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Merck

507861

PANSORBIN® Cells, Standardized

Synonyme(s) :

Cell standard

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A propos de cet article

NACRES:
NA.42
UNSPSC Code:
41116133
Manufacturer/tradename:
Calbiochem®
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form

liquid

contains

0.1% sodium azide as preservative

manufacturer/tradename

Calbiochem®

storage condition

do not freeze

capacity

≥2 mg/mL binding capacity

shipped in

ambient

Quality Level

General description

Heat-killed, formalin-fixed Staphylococcus aureus cells (Cowan I strain) that bear a high cell-surface density of protein A and have been pickled by the method of Kessler. Useful as a solid-phase IgG-binding reagent due to the high-affinity interaction of protein A with the Fc domain of IgG. PANSORBIN cells work best when the antibody is human (IgG1, IgG2, IgG4), rabbit IgG (all isotypes), or mouse (IgG2a, IgG2b, IgG3).
PANSORBIN Cells are heat-killed, formalin fixed Staphylococcus aureus cells that have a coat of protein A and have been pickled by the method of Kessler. Useful for mitogenic stimulation of B lymphocytes and for immunoprecipitation.

Application

Most common applications include immunoprecipitation and mitogenic stimulation of B lymphocytes.

Physical form

Supplied as a ≥10% (w/v) Staphylococcus aureus cell suspension in PBS, 0.1% sodium azide, pH 7.2.

Other Notes

Kierszenbaum, F., et al. 1991. Immunology74, 317.
Meikle, P.J., et al. 1991. J. Biol. Chem.266, 22569.
Ezaki, O., et al. 1989. Biochem. Biophys. Res. Commun. 159, 1368.
Murakami, H., et al. 1988. Biochem. J.256, 917.
Kessler, S.W. 1975. J. Immunol. 115, 1617.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
PANSORBIN is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Classe de stockage

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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S Ebner et al.
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Use of recombinant vaccinia virus vectors for cell biology.
O A Weisz et al.
Methods in cell biology, 43 Pt A, 137-159 (1994-01-01)
Peifang Sun et al.
Methods in molecular biology (Clifton, N.J.), 1808, 187-196 (2018-06-30)
Dengue envelope (E) protein is a dominant antigen for vaccine development and E-based vaccines have shown partial or full protection against live-virus challenge in non-human primates. Generally, T cell responses can be investigated with peptides. However, hundreds of over-lapping peptides
Menaka D Hapugoda et al.
Clinical and vaccine immunology : CVI, 14(11), 1505-1514 (2007-09-28)
The resurgence of dengue (DEN) virus infections in the last few decades coupled with the lack of a preventive vaccine and specific antiviral drugs has jointly contributed to making this a significant global public health problem. Currently, symptomatic supportive treatment
K E Reed et al.
Methods in molecular medicine, 19, 331-342 (1999-01-01)
Heterologous expression systems have been widely used to study hepatitis C virus (HCV) proteins in lieu of an efficient method for establishing HCV infections in cell culture. Studies of HCV polyprotein processing in both mammalian-cell-based and cell-free expression systems have

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