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Untitled - D Ank Unlimited

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molecular hybridization probe 503 monoclonal antibody (mAb)<br />

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G F E D C B A<br />

Example of high resolution DRBI typing using sequence-specific primer<br />

methodology. Far left column shows molecular weight ladder of known<br />

base pairs for base pair sizing.<br />

perfectly matched primer pair results in an amplification<br />

product, whereas a mismatch at the 3′ end primer pair will<br />

not provide an amplification product. A positive result, i.e.,<br />

amplification, defines the specificity of the DNA sample.<br />

The PCR amplification step provides the basis for identifying<br />

polymorphism. The post amplification processing of the<br />

sample consists only of a simple agarose gel electrophoresis<br />

to detect the presence or absence of amplified product. DNA<br />

amplified fragments are visualized by ethidium bromide<br />

staining and exposure to UV light. A separate technique<br />

detects amplified product by color fluorescence. The primer<br />

pairs are selected in such a manner that each allele should<br />

have a unique reactivity pattern with the panel of primer<br />

pairs employed. Appropriate controls must be maintained.<br />

Mollusks and arthropods.<br />

molecular hybridization probe<br />

A molecule of nucleic acid labeled with a radionuclide or<br />

fluorochrome that can reveal the presence of complementary<br />

nucleic acid through molecular hybridization such as in situ.<br />

molecular mimicry<br />

The sharing of antigenic determinants or epitopes between<br />

cells of an immunocompetent host and a microorganism<br />

may lead to pathologic sequelae if antibodies produced<br />

against the microorganism combine with antigens of self<br />

and lead to immunologic injury. <strong>Ank</strong>ylosing spondylitis and<br />

rheumatic fever are examples. Immunologic cross reactivity<br />

between a viral antigen and a self antigen or between<br />

a bacterial antigen such as streptococcal M protein and<br />

human myocardial sarcolemmal membranes may lead to<br />

tissue injury. Cross reactive epitopes involving molecular<br />

mimicry may be sequential (common amino acid determinants<br />

between host and pathogen) or conformational (cross<br />

reactivity to chemical moieties such as glycans, phosphates,<br />

or sulfates that reveal a specific tertiary configuration and<br />

electrostatic potential). Rothbard epitopes, which are common<br />

cognate T cell epitopes, may also induce cross reactive<br />

T lymphocyte responses. Molecular mimicry may also be<br />

observed in the idiotype network in which anti-Id antibodies<br />

can generate a mirror image of the original antigen.<br />

mollusks and arthropods<br />

Mollusks and arthropods fail to manifest graft rejection even<br />

though they possess significant humoral factors including what<br />

may be the most primitive alternative complement pathway<br />

components that may provide resistance to selected parasites.<br />

Moloney test<br />

Diphtheria toxoid is injected intradermally, and the skin<br />

response is observed to determine whether the subject is<br />

hypersensitive to diphtheria prophylactic substances.<br />

monoclonal<br />

Derived from a single clone.<br />

monoclonal antibody (mAb)<br />

Monoclonal antibodies are synthesized by a single clone of<br />

B lymphocytes or plasma cells and have identical structure<br />

and antigen specificity. The first to be observed were produced<br />

by malignant plasma cells in patients with multiple<br />

myeloma and associated gammopathies. The identical<br />

copies of the antibody molecules produced contain only<br />

one class of heavy chain and one type of light chain. Kohler<br />

and Millstein in the mid-1970s developed B lymphocyte<br />

hybridomas by fusing an antibody-producing B lymphocyte<br />

with a mutant myeloma cell that was not secreting antibody.<br />

The B lymphocyte product provided the specificity,<br />

whereas the myeloma cell conferred immortality on the<br />

hybridoma clone. Today monoclonal antibodies (mAbs) are<br />

produced in large quantities against a plethora of antigens<br />

for use in diagnosis and sometimes treatment. mAbs are<br />

homogeneous and widely employed in immunoassays,<br />

single antigen identification in mixtures, delineation of<br />

cell surface molecules, and assays of hormones and drugs<br />

in serum, among other uses. Since the responses to some<br />

immunogens are inadequate in mice, monoclonal antibodies<br />

have also been generated using rabbit cells. Monoclonal<br />

antibodies have been radioactively labeled and used to<br />

detect tumor metastases, to differentiate subtypes of tumors<br />

with monoclonal antibodies against membrane antigens or<br />

intermediate filaments, to identify microbes in body fluids,<br />

and for circulating hormone assays. mAbs may be used to<br />

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