T1763
Trypsin Agarose
buffered aqueous suspension, from bovine pancreas trypsin
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$112.00
50 UNITS
$196.00
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25 UNITS
$112.00
50 UNITS
$196.00
About This Item
Número MDL:
Código UNSPSC:
12352204
eCl@ss:
42020142
NACRES:
NA.54
$112.00
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origen biológico
bovine pancreas (trypsin)
Formulario
buffered aqueous suspension
concentración
≥15 units/mL (packed gel)
Extensión del etiquetado
≥15 units per mL packed gel
Matriz
cross-linked beaded agarose
Condiciones de envío
wet ice
temp. de almacenamiento
2-8°C
Categorías relacionadas
Descripción general
The trypsin molecule has two domains: one is related to the enzyme active site and the tryptophan residues; the other is related to the 8-anilinonaphthalene-1-sulfonate binding.
Trypsin Agarose is an insoluble enzyme product. It is produced by reacting a conventional "soluble" enzyme (trypsin) with an inert base (agarose). This insoluble conjugate retains the activity of the original enzyme. Trypsin bound to agarose are highly stable and maintain denaturing conditions for longer time than the soluble trypsin.[1]
Aplicación
A very active and very stable trypsin agarose derivative has been used to optimize the design of the synthesis of a model dipeptide, benzoylarginine leucinamide. [2] Trypsin has also been used in a study to investigate protonation-state determination in proteins using high-resolution X-ray crystallography. [3]
Otras notas
Insolubilized
Definición de unidad
One unit will hydrolyze 1.0 μmole of BAEE per min at pH 8.0 at 30 °C (titrimetric assay).
Forma física
Suspension in approx. 10 mM acetic acid, pH 3.2
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Órganos de actuación
Respiratory system
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 3
Equipo de protección personal
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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By using very active and very stable trypsin agarose derivatives, we have optimized the design of the synthesis of a model dipeptide, benzoylarginine leucinamide, by two different strategies: (i) kinetically controlled synthesis (KCS), by using benzoyl arginine ethyl ester and
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