产品名称
Anti-Measles Blend Antibody, matrix protein, clones CV8, CV9, Chemicon®, from mouse
biological source
mouse
antibody form
purified antibody
antibody product type
primary antibodies
clone
CV8, monoclonal
CV9, monoclonal
species reactivity
human
manufacturer/tradename
Chemicon®
technique(s)
immunofluorescence: suitable
isotype
IgG
shipped in
wet ice
Quality Level
Application
Detect Measles Blend using this Anti-Measles Blend Antibody, matrix protein, clones CV8, CV9 validated for use in IF.
Indirect Immunofluorescence
Final working dilutions must be determined by end user.
Final working dilutions must be determined by end user.
Research Category
Infectious Diseases
Infectious Diseases
Research Sub Category
Infectious Diseases - Viral
Infectious Diseases - Viral
Biochem/physiol Actions
Recognizes the measles matrix protein by indirect immunofluorescence.
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.
Immunogen
Epitope: matrix protein
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Physical form
Format: Purified
In 0.02M PB with 0.25M NaCl containing 0.1% sodium azide, pH 7.6.
Preparation Note
Maintain at 2-8°C in aliquots for up to 12 months.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Elements in the canine distemper virus M 3' UTR contribute to control of replication efficiency and virulence.
Anderson, DE; Castan, A; Bisaillon, M; von Messling, V
Testing null
Electron cryotomography of measles virus reveals how matrix protein coats the ribonucleocapsid within intact virions.
Liljeroos, L; Huiskonen, JT; Ora, A; Susi, P; Butcher, SJ
Proceedings of the National Academy of Sciences of the USA null
Full-length sequence analysis of subacute sclerosing panencephalitis (SSPE) virus, a mutant of measles virus, isolated from brain tissues of a patient shortly after onset of SSPE.
Hak Hotta, Kenji Nihei, Yu-ichi Abe, Seiichi Kato, Da-Peng Jiang, Motoko Nagano-Fujii, Kiyonao Sada
Microbiology and Immunology null
Bevan Sawatsky et al.
The Journal of general virology, 97(5), 1066-1076 (2016-01-28)
The amino-terminal cytoplasmic domains of paramyxovirus attachment glycoproteins include trafficking signals that influence protein processing and cell surface expression. To characterize the role of the cytoplasmic domain in protein expression, fusion support and particle assembly in more detail, we constructed
Kento Sakamoto et al.
PLoS pathogens, 19(7), e1011528-e1011528 (2023-07-26)
Subacute sclerosing panencephalitis (SSPE) is a fatal neurodegenerative disease caused by measles virus (MV), which typically develops 7 to 10 years after acute measles. During the incubation period, MV establishes a persistent infection in the brain and accumulates mutations that
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