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Merck
CN
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MAB8920

Sigma-Aldrich

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

ascites fluid, Chemicon®, from mouse

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别名:
Rubeola
UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物来源

mouse

质量水平

300

抗体形式

ascites fluid

抗体产品类型

primary antibodies

克隆

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

种属反应性

human

制造商/商品名称

Chemicon®

技术

immunofluorescence: suitable

同位素/亚型

IgG

运输

wet ice

特异性

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

免疫原

Epitope: hemagglutinin & matrix protein

应用

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

外形

Ascites fluid, no preservatives.

储存及稳定性

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

法律信息

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

免责声明

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.

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°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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