the following studies:
  • Immunogold-silver staining (IGSS) method to investigate the immunoglobulins in reactive human tonsil.
  • To study the aggregation of purified samples of α-synuclein.
  • As buffer in Western Blot analysis.
  • Time resolved fluoroimmunoassay.
  • As buffer in light microscopic immunohistochemistry.

Reconstitution

One tablet dissolved in 15 mL of deionized water yields 0.05 M Tris and 0.15 M sodium chloride, pH 7.6, at 25 °C.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Kazim SF, Blanchard J, Dai CL, et al.
Neurobiology of Disease, 71, 110-130 (2014)
A J Maniotis et al.
The American journal of pathology, 155(3), 739-752 (1999-09-17)
Tissue sections from aggressive human intraocular (uveal) and metastatic cutaneous melanomas generally lack evidence of significant necrosis and contain patterned networks of interconnected loops of extracellular matrix. The matrix that forms these loops or networks may be solid or hollow.
Muhammad Atteya et al.
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J E Meredith et al.
Molecular biology of the cell, 4(9), 953-961 (1993-09-01)
Programmed cell death (PCD) or apoptosis is a naturally occurring cell suicide pathway induced in a variety of cell types. In many cases, PCD is induced by the withdrawal of specific hormones or growth factors that function as survival factors.
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ACS chemical biology, 14(7), 1611-1618 (2019-07-10)
Lectin-carbohydrate interactions can be exploited in ultrasensitive biochemical recognition or medical diagnosis. For this purpose, besides the high specificity of the interactions, an appropriate methodology for their quantitative and detailed characterization is demanded. In this work, we determine the unbinding

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