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SeroMP™ Recombinant IgA

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  • ¥3200
  • 萨卫亚
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  • 2025年12月14日
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      96T

    Intended Use
    SeroMP™ Recombinant IgA kit is a semi-quantitative
    Enzyme Linked Immunosorbent assay (ELISA) for the
    determination of species specific IgA antibodies to
    Mycoplasma pneumoniae in human serum.
    Savyon® SeroMP™ Recombinant IgA kit is used as an aid in
    the diagnosis of Mycoplasma pneumoniae infection.
    For In Vitro Diagnostic Use.
    Introduction
    M. pneumoniae is a common cause of community-acquired
    pneumonia, often characterized by gradual onset of
    headache, fever, malaise and, most typically, dry cough. M.
    pneumoniae is common in all age groups, however, it is
    most common in the first two decades of life and is rare in
    children under the age of four. It has been reported as the
    cause of up to 30% of all pneumonia cases (2).
    M. pneumoniae has also been associated with non
    respiratory diseases as meningitis, encephalitis, pancreatitis,
    sensorineural hearing loss, and acute brainstem syndrome
    (5).
    Due to its common occurrence, one should consider M.
    pneumoniae in all cases of pneumonia, but being the same
    symptoms for different agents, additional diagnostic tools,
    such as serological tests, are required (3).
    The ELISA technique is sensitive, specific and enables a
    differential determination of specific IgG, IgA and IgM antibodies (6).

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    相关实验
    • Expression of IgA Molecules in Mammalian Cells

      antibodies is the lack of well established production and purification technologies. Here, we describe protocols to produce and purify recombinant chimeric IgA antibodies irrespective of their antigen specificity. Resulting antibodies were monomeric, fully

    • Recombinant Baculovirus Isolation

      Although there are several different methods available of making recombinant baculovirus expression vectors (reviewed in Chapter 3), all require a stage in which insect cells are transfected with either the virus genome alone (Bac-to-Bac�

    • Purification of Recombinant Poly(ADP-Ribose) Polymerases

      extract are separated on a Heparine Sepharose column. The PARP-containing fractions are then affinity purified on a 3-aminobenzamide Sepharose chromatographic step. The last contaminants and the 3-methoxybenzamide used to elute the PARP from the previous

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