|Immunogen||Purified M1 protein, Influenza A-Phillipines (H3N2)|
|Purification||IgG fraction covalently coupled with high purity Isomer I of fluorescein isothiocyanate. Care is taken to ensure complete removal of any free fluorescein from the final product.|
|Target/Specificity||Influenza A matrix protein (M1). Recognizes the M1 protein for any strain of Influenza A. Conservation of the matrix protein sequence between hemagglutinin/Neuraminidase typed strains. Does not react with the M2 matrix protein. Does not react with HEp-2 cells by indirect immunofluorescence. Does not react with Influenza B, Adenovirus, Respiratory syncytial virus and Parainfluenza viruses (1-3).|
|Preservative||0.1% Sodium azide|
|Storage||Short-term (up to 6 months) store at 2-8°C under subdued light. Long term, aliquot and store at -20°C. Avoid multiple freeze/thaw cycles.|
|Precautions||Goat Antibody to Influenza a Virus Matrix Protein M1 Fluorescein conjugated is for research use only and not for use in diagnostic or therapeutic procedures.|
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Provided below are standard protocols that you may find useful for product applications.
The references listed below are for research purposes only.1. Hui, Eric Ka-Wai, et al., (2003), “Conserved cysteine and histidine residues in the putative zinc finger motif of the influenza A virus M1 protein are not critical for influenza virus replication”, Journal of General Virology, 84, 3105-3113.2. Hui, Eric Ka-Wai, et al., (2004), “Inhibition of influenza virus matrix (M1) protein expression and virus replication by U6 promoter-driven and lentivirus-mediated delivery of siRNA”, Journal of General Virology, 85, 1877-1884.
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