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MAB8256

Sigma-Aldrich

Anti-Influenza A Antibody, H1N1 Antigen, clone 9B3.2

ascites fluid, clone 9B3.2, Chemicon®

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About This Item

UNSPSC-Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Biologische Quelle

mouse

Qualitätsniveau

Antikörperform

ascites fluid

Antikörper-Produkttyp

primary antibodies

Klon

9B3.2, monoclonal

Speziesreaktivität

human

Hersteller/Markenname

Chemicon®

Methode(n)

immunofluorescence: suitable

Isotyp

IgG2a

Versandbedingung

wet ice

Spezifität

Influenza A H1N1 antigen.
• Reacts strongly with all H1N1 strains tested including Beijing, A/ Texas /36/91, A/Berkeley/1/98, A/HongKong/503/97, A/Nanchang /16A/98,A/PR/8/34, New Caledonia strain, and A/California/7/2009.
• No reactivity shown to Influenza B strains.

Immunogen

Epitope: H1N1 Antigen
Influenza blend

Anwendung

Research Category
Infektionskrankheiten
Research Sub Category
Virale Infektionskrankheiten
Anti-Influenza A Antibody, H1N1 Antigen, clone 9B3.2 is an antibody against Influenza A for use in IF.
Indirect Immunofluorescence : 1/32

Physikalische Form

Ascites

Lagerung und Haltbarkeit

Maintain at -20°C. Avoid repeated freeze/thaw cycles.

Rechtliche Hinweise

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Haftungsausschluss

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Lagerklassenschlüssel

10 - Combustible liquids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Asami Makino et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 31(4), 1301-1322 (2016-08-06)
We identified a novel, nontoxic mushroom protein that specifically binds to a complex of sphingomyelin (SM), a major sphingolipid in mammalian cells, and cholesterol (Chol). The purified protein, termed nakanori, labeled cell surface domains in an SM- and Chol-dependent manner
Brian J Morrison et al.
Journal of virological methods, 248, 7-18 (2017-06-19)
This study describes an antibody-dependent NK cell degranulation assay, as a biomarker to assess antibody-dependent cellular cytotoxicity (ADCC) response in influenza plasma and for antibody therapies against influenza infection. The concentration of neutralizing antibodies (NAbs) against the hemagglutinin receptor of
Sreekumar Othumpangat et al.
Pathogens (Basel, Switzerland), 12(1) (2023-01-22)
Understanding the host response to influenza A virus (IAV) infection is vital for developing intervention strategies. The primary barriers for invading respiratory pathogens are the respiratory tract epithelial cells and antimicrobial proteins generated by these cells. The antimicrobial peptide, β-defensin-1
Rapid typing, subtyping and RNA quantification of influenza virus type A strains in respiratory secretions.
Elena Percivalle,Francesca Rovida,Antonio Piralla,Vanina Rognoni,Maurizio Zavattoni et al.
The New Microbiologica null
Amani Audi et al.
Frontiers in microbiology, 11, 612-612 (2020-05-20)
Influenza A virus (IAV) is a major human respiratory pathogen causing annual epidemics as well as periodic pandemics. A complete understanding of the virus pathogenesis and host factors involved in the viral lifecycle is crucial for developing novel therapeutic approaches.

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