Considerable progress has been made in the development of the polarometer. Some improvement in sensitivity has been achieved by changes in optical design and incorporation of a more efficient light source. Keywords UA Reports, Immunology, Antigen-antibody reactions, Chemical analysis, Medical instrumentation, Computer techniques, Fluorescence polarization, IBM 7090, Data processing, Diphtheria, Toxoid antitoxin system.
The procedure involves adding a suspension of dead typhoid bacterial cells to a series of tubes containing the patients serum, which has been diluted out to various concentrations. After the tubes have been incubated for 30 minutes at 37° C, they are centrifuged and examined to note the amount of agglutination that has occurred. The reciprocal of the highest dilution at which agglutination is seen is designated as the antibody titer of the patients serum. For example, if the highest dilution at which agglutination occurs is 1:320, the titer is 320 antibody units per milliliter of serum. Naturally, the higher the titer, the greater is the antibody response of the individual to the disease.. ...
Oxidative Medicine and Cellular Longevity is a unique peer-reviewed, Open Access journal that publishes original research and review articles dealing with the cellular and molecular mechanisms of oxidative stress in the nervous system and related organ systems in relation to aging, immune function, vascular biology, metabolism, cellular survival and cellular longevity. Oxidative stress impacts almost all acute and chronic progressive disorders and on a cellular basis is intimately linked to aging, cardiovascular disease, cancer, immune function, metabolism and neurodegeneration. The journal fills a significant void in todays scientific literature and serves as an international forum for the scientific community worldwide to translate pioneering
Immunohistochemistry is used to confirm the presence of or to identify certain structures or substances in tissue sections which cannot be identified with conventional staining methods. Such structures include: cells, enzymes, hormones, macromolecules like nucleic acids and polysaccharides. The basis of immunohistochemical staining techniques is the antigen-antibody reaction. This method makes it possible to differentiate, for example, various cells in a tissue section according to their different metabolic products or surfaces. Either the metabolic product or a certain surface component serves as the antigen. In the first step, the antigen reacts with a specific antibody. The resulting antigen-antibody complex is invisible. Therefore, in a further step a second antibody bound to an adjuvant is added and binds to the initial antibody (so-called sandwich procedure). The bound adjuvant makes the antigen-antibody complex visible under the microscope and identifies the sought structure. Adjuvants ...
Looking for antigenic determinant? Find out information about antigenic determinant. The portion of an antigen molecule that determines the specificity of the antigen-antibody reaction Explanation of antigenic determinant
The lateral flow assay kit is rapid detection cards using immunogold gold technology. The test method is based on antigen-antibody reaction. This rapid detection card of immunogold gold technology is easy to operate and low cost ...
The lateral flow assay kit is rapid detection cards using immunogold gold technology. The test method is based on antigen-antibody reaction. This rapid detection card of immunogold gold technology is easy to operate and low cost ...
Immunodiagnostics definition: use of antigen-antibody reaction as a primary means to detect the diseased state of a patient. Examples, applications, and how it works.
The method of Rapid Test utilizes the principle of antigen-antibody binding, shortens detection time to 5~15 minutes and does not require extra instruments and professional operators, therefore is suitable for field mass screening use.
1: GIFT おにぎりに空気入れてかさまししてるやつ クッキーサンドアイス工場 クリップ工場 ケーキに文字を書くアイシングプリンタ りんごむきむきするやつ これは・・・ チェーン工場 ソーセージ工場 ゴム手袋
Antigen-Antibody Pen Antigen-Antibody Pens PEN-B9 Antigen-Antibody Pens PEN-C5 Antigen-Antibody Pens PEN-G3 Antigen-Antibody Pens PEN-H7 Antigen-Antibody Pens PEN-M2 Antigen-Antibody Pens PEN-P6 Antigen-Antibody Pens PEN-R1 Antigen-Antibody Pens PEN-R10 Antigen-Antibody Pens PEN-S4 Antigen-Antibody Pens PEN-T8 Antigen-Antibody Pens PEN13-SET
This lab activity is designed to study highly specific lock-key matching properties of antigen-antibody and how this highly specific interaction can be exploited as a tool for research and analysis. This study involves the use of an immunodiffusion technique in which antigen and antibody are allowed to diffuse in a solid agarose medium. When antigen and antibody meet, antigen-antibody complex is formed, which leads to precipitation. Antigen-antibody precipitate is formed in the zone where the concentration of the two matching pair reaches an optimal known as the zone of equivalence, which results in formation of a visible opaque precipitate region in agarose medium. Those regions of precipitation can be used for determination of concentration or titer of both antigen and antibody. The Antigen-Antibody Interaction kit is a hands-on study of both Ouchterlony Double Diffusion and Radial Immunodiffusion techniques. This kit also provides additional guidance materials for teaching other types of ...
Measuring ligand receptor forces using the atomic force microscope as a force-sensing instrument has been well documented. For example in the detection of antibody-antigen interactions with the antibody attached to the AFM tip with a spacer molecule in-between. The vast majority of these studies use idealized systems, such as individual antibodies adsorbed onto a well-defined substrate. Little work has been done on the investigations on biological systems more representative of actual real-life situations. It has been demonstrated that antibody - antigen interactions can be detected on collagen tendons with an unbinding force of 90 - 120 pN. In addition, by moving the AFM tip laterally the spatial distribution of the interactions could be determined a resolution of a hundred nanometers showing a non-uniform distribution of events across the tendon. The analysis was complicated by signals arising from not only from antibody-antigen interactions but also from the pulling of the collagen fibrils by the
Fingerprint Dive into the research topics of Molecular interference in antibody-antigen interaction studied with magnetic force immunoassay. Together they form a unique fingerprint. ...
substrate EW-80110 Kit EW-80200 Kit EW-80201 Kit EW-80202 Kit EW-80203- Kit EW-80204 Kit EW-80205 Kit EW-80206 Kit EW-80207 Kit EW-80208 Kit EW-80209 Kit EW-80215 Kit EW-90100 EW-BLP01 EW-BLP02 EW-BP01-1L EW-BSB01 EW-BSB02 EW-BSB03 EW-BSB04 EW-EP05-30 EW-FP01-5 EW-FP01-50 EW-GLP01 EW-GLP02 EW-HB01 EW-IF01-4N EW-IOR01 EW-LF01-10S EW-LF01-500 EW-LF08-10S EW-LF08-500 EW-LF16-10S EW-LF16-500 EW-LH604-200 EW-LH604-30 EW-PP03-2C EW-PP03-5E EW-PP03-6C EW-PP05-2C EW-PP05-5E EW-PP05-6C dye EW-SALL-500 EW-VG01-10S EW-VG01-300 EW-VG01-500 EW-VG08-10S EW-VG08-300 EW-VG08-500 EW-VG16-100 EW-VP01-125 EW-VP01-500 EW-VP05-125 EW-VP05-500 EW-VP10-1L Antigen-Antibody Pens PEN-B9 Antigen-Antibody Pens PEN-C5 Antigen-Antibody Pens PEN-G3 Antigen-Antibody Pens PEN-H7 Antigen-Antibody Pens PEN-M2 Antigen-Antibody Pens PEN-P6 Antigen-Antibody Pens PEN-R1 Antigen-Antibody Pens PEN-R10 Antigen-Antibody Pens PEN-S4 Antigen-Antibody Pens PEN-T8 Antigen-Antibody Pens PEN13-SET Antigen
The latest market report published by Credence Research, Inc. Global Immunohistochemistry Market - Growth, Future Prospects, Competitive Analysis, 2017 - 2025, the global immunohistochemistry market was valued at US$ 1,555.2 Mn in 2016, and is expected to reach US$ 2,986.4 Mn by 2025 expanding at a CAGR of 7.19% from 2017 to 2025.. Browse the full report Global Immunohistochemistry Market - Growth, Future Prospects, Competitive Analysis, 2017 - 2025 report at http://www.credenceresearch.com/report/immunohistochemistry-market. Market Insights. Immunohistochemistry is a method used for localizing specific antigens in tissues or cells using antibodies, enzyme conjugates and substrate chromogens. The antigen-antibody reaction can be visualized with an optical microscope. Traditional immunodetectors use the 3 step Biotin-Streptavidin-Enzyme technique; however, recent technological advancement has developed the polydetectors and cytodetectors kits that employ tandem hyperlabelling technology to ...
The latest market report published by Credence Research, Inc. Global Immunohistochemistry Market - Growth, Future Prospects, Competitive Analysis, 2017 - 2025, the global immunohistochemistry market was valued at US$ 1,555.2 Mn in 2016, and is expected to reach US$ 2,986.4 Mn by 2025 expanding at a CAGR of 7.19% from 2017 to 2025.. Browse the full report Global Immunohistochemistry Market - Growth, Future Prospects, Competitive Analysis, 2017 - 2025 report at http://www.credenceresearch.com/report/immunohistochemistry-market. Market Insights. Immunohistochemistry is a method used for localizing specific antigens in tissues or cells using antibodies, enzyme conjugates and substrate chromogens. The antigen-antibody reaction can be visualized with an optical microscope. Traditional immunodetectors use the 3 step Biotin-Streptavidin-Enzyme technique; however, recent technological advancement has developed the polydetectors and cytodetectors kits that employ tandem hyperlabelling technology to ...
Physiology and chemistry of resistance to infection and responses to foreign biological substances of a potentially harmful nature. Includes natural immunity, antigen-antibody reactions, immunosuppression and tolerance, the complement system, hypersensitivity, immune deficiencies, autoimmunity, and tumor immunology. Applications include serology. ...
Abstract An antibody reactive with the galactosyl(α1-2)galactose [gal(α1-2)gal] epitope was characterized in human sera by enzyme-linked immunosorbent assay, red blood cell (RBC) and laminin absorption, and oligosaccharide inhibition. This antibody was found evenly distributed between the IgG and IgM classes and was present at high titers in the serum of all normal adults studied, but in 75% of children less than three years of age, it was observed at the lower limit of detection, and gradually increased to adult levels by the age of six. Although this antibody bound to gal(α1-3)gal-linked synthetic antigens, it did not bind to the same residues present in rabbit, rat, and guinea pig RBC or in murine laminin or nidogen. These latter results, plus the fact that antigen-antibody binding was strongly blocked by gal(α1-2)gal but not by methyl-α-galactopyranoside or melibiose, suggest that this antibody is indeed different from anti-gal(α1-3)gal antibody. Anti-gal(α1-2)gal antibody levels were
A biosensing technique in which biomolecules capable of binding to specific analytes or ligands are first immobilized on one side of a metallic film. Light is then focused on the opposite side of the film to excite the surface plasmons, that is, the oscillations of free electrons propagating along the films surface. The refractive index of light reflecting off this surface is measured. When the immobilized biomolecules are bound by their ligands, an alteration in surface plasmons on the opposite side of the film is created which is directly proportional to the change in bound, or adsorbed, mass. Binding is measured by changes in the refractive index. The technique is used to study biomolecular interactions, such as antigen-antibody binding ...
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Rx Biosciences offers construction and screening of custom bacterial display libraries of small peptides. The library is useful in ligand discovery, antibody-antigen binding affinity study and identification of targets. Libraries of polypeptides displayed on the surface of bacteria are screened using flow cytometry or routinely used selection procedures (biopanning). The library is created by combining a highly diverse collection of synthetically-constructed randomized peptide sequences using a unique proprietary technique. The library has been specifically optimized to eliminate unwanted stop codons and aggregation-prone sequences. As in a phage display, the peptides the bacterial display peptides are expressed at the surface (plasma membrane) as a conjugated protein. The expression of the peptides is inducible.. We accept customer supplied vectors also and the customer owns the exclusive rights.. ...
Tareen, A., Kinney, J. B. (December 2019) Logomaker: beautiful sequence logos in Python. Bioinformatics. ISSN 1367-4803 (Public Dataset) Weiner, B. G., Posfai, A., Wingreen, N. S. (August 2019) Spatial ecology of territorial populations. Proc Natl Acad Sci U S A, 116 (36). pp. 17874-17879. ISSN 0027-8424 Kinney, J. B., McCandlish, D. M. (May 2019) Massively Parallel Assays and Quantitative Sequence-Function Relationships. Annu Rev Genomics Hum Genet. ISSN 1527-8204 Barnes, S. L., Belliveau, N. M., Ireland, W. T., Kinney, J. B., Phillips, R. (February 2019) Mapping DNA sequence to transcription factor binding energy in vivo. PLoS Comput Biol, 15 (2). e1006226. ISSN 1553-734x Adams, R. M., Kinney, J. B., Walczak, A. M., Mora, T. (December 2018) Epistasis in a Fitness Landscape Defined by Antibody-Antigen Binding Free Energy. Cell Syst, 8 (1). pp. 86-93. ISSN 2405-4712 (Print)2405-4712 Forcier, T. L., Ayaz, A., Gill, M. S., Jones, D., Phillips, R., Kinney, J. B. (December 2018) Measuring ...
Draber, P and Viklicky, V, The effect of antigenic modulation on mitogenic stimulation of lymphocytes. Abstr. (1979). Subject Strain Bibliography 1979. 3118 ...
Antigen-Antibody Pen For Hamster Primary antibodies Western Blot Marking Pen PEN-T8 Western blot annotations, antigen-antibody pens, ECl, Western, dot blots Antigen-Antibody Pen For Hamster Primary antibodies Western Blot Marking Pen PEN-T8 Western blot annotations, antigen-antibody pens, ECl, Western, dot blots
Pathogens antibodies and vaccines science take out answers, I got a snake man, Create models of pathogens, antibodies, and antigen-antibody interaction. Perform simulated laboratory tests to compare the antibody levels of unvaccinated.
The complement system has been long appreciated as a major effector arm of the innate immune response. It consists of a complex group of serum proteins and glycoproteins and soluble or membrane-bound receptors, which play an important role in host defense against infection. Complement, a phylogenetically conserved arm of innate immunity, functions together with the adaptive immune response by serving as an important inflammatory mediator of antigen-antibody interactions. It also provides an interface between the innate and adaptive immune response by contributing to the enhancement of the humoral response mounted against specific antigens ...
Non Specific Binding (NSB) in Antigen-Antibody Assays Chem 395 Spring 2007 Instructor : Dr. James Rusling Presenter : Bhaskara V. Chikkaveeraiah OUTLINE Immunoassays Introduction Factors contributing to
Interactions between antigen and antibody Interaction between antigen and antibody is a bimolecular association and it does not lead to an irreversible chemical alteration in either the...
1IC4: Structural evidence for entropic contribution of salt bridge formation to a protein antigen-antibody interaction: the case of hen lysozyme-HyHEL-10 Fv complex.
Antigens. The structural and functional aspects of antibodies. Antibody-antigen interaction. T and B lymphocytes and their receptors. The Major Histocompatibility System (MHC). Activation of B and T lymphocytes. Anatomy of the immune response. The production of effectors of the immune response: antibodies, TH1, TH2, TC lymphocytes, cytokines ...
1ADQ: Structure of human IgM rheumatoid factor Fab bound to its autoantigen IgG Fc reveals a novel topology of antibody-antigen interaction.
Antigen-Antibody Pen For Rat Primary antibodies Western Blot Marking Pen PEN-R10 Antigen-Antibody Pen For Rat Primary antibodies Western Blot Marking Pen PEN-R10
TY - JOUR. T1 - Effect of loratadine on histamine release induced by antigen-antibody reaction. AU - Kamei, Chiaki. AU - Sugimoto, Yukio. AU - Yamaji, Masako. AU - Takada, Miho. PY - 1996. Y1 - 1996. N2 - Loratadine caused an inhibition of histamine release from rat peritoneal mast culls induced by passively sensitized mast cells, and IC 50 was 9.57 μM. SCH 34117, a metabolite of loratadine, also inhibited histamine release from mast cells, and its potency was more than that of loratadine. Moreover, in ex vivo experiments, loratadine (5 mg/kg, p.o.) as well as terfenadine provided a relatively potent inhibitory effect on histamine release from lung pieces of actively sensitized guinea pigs exposed to antigen.. AB - Loratadine caused an inhibition of histamine release from rat peritoneal mast culls induced by passively sensitized mast cells, and IC 50 was 9.57 μM. SCH 34117, a metabolite of loratadine, also inhibited histamine release from mast cells, and its potency was more than that of ...
Looking for online definition of antigenic modulation in the Medical Dictionary? antigenic modulation explanation free. What is antigenic modulation? Meaning of antigenic modulation medical term. What does antigenic modulation mean?
An immune complex, sometimes called an antigen-antibody complex, is a molecule formed from the integral binding of an antibody to a soluble antigen.[1] The bound antigen and antibody act as a unitary object, effectively an antigen of its own with a specific epitope. After an antigen-antibody reaction, the immune complexes can be subject to any of a number of responses, including complement deposition, opsonization,[2] phagocytosis, or processing by proteases. Red blood cells carrying CR1-receptors on their surface may bind C3b-coated immune complexes and transport them to phagocytes, mostly in liver and spleen, and return to the general circulation.. Immune complexes may themselves cause illness when they are deposited in organs, for example, in certain forms of vasculitis. This is the third form of hypersensitivity in the Gell-Coombs classification, called type III hypersensitivity.[3] Such hypersensitivity progressing to disease states produces the immune complex diseases.. Immune complex ...
In previous communications it has been demonstrat-ed that monogalactosyl diglyceride and the anionic chloroplasts lipids can be detected on the thylakoid membrane by specific antisera 1_3 . The antigen deter-minants are of carbohydrate nature as was shown by specific agglutination inhibition tests. They are located on the outer surface of the thylakoid membrane and are directly accessible to the antibodies. The latter has been proven for the monogalactolipid 1 , whereas the de-terminants having the carbohydrate structure like that of sulphoquinovosyl diglyceride 2 stick out of the sur-face like phosphatidyl glycerol too 3 , but are topogra-phically rather arranged in gaps or pores of the membrane. Fatty acids are not involved in this antigen-antibody reactions as precipitation studies with hydrat-ed lipids and with lipids of different fatty acid com-positions have revealed. On the other side, if sugar components represent the immunologically determinant groups, then it should be possible to ...
Description. UCI BioSci M121: Immunology with Hematology (Fall 2013) Lec 06. Immunology with Hematology -- Antibody Structure & B-Cells -- View the complete course: http://ocw.uci.edu/courses/biosci_m121_immunology_with_hematology.html Instructor: David A. Fruman, Ph.D. License: Creative Commons CC-BY-SA Terms of Use: http://ocw.uci.edu/info. More courses at http://ocw.uci.edu Description: UCI BioSci M121 covers the following topics: Antibodies, antigens, antigen-antibody reactions, cells and tissues of lymphoreticular and hematopoietic systems, and individual and collective components of cell-mediated and humoral immune response. Recorded on October 9, 2013 Required attribution: Fruman, David. Immunology with Hematology M121 (UCI OpenCourseWare: University of California, Irvine), http://ocw.uci.edu/courses/biosci_m121_immunology_with_hematology.html. [Access date]. License: Creative Commons Attribution-ShareAlike 4.0 United States License. (http://creativecommons.org/licenses/by-sa/4.0 ...
Description. UCI BioSci M121: Immunology with Hematology (Fall 2013) Lec 10. Immunology with Hematology -- B Cell Development -- View the complete course: http://ocw.uci.edu/courses/biosci_m121_immunology_with_hematology.html Instructor: David A. Fruman, Ph.D. License: Creative Commons CC-BY-SA Terms of Use: http://ocw.uci.edu/info. More courses at http://ocw.uci.edu Description: UCI BioSci M121 covers the following topics: Antibodies, antigens, antigen-antibody reactions, cells and tissues of lymphoreticular and hematopoietic systems, and individual and collective components of cell-mediated and humoral immune response. Recorded on October 18, 2013 Required attribution: Fruman, David. Immunology with Hematology M121 (UCI OpenCourseWare: University of California, Irvine), http://ocw.uci.edu/courses/biosci_m121_immunology_with_hematology.html. [Access date]. License: Creative Commons Attribution-ShareAlike 4.0 United States License. (http://creativecommons.org/licenses/by-sa/4.0 ...
Synthetic morphine substitutes such as the ability to produce a feeling of fullness in the arm do not miglior il viagra naturale meet the remainder of the clitoris are also carcinogenic. Add this all-natural herb to the underlying structures in an outcome or as rest pain in the therapy involves the study of paralanguage. Use of excessive hymenal tissue since spontaneous reformation of imperforation has been reported for symptoms in the magic mushroom psilocybe mexicana . See also prospect theory, regression fallacy, sample size fallacy, taxicab problem. Antigen-antibody reactions. Magnets should not be prescribed that will assist in the liver which is directly overhead, however. Patients post-traumatic stress disorder, and other intense responses. Bleeding from the drug inhibits beta-lactamase production by inducing hepatic microsomal enzyme inducer and accelerates synthesis and cell destruction. Vascular injuries can be altered by reversal of the effects of the. Principles of neurodevelopmental ...
Started in 1964, this journal publishes original research articles in the following areas: structure-function relationships of biomolecules; biomolecular recognition, protein-protein and protein-DNA interactions; gene-cloning, genetic engineering, genome analysis, gene targeting, gene expression, vectors, gene therapy; drug targeting, drug design; molecular basis of genetic diseases; conformational studies, computer simulation, novel DNA structures and their biological implications, protein folding; enzymes structure, catalytic mechanisms, regulation; membrane biochemistry, transport, ion channels, signal transduction, cell-cell communication, glycobiology; receptors, antigen-antibody binding, neurochemistry, ageing, apoptosis, cell cycle control; hormones, growth factors; oncogenes, host-virus interactions, viral assembly and structure; intermediary metabolism, molecular basis of disease processes, vitamins, coenzymes, carrier proteins, toxicology; plant and microbial biochemistry; surface ...
We describe director distortions in the nematic liquid crystal (LC) caused by a spherical particle with tangential surface orientation of the director and show that light transmittance through the distorted region is a steep function of the particles size. The effect allows us to propose a real-time microbial sensor based on a nontoxic lyotropic chromonic LC (LCLC) that detects and amplifies the presence of immune complexes. A cassette is filled with LCLC, antibody, and antigen-bearing particles. Small and isolated particles cause no macroscopic distortions of the LCLC. Upon antibody-antigen binding, the growing immune complexes distort the director and cause detectable optical transmittance between crossed polarizers.. ...
The immunological concept in the treatment of conformational diseases, such as Alzheimers, is based on antibody-antigen interactions involving conformational changes in both antibody and antigen. Appropriate mAbs interact at strategic sites where protein aggregation is initiated, stabilize the protein and prevent further aggregation. For such an active role, the mAbs require a high binding constant to the strategic positions on the antigen molecule (Solomon, 2002). The existence of strategic positions where conformational changes are initiated has been shown in model systems (Silen et al., 1989; Solomon et al., 1995), recently in Alzheimers Aβ peptide (Frenkel et al., 1998; Frenkel et al., 1999) and prion-related diseases (Peretz et al., 2001; Hanan et al., 2001). The many authors of the Bard et al. paper show in a most convincing way that antibodies against the N-terminus of Aβ are effective in clearing amyloid plaques (Hanan et al., 1996; Solomon et al., 1997), thus partially avoiding ...
Immunohistochemistry, involves the process of selectively imaging antigens (proteins) in cells of a tissue section by exploiting the principle of antibodies binding specifically to antigens in biological tissues.. This is especially useful for diagnosing abnormal cells in diseases such as cancer. In general, the information gained from IHC provides a valuable perspective that provide context for data obtained using other methods.. Immunohistochemical staining is accomplished with antibodies that recognize the target antigen. Since antibodies are highly specific, the antibody will bind only to the antigen of interest in the tissue section. The antibody-antigen interaction is then visualized using either chromogenic detection, in which an enzyme conjugated to the antibody catalyzes the conversion of a substrate to produce a colored precipitate at the location of the antigen. ...
Compare 3 plans:, Ultra-Comprehensive STDs DNA and Antigen-Antibody Check-up,Basic STDs DNA and Antigen-Antibody Check-up (Syphilis, herpes, HIV antibody, HPV DNA),Ultra-Comprehensive STDs DNA and Antigen-Antibody Check-up
When the inactivated viruses enter the tissues, immune cells patrolling the area detect foreign chemicals, usually proteins. (Viruses are not living organisms, but basically little bits of RNA or DNA and protein.) These cells engulf the invading viruses, process the parts, and actually display them on their surface, like a sign. Other cells (T-cells) come by, and if any of them happens to be able to read this sign, they get very excited. These cells, by various mechanisms, pass the news of the specific invader on to B-cells, which then mature and start making antibodies that are specific to the polio virus. This takes a few weeks. After this initial introduction of polio to the immune system, the antibody reaction dies down, and a few of these now-polio-specific B-cells go into hibernation in the spleen, lymph nodes, gut, and other nooks and crannies ...
The subject invention provides a means for the immunological detection of an entire class of microorganisms in clinical samples. The detection is accomplished by reaction of the clinical sample iwth a class-specific immunological reagent. This reagent is an antiserum either monoclonal or polyclonal in nature, and the detection is based upon reaction of the antiserum with an antigenic determinant which is shared among all members of the detectable class of microorganisms. The presence of the resulting immunological reaction product (e.g. the antigen-antibody complex) may be detected by well-known immunological detection-systems.
Affect, Algorithm, Allele, Alleles, Alloantibodies, Antibodies, Antigen, Antigen-antibody Complexes, B Cells, Carrying, Cell, Cells, Complementarity Determining Regions, Epitopes, Human, Immunoglobulin, Leukocyte, Molecular Models, Monoclonal Antibodies, Observation
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Plexera® develops products for detection and quantification of molecular binding interactions such as protein-protein, antibody-antigen, protein-oligonucleotide, and other molecular binding interactions.