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Untitled - D Ank Unlimited

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light chain deficiencies 452 light scatter<br />

Fas Is a member of the tumor necrosis factor (TNF) receptor superfamily<br />

and contains a cytoplasmic death domain (DD) required for Induction of<br />

apoptosis. Fas ligand (FasL)-Induced receptor trimerization aggregates<br />

the DD of Fas and recruites the adaptor protein FADD and procaspase 8.<br />

Following activation of caspase 8, the DD-Induced complex can trigger<br />

subsequent events of apoptosis.<br />

Ligh polypeptide chains of immunoglobulins that are fastened to<br />

heavy chains through disulfide bonds and are found in all classes of<br />

immunoglobulin.<br />

chains are designated κ and λ. An individual immunoglobulin<br />

molecule possesses two light chains that are κ or λ, but<br />

never a combination of both. The types of light polypeptide<br />

chains occur in all five immunoglobulin classes. Each light<br />

chain has an N terminal V region that constitutes part of the<br />

antigen-binding site of the antibody molecule. The C region<br />

or constant terminal reveals no variation except for the Km<br />

and Oz allotype markers in humans.<br />

light chain deficiencies<br />

The ratio of κ to λ light chains may be altered in individuals<br />

with immunodeficiencies. κ Chain deficiency has<br />

been associated with respiratory infections, megaloblastic<br />

anemia, and diarrhea. It has also been associated with<br />

achlorhydria and pernicious anemia and has even been seen<br />

in cases of malabsorption, diabetes, and cystic fibrosis. T<br />

cell function in all these cases was within normal limits,<br />

with only defective B cell immunity observed. Abnormal<br />

κ and λ light-chain ratios are secondary findings in certain<br />

diseases; they may also act as primary etiologic agents.<br />

light chain disease<br />

A paraproteinemia also known as Bence–Jones myeloma<br />

that comprises one fifth of all myelomas. Excess monoclonal<br />

light chains are produced. These are linked to renal<br />

amyloidosis and renal failure as a consequence of blockage<br />

of tubules by certain Bence–Jones proteins. Four fifths of<br />

patients have monoclonal light chains in the blood circulation,<br />

and 60% have diminished γ globulin and lytic lesions<br />

of the bone. The λ type is usually more severe than the κ<br />

type. Patients with light chain disease experience a worse<br />

course than patients with IgA or IgG myelomas.<br />

light chain subtype<br />

The subdivision of a type of light polypeptide chain based<br />

on its primary or antigenic structure that appears in all<br />

members of a species. Subtype differences distinguish light<br />

chains that share a common type. These relatively minor<br />

structural differences are located in the light chain constant<br />

region. Oz + , Oz – , Kern + , and Kern – markers represent subtypes<br />

of λ light chains in humans.<br />

light chain type<br />

The classification of immunoglobulin light chains based<br />

on their primary or antigenic structures. Two types of light<br />

chain have been described and are designated κ and λ. Two κ<br />

chains or two λ chains, never one of each, are present in each<br />

monomeric immunoglobulin subunit of vertebrate species.<br />

Forward scatter—diffracted light<br />

Related to cell surface area<br />

Incident<br />

Light<br />

Source<br />

Right angle light detector<br />

α cell complexity<br />

Detected along axis of incident light in the forward direction<br />

Side Scatter—reflected and refracted light<br />

Related to cell granularity and complexity<br />

Detected at 90° to the laser beam<br />

Forward light detector<br />

α cell surface area<br />

Properties of forward scatter light and side scatter light are measured by<br />

observing how light disperses when a laser hits a cell.<br />

light scatter<br />

Light dispersion in any direction that may be useful for<br />

studying cells by flow cytometry. A cell passing through a<br />

laser beam absorbs and scatters light. Fluorochrome staining<br />

of cells permits absorbed light to be emitted as fluorescence.<br />

Forward angle light scatter permits identification of a cell in<br />

flow and determination of its size. If higher angle light scatter<br />

is added, certain specific cell populations may also be identified.<br />

Light scatter measured at 90° to the laser beam and

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