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Merck
CN

MAB8253

Anti-Influenza A Antibody, H-1 Antigen, clone 58CE8-1-5

clone 58CE8-1-5, Chemicon®, from mouse

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
58CE8-1-5, monoclonal
Species reactivity:
human
Application:
IF
Citations:
1
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biological source

mouse

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

58CE8-1-5, monoclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

immunofluorescence: suitable

isotype

IgG1

shipped in

wet ice

Quality Level

Immunogen

Epitope: H-1 Antigen
Influenza blend

Application

Anti-Influenza A Antibody, H-1 Antigen, clone 58CE8-1-5 detects level of Influenza A & has been published & validated for use in IF.
Indirect Immunofluorescence
Research Category
Infectious Diseases
Research Sub Category
Infectious Diseases - Viral

Biochem/physiol Actions

Influenza A H1 antigen. Reacts strongly with the following H1N1 strain: A/Taiwan/1/86

Physical form

Format: Purified
Purified Immunoglobulin.

Liquid in Phosphate buffered saline with 0.1% Sodium Azide, pH 7.4

Preparation Note

Maintain at 2-8°C.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Legal Information

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

Disclaimer

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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存储类别

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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José Francisco Rivera-Benitez et al.
Veterinary microbiology, 184, 31-39 (2016-02-09)
Porcine rubulavirus (PorPV) and swine influenza virus infection causes respiratory disease in pigs. PorPV persistent infection could facilitate the establishment of secondary infections. The aim of this study was to analyse the pathogenicity of classic swine H1N1 influenza virus (swH1N1)

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