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Protamine-Agarose

saline suspension

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About This Item

Número MDL:
Código UNSPSC:
41106500

Formulario

saline suspension

Matriz

Cross-linked 4% beaded agarose

activación de la matriz

cyanogen bromide

unión a la matriz

amino

espaciador de matriz

1 atom

capacidad

~50 μg/mL binding capacity (DNA)

temp. de almacenamiento

2-8°C

Aplicación

Protamine-agarose is used in protein chromatography, affinity chromatography and specialty resins. Protamine-agarose has been used to determine that Pichia pastoris (methylotrophic yeast) provides a convenient heterologous system for the production of recombinant subunits of human type 2A protein phosphatase (PP2A). Protamine-agarose has also been used to purify and characterize a novel protamine kinase in HL60 cells as well as to study myocardial infarction.

Forma física

Suspension in 0.5 M NaCl containing 0.02% thimerosal

Cláusula de descargo de responsabilidad

For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.

Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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I M Helander et al.
European journal of biochemistry, 163(1), 51-55 (1987-02-16)
The ability of agarose-linked protamine to bind Salmonella typhimurium lipopolysaccharides was investigated. Radioactively labelled lipopolysaccharides were isolated both from a smooth strain (SH6749, labelled with [14C]galactose) and from a rough strain (SH5014, lipopolysaccharide chemotype Rb2, labelled with [3H]acetate). From 50-micrograms
M Junco et al.
FEBS letters, 263(1), 169-171 (1990-04-09)
Protein kinase C (PKC) and its proteolysis-derived protein kinase independent of Ca2+ and phospholipids (PKM), were purified from rat brain. By using histone H1 and protamine as substrates, we assayed the effect of several inhibitors of PKC and PKM. The
S Shibata et al.
Journal of biochemistry, 112(4), 552-556 (1992-10-01)
Calphobindins (CPBs, placental annexins) are intracellular Ca(2+)- and phospholipid-dependent proteins like protein kinase C [EC 2.7.1.37]. We investigated the inhibitory effects of calphobindins on the protein kinase C activity in vitro. CPB I inhibited the protein kinase C activity for
V B Lokeshwar et al.
The Journal of biological chemistry, 264(32), 19318-19326 (1989-11-15)
Treatment of Swiss mouse 3T3 cells and human epidermoid carcinoma A431 cells with protamine at 37 degrees C increased the 125I-epidermal growth factor (EGF) binding activity at 4 degrees C. The effect of protamine on the increase of 125I-EGF binding
Bruce M Brown et al.
Biochemistry, 41(46), 13526-13538 (2002-11-13)
In steps of protein purification of bovine retinal protein phosphatase 2A (PP2A), phosducin dephosphorylation activity peaks coelute with a PP2A enzyme complex, shown by peptide sequence analysis to contain a B' subunit, B56 epsilon. Other PP2A complexes with a slightly

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