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Merck
CN

MAB8920

Anti-Measles Blend Antibody, hemagglutinin & matrix protein, clones CV1, CV4, CV8, CV9

ascites fluid, Chemicon®, from mouse

别名:

Rubeola

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
CV1, monoclonal, CV4, monoclonal, CV8, monoclonal, CV9, monoclonal
Species reactivity:
human
Application:
IF
Citations:
2

主要文件

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biological source

mouse

antibody form

ascites fluid

antibody product type

primary antibodies

clone

CV1, monoclonal, CV4, monoclonal, CV8, monoclonal, CV9, monoclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

immunofluorescence: suitable

isotype

IgG

shipped in

wet ice

Quality Level

300

Immunogen

Epitope: hemagglutinin & matrix protein

Application

Anti-Measles Blend Antibody, hemagglutinin & matrix protein, clones CV1, CV4, CV8, CV9 detects level of Measles Blend & has been published & validated for use in IF.
Culture Confirmation.

Indirect Immunofluorescence at 1:100-1000.

Final working dilutions must be determined by end user.
Research Category
Infectious Diseases
Research Sub Category
Infectious Diseases - Viral

Biochem/physiol Actions

Recognizes the measles hemagglutinin and the matrix protein by indirect immunofluorescence.

Physical form

Ascites fluid, no preservatives.

Preparation Note

Maintain at -20°C in aliquots for up to 12 months. Avoid repeated freeze/thaw cycles.

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 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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G J Nuovo et al.
PCR methods and applications, 2(2), 117-123 (1992-11-01)
We describe a technique, called reverse transcriptase (RT) in situ PCR, whereby RNA may be nonisotopically detected in fixed cells when amplified by PCR after cDNA synthesis by RT. RT in situ PCR using primers specific for the measles virus
K G Mansfield et al.
Veterinary pathology, 51(1), 110-126 (2013-10-31)
Molecular localization techniques remain important diagnostic and research tools for the pathologist evaluating nonhuman primate tissues. In situ hybridization and immunohistochemistry protocols have been developed for many important pathogens of nonhuman primates, including RNA and DNA viruses, prions, and bacterial

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