Immunoelectrophoresis
A technique that combines protein electrophoresis and double immunodiffusion. In this procedure proteins are first separated by gel electrophoresis (usually agarose), then made visible by immunodiffusion of specific antibodies. A distinct elliptical precipitin arc results for each protein detectable by the antisera.
Immunoelectrophoresis, Two-Dimensional
Counterimmunoelectrophoresis
Immunodiffusion
Immune Sera
Coccidioidin
Cross Reactions
Electrophoresis, Polyacrylamide Gel
Blood Proteins
Rabbits
Immunochemistry
Electrophoresis, Agar Gel
Chemical Precipitation
Chromatography, Gel
Isoelectric Focusing
Electrophoresis, Cellulose Acetate
Carbohydrates
Immunosorbent Techniques
Antigen-Antibody Complex
Antigen-Antibody Reactions
Paraproteinemias
gamma-Globulins
Serum globulins that migrate to the gamma region (most positively charged) upon ELECTROPHORESIS. At one time, gamma-globulins came to be used as a synonym for immunoglobulins since most immunoglobulins are gamma globulins and conversely most gamma globulins are immunoglobulins. But since some immunoglobulins exhibit an alpha or beta electrophoretic mobility, that usage is in decline.
Electrophoresis
Trichloroacetic Acid
Hemagglutination Tests
Agglutination Tests
Danazol
A synthetic steroid with antigonadotropic and anti-estrogenic activities that acts as an anterior pituitary suppressant by inhibiting the pituitary output of gonadotropins. It possesses some androgenic properties. Danazol has been used in the treatment of endometriosis and some benign breast disorders.
Beta-Globulins
Immunologic Techniques
Ultracentrifugation
Acholeplasma laidlawii
Amino Acids
Electrophoresis, Disc
Electrophoresis in which discontinuities in both the voltage and pH gradients are introduced by using buffers of different composition and pH in the different parts of the gel column. The term 'disc' was originally used as an abbreviation for 'discontinuous' referring to the buffers employed, and does not have anything to do with the shape of the separated zones.
Precipitin Tests
Serum Globulins
Isoelectric Point
Immunoglobulin G
Paraproteins
Abnormal immunoglobulins synthesized by atypical cells of the MONONUCLEAR PHAGOCYTE SYSTEM. Paraproteins containing only light chains lead to Bence Jones paraproteinemia, while the presence of only atypical heavy chains leads to heavy chain disease. Most of the paraproteins show themselves as an M-component (monoclonal gammopathy) in electrophoresis. Diclonal and polyclonal paraproteins are much less frequently encountered.
Dysentery, Amebic
Glycoproteins
Species Specificity
The restriction of a characteristic behavior, anatomical structure or physical system, such as immune response; metabolic response, or gene or gene variant to the members of one species. It refers to that property which differentiates one species from another but it is also used for phylogenetic levels higher or lower than the species.
Bence Jones Protein
Complement Fixation Tests
Serologic tests based on inactivation of complement by the antigen-antibody complex (stage 1). Binding of free complement can be visualized by addition of a second antigen-antibody system such as red cells and appropriate red cell antibody (hemolysin) requiring complement for its completion (stage 2). Failure of the red cells to lyse indicates that a specific antigen-antibody reaction has taken place in stage 1. If red cells lyse, free complement is present indicating no antigen-antibody reaction occurred in stage 1.
Actinomyces
Hypergammaglobulinemia
Chromatography
Techniques used to separate mixtures of substances based on differences in the relative affinities of the substances for mobile and stationary phases. A mobile phase (fluid or gas) passes through a column containing a stationary phase of porous solid or liquid coated on a solid support. Usage is both analytical for small amounts and preparative for bulk amounts.
Chromatography, Ion Exchange
Immunoglobulin kappa-Chains
Chromatography, Affinity
Immunoglobulin lambda-Chains
Meningitis
Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6)
Stanozolol
Antigens, Surface
Antithrombin III Deficiency
Immunoglobulin A
Chemistry
Antibody Specificity
Chemical Phenomena
Serum Albumin
Detergents
Complement C3
A glycoprotein that is central in both the classical and the alternative pathway of COMPLEMENT ACTIVATION. C3 can be cleaved into COMPLEMENT C3A and COMPLEMENT C3B, spontaneously at low level or by C3 CONVERTASE at high level. The smaller fragment C3a is an ANAPHYLATOXIN and mediator of local inflammatory process. The larger fragment C3b binds with C3 convertase to form C5 convertase.
Blood Platelets
Fluorescent Antibody Technique
Test for tissue antigen using either a direct method, by conjugation of antibody with fluorescent dye (FLUORESCENT ANTIBODY TECHNIQUE, DIRECT) or an indirect method, by formation of antigen-antibody complex which is then labeled with fluorescein-conjugated anti-immunoglobulin antibody (FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT). The tissue is then examined by fluorescence microscopy.
Complement C4
Immunoglobulins
Multi-subunit proteins which function in IMMUNITY. They are produced by B LYMPHOCYTES from the IMMUNOGLOBULIN GENES. They are comprised of two heavy (IMMUNOGLOBULIN HEAVY CHAINS) and two light chains (IMMUNOGLOBULIN LIGHT CHAINS) with additional ancillary polypeptide chains depending on their isoforms. The variety of isoforms include monomeric or polymeric forms, and transmembrane forms (B-CELL ANTIGEN RECEPTORS) or secreted forms (ANTIBODIES). They are divided by the amino acid sequence of their heavy chains into five classes (IMMUNOGLOBULIN A; IMMUNOGLOBULIN D; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M) and various subclasses.
Immunoassay
alpha 1-Antitrypsin
Serotyping
Cell Membrane
alpha-Macroglobulins
Glycoproteins with a molecular weight of approximately 620,000 to 680,000. Precipitation by electrophoresis is in the alpha region. They include alpha 1-macroglobulins and alpha 2-macroglobulins. These proteins exhibit trypsin-, chymotrypsin-, thrombin-, and plasmin-binding activity and function as hormonal transporters.
Immunoglobulin Light Chains
Chromatography, DEAE-Cellulose
Rhamnose
Antibodies
Streptococcus
Antithrombin III
Transferrin
Radioimmunoassay
Classic quantitative assay for detection of antigen-antibody reactions using a radioactively labeled substance (radioligand) either directly or indirectly to measure the binding of the unlabeled substance to a specific antibody or other receptor system. Non-immunogenic substances (e.g., haptens) can be measured if coupled to larger carrier proteins (e.g., bovine gamma-globulin or human serum albumin) capable of inducing antibody formation.
Alpha-Globulins
Platelet Membrane Glycoproteins
Cell Wall
Absorption
Latex Fixation Tests
Trypsin
Agar
A complex sulfated polymer of galactose units, extracted from Gelidium cartilagineum, Gracilaria confervoides, and related red algae. It is used as a gel in the preparation of solid culture media for microorganisms, as a bulk laxative, in making emulsions, and as a supporting medium for immunodiffusion and immunoelectrophoresis.
Blood Coagulation Factors
Hemagglutination
Immunoglobulin M
von Willebrand Factor
A high-molecular-weight plasma protein, produced by endothelial cells and megakaryocytes, that is part of the factor VIII/von Willebrand factor complex. The von Willebrand factor has receptors for collagen, platelets, and ristocetin activity as well as the immunologically distinct antigenic determinants. It functions in adhesion of platelets to collagen and hemostatic plug formation. The prolonged bleeding time in VON WILLEBRAND DISEASES is due to the deficiency of this factor.
Macromolecular Substances
Peptide Hydrolases
Enzyme-Linked Immunosorbent Assay
An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed.
Membrane Proteins
Fibrinogen
Plasma glycoprotein clotted by thrombin, composed of a dimer of three non-identical pairs of polypeptide chains (alpha, beta, gamma) held together by disulfide bonds. Fibrinogen clotting is a sol-gel change involving complex molecular arrangements: whereas fibrinogen is cleaved by thrombin to form polypeptides A and B, the proteolytic action of other enzymes yields different fibrinogen degradation products.
Polyethylene Glycols
Polymers of ETHYLENE OXIDE and water, and their ethers. They vary in consistency from liquid to solid depending on the molecular weight indicated by a number following the name. They are used as SURFACTANTS, dispersing agents, solvents, ointment and suppository bases, vehicles, and tablet excipients. Some specific groups are NONOXYNOLS, OCTOXYNOLS, and POLOXAMERS.
von Willebrand Diseases
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Solubility
Escherichia coli
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
Multiple Myeloma
A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY.
Factor VIII
Blood-coagulation factor VIII. Antihemophilic factor that is part of the factor VIII/von Willebrand factor complex. Factor VIII is produced in the liver and acts in the intrinsic pathway of blood coagulation. It serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin.
Liver
Sodium Dodecyl Sulfate
Teichoic Acids
Mycobacterium
Streptococcus mutans
Goats
Microscopy, Electron
Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen.
Lipoproteins, HDL
A class of lipoproteins of small size (4-13 nm) and dense (greater than 1.063 g/ml) particles. HDL lipoproteins, synthesized in the liver without a lipid core, accumulate cholesterol esters from peripheral tissues and transport them to the liver for re-utilization or elimination from the body (the reverse cholesterol transport). Their major protein component is APOLIPOPROTEIN A-I. HDL also shuttle APOLIPOPROTEINS C and APOLIPOPROTEINS E to and from triglyceride-rich lipoproteins during their catabolism. HDL plasma level has been inversely correlated with the risk of cardiovascular diseases.
Complement System Proteins
Serum glycoproteins participating in the host defense mechanism of COMPLEMENT ACTIVATION that creates the COMPLEMENT MEMBRANE ATTACK COMPLEX. Included are glycoproteins in the various pathways of complement activation (CLASSICAL COMPLEMENT PATHWAY; ALTERNATIVE COMPLEMENT PATHWAY; and LECTIN COMPLEMENT PATHWAY).
Homogeneous pyruvate kinase isolated from yeast by two different methods is indistinguishable from pyruvate kinase in cell-free extract. (1/2055)
In this report, we have compared homogeneous yeast (Saccharomyces cerevisiae) pyruvate kinase to enzyme from cell-free extracts in several different ways: 1) isoelectric focusing of cell-free extracts indicates one peak of pyruvate kinase activity whose isoelectric point is the same as that of the pure enzyme; 2) antibody prepared to the pure enzyme produces a single, fused precipitin line against enzyme in the cell-free extract and pure enzyme; 3) immunoelectrophoresis of cell-free extract produces one precipitin arc which has the same mobility as that of the pure enzyme; and 4) immunoprecipitation of the pure enzyme from cell-free extract with subsequent solubilization in 1% sodium dodecyl sulfate and electrophoresis on sodium dodecyl sulfate-polyacrylamide gels produces a single protein band attributable to pyruvate kinase which co-migrates with the purified enzyme. Within the limits of the sensitivity of the methods employed, we conclude that the homogeneous pyruvate kinase prepared from yeast lysed either by Manton-Gaulin homogenization (Aust, A., Yun, S.-L., and Suelter, C. (1975) Methods Enzymol. 42, 176-182) or by toluolysis (Yun, S.-L., Aust, A.E., and Suelter, C.H. (1977) J. Biol. Chem. 251, 124-128) is identical with pyruvate kinase in cell-free extract. (+info)Enzymatic and immunological characterization of the Mycobacterium fortuitum complex. (2/2055)
The arylsulfatase isozymes of Mycobacterium fortuitum, M. peregrinum, M. chelonei subsp. chelonei, and M. chelonei subsp. abscessus were examined to determine the isozymal and immunological relationship among the members of the M. fortuitum complex. Cell extracts were subjected to electrophoresis on agarose and polyacrylamide gel, and arylsulfatase activity was localized using beta-naphthyl sulfate as substrate. Unique zymograms were produced for M. fortuitum, M. peregrinum, and M. chelonei which were characteristic for each species. The immunological relationship among the sulfatases was assayed by using immunodiffusion and immunoelectrophoresis followed by sulfatase staining for the enzyme. One of the isozymes of M. fortuitum and M. peregrinum cross-reacted, showing immunological identity. Antisera to sulfatases of M. fortuitum and M. peregrinum did not react with sulfatases of M. chelonei. The characterization of sulfatase isozymes in extracts of organisms in the M. fortuitum complex suggests the division of the M. fortuitum complex into two species, M. fortuitum and M. chelonei, with subspecies designations. (+info)The phenoloxidases of the ascomycete Podospora anserina. Structural differences between laccases of high and low molecular weight. (3/2055)
In order to investigate the extent of the relationship between the three copper-containing glycoproteins, laccases I, II and III (Mr70000, 80000 and 390000 respectively) of Podospora anserina, the following experiments were carried out on laccases II and III: (a) determination of amino acid composition; (b) determination of N-terminal and C-terminal amino acid; (c) determination of sugar composition; (d) dissociation studies on native and denatured laccases and also after removal of copper from the enzymes; (e) digestion of the carbohydrate moieties with the aid of glycosylhydrolases. A comparison between the results of these experiments and data previously obtained with laccase I allows the following conclusions to be drawn. 1. Laccases II and III are not identical. 2. Neither of these low molecular weight laccases are as complete molecules subunits of the oligomeric laccase I. 3. The possibility of partial identity of amino acid sequences of laccases I and III can not be excluded. 4. Laccase II possibly consists of subunits of Mr37000 whereas laccase III does not. 5. Digestion of 50% of the carbohydrate content leads to complete loss of serological specificity (serological reaction and cross reaction). This finding is discussed with regard to the possible role of the carbohydrate moiety as antigenic determinants and thus as the reason for the immunological relationship. As a consequence, at least three independent structural genes for laccases must be assumed. (+info)Inhibition of human seminal fluid DNA polymerase by an IgG fraction of seminal plasma from vasectomized men. (4/2055)
Immunoglobulin G (IgG) was isolated from ejaculates of intact and vasectomized men by precipitation with ammonium sulphate and DEAE-cellulose ionexchange chromatography. Velocity centrifugation revealed that all of the IgG from intact males was 7S protein while less than 40% of the seminal IgG of vasectomized men cosedimented with the 7S marker; the remaining, immunologically unidentifiable, protein was considerably smaller and heterogeneous in size. Only the 7S IgG from the post-vasectomy ejaculates inhibited the activity of a DNA polymerase from the seminal fluid of an intact male. These results suggest that formation of antibody reactive with the seminal fluid DNA polymerase is one manifestation of a vasectomy-associated autoimmune response in man. (+info)Complement activity in middle ear effusions. (5/2055)
Evidence for complement utilization in middle ear fluids (MEF) from patients with otitis media with effusion was sought. It was found that cleavage products of C3, C4 and Factor B could be demonstrated immunochemically in MEF, and that native C3 was present in much lower concentrations than other proteins, relative to their serum concentrations. Haemolytic assays for C1-C5 showed that early complement components are inactivated in MEF. Potential mechanisms for complement utilization in MEF are discussed. (+info)Enterobacterial common antigen: isolation from Shigella sonnei, purification and immunochemical characterization. (6/2055)
In the studies presented the effective procedure of isolation and purification of enterobacterial common antigen from Shigella sonnei has been elaborated. The method is based on sonification of bacterial suspension in the presence of lysozyme and EDTA and subsequent extraction of the pellet with boiling water. The crude extract of common antigen was purified by fractionation with ethanol and chromatography on silica gel and Sephadex LH-20. The comparison of several extraction procedures of enterobacterial common antigen from Shigella sonnei proved that the method described above is most effective. The purified enterobacterial common antigen preparation obtained preserved full biological activity: antigenicity (precipitation and activity in enzyme-linked immunosorbent assay), immunogenicity in rabbits, ability to coat erythrocytes (passive hemagglutination) and inhibitory activity in passive hemagglutination. The pure enterobacterial common antigen was identified to 90% as a polymer of N-acetyl-D-mannosaminuronic acid and N-acetyl-D-glucosamine (2:1, molar ratio), O-acetylated and containing 3.2% fatty acids (C16:0 and C18:1, not oleic). It contains 5.3% nitrogen, less than 4% protein, less than 0.5% phosphorus and less than 1.6% neutral sugar; glycerol and RNA were not found in the preparation. (+info)Immune response in the garter snake (Thamnophis ordinoides). (7/2055)
Garter snakes (Thamnophis ordinoides) were immunized with hen egg albumin, human gamma-globulin and Keyhole limpet haemocyanin in Freund's adjuvant. Antibody was consistently detected by radioimmunoelectrophoresis and in three different gamma- and beta-globulin precipitin lines called IgM (approximately or equal to 20S), Ig-1 (approximately or equal to 9S) and Ig-2 (approximately or equal to 8-5S). Early antibody (day 31 after immunization) was frequently Ig-M whereas Ig-2 and especially Ig-1 were detectable for the longest duration (992 days). After immunization with antigen in Freund's adjuvant, Ig-1 serum concentration showed the greatest increase, from almost undetectable levels to the most prominent immunoglobulin in immune serum. (+info)Plant microbody proteins. Purification and glycoprotein nature of glyoxysomal isocitrate lyase from cucumber cotyledons. (8/2055)
1. Isocitrate lyase from cotyledons of cucumber seedlings (Cucumis sativus) has been purified 100-fold. Two methods of preparing the soluble glyoxylate cycle enzyme are described: an elaborated method which used crude extracts of cucumber cotyledons, and another procedure which started with purified glyoxysomes from 4-day-old cotyledons and included a separation of glyoxysomal matrix enzymes by zonal centrifugation. The product behaved as a single species when tested by (a) polyacrylamide gel electrophoresis in the presence of dodecyl sulfate, (b) zonal centrifugation, and (c) double immunodiffusion against rabbit antibody to isocitrate lyase. 2. Isocitrate lyase of cucumber glyoxysomes exhibited a molecular weight of 255,000 and was composed of four apparently identical subunits of Mr 64,000. An isoelectric point of 5.9 was determined. 3. It was shown that isocitrate lyase is a glycoprotein, (a) by Schiff stain on polyacrylamide gels, (b) by periodate oxidation of the enzyme, subsequent reduction with NaB[3H]4 and electrophoretic analysis of the labelled glycoprotein, and (c) by incorporation of [3H]glucosamine in vivo into a protein which could be precipitated with antibodies to isocitrate lyase and revealed a 64,000-Mr band upon electrophoresis. (+info)Rocket immunoelectrophoresis experiment principles, materials and operating procedures
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Immunoelectrophoresis
Crossed immunoelectrophoresis is also called two-dimensional quantitative immunoelectrophoresis ad modum Clarke and Freeman or ... Rocket immunoelectrophoresis is one-dimensional quantitative immunoelectrophoresis. The method has been used for quantitation ... Identification of nanomaterial interaction with C3 protein complement and 2D immunoelectrophoresis 2D immunoelectrophoresis is ... As a result, newer immunoelectrophoresis techniques have largely supplanted the conventional immunoelectrophoresis. Homburger, ...
Counterimmunoelectrophoresis
Electrophoresis Immunoelectrophoresis Ling IT.; Cooksley S.; Bates PA.; Hempelmann E.; Wilson RJM. (1986). "Antibodies to the ... "Counter immunoelectrophoresis". Sherris, John C.; Ryan, Kenneth J.; Ray, C. L. (2004). Sherris medical microbiology: an ...
Affinity electrophoresis
Immunoelectrophoresis Aizpurua-Olaizola, Oier; Sastre Torano, Javier; Pukin, Aliaksei; Fu, Ou; Boons, Geert Jan; de Jong, ... "rocket immunoelectrophoresis", affinity electrophoresis may be used as an alternative quantification of the protein. Some of ...
Immunofixation
Immunoelectrophoresis Miller, Linda E. (2021). "18, Immunoproliferative Diseases: Role of the Laboratory in Evaluating ... Immunofixation as immunoelectrophoresis, takes place in two steps: The first step is identical for both techniques. It consists ...
Pierre Grabar
Simple and inexpensive, immunoelectrophoresis quickly became a widely-used method of analysis in clinical biology with ... His award-winning development of Immunoelectrophoresis made it possible to identify specific bodily proteins, opening new ... In 1953 Grabar developed immunoelectrophoresis, combining electrophoresis and immunochemical analysis to create an "immuno- ... Arquembourg, Pierre C. (1975). Immunoelectrophoresis: Theory, Methods, Identifications, Interpretation. S. Karger. pp. 6, 12. ...
Pavle Trpinac
Trpinac, P., Bugarski, O .: Immunoelectrophoresis. Archives of Pharmacy 1959; 5: 257. Pavlović, V., Trpinac, P .: Application ...
Apolipoprotein D
Ayrault Jarrier M, Levy G, Polonovski J (August 1963). "[Study of Human Serum Alpha-Lipoproteins by Immunoelectrophoresis]". ...
Major urinary proteins
Roy AK, Neuhaus OW (March 1966). "Identification of rat urinary proteins by zone and immunoelectrophoresis". Proceedings of the ...
Antigen-antibody interaction
Sophisticated applications include ELISA, enzyme-linked immunospot (Elispot), immunofluorescence, and immunoelectrophoresis. ... "Identification of Cytosolic Antigens from GW-39 Adenocarcinoma Cells by Crossed Immunoelectrophoresis and Immunofluorescence". ...
Barbital
Solutions of sodium barbital have also been used as pH buffers for biological research, e.g., in immunoelectrophoresis or in ... Monthony JF, Wallace EG, Allen DM (October 1978). "A non-barbital buffer for immunoelectrophoresis and zone electrophoresis in ...
Armed Forces Institute of Pathology (Pakistan)
The technology of immunoelectrophoresis, immunoprecipitation in gel and fluorescent microscopy was introduced. In his days a ...
Immunochemistry
... immunoelectrophoresis, immunophenotyping, immunochromatographic assay and cyflometry. One of the earliest examples of ...
Tree nut allergy
Goetz, DW (July 2005). "Cross-reactivity among edible nuts: double immunodiffusion, crossed immunoelectrophoresis, and human ... crossed immunoelectrophoresis, and human specific IgE serologic surveys". Annals of Allergy, Asthma & Immunology. 95 (1): 45-52 ...
Gerald Penn (immunologist)
Gerald Penn is a clinical immunologist, and a pioneer in the field of clinical immunoelectrophoresis. He was a student of Henry ...
Hypoallergenic dog breed
"Characterization of extract of dog hair and dandruff from six different dog breeds by quantitative immunoelectrophoresis. ...
Gel electrophoresis of proteins
... or as immunoelectrophoresis.[citation needed] Traditionally, two classes of blood proteins are considered: serum albumin and ... or gel electrophoresis Immunoelectrophoresis Immunofixation SDD-AGE Native gel electrophoresis QPNC-PAGE Paraprotein Fast ... immunoelectrophoresis, counterelectrophoresis, and capillary electrophoresis. Each method has many variations with individual ...
Auchterlonie
Ouchterlony O (1970), Handbook of Immunodiffusion and Immunoelectrophoresis, Ann Arbor, MI: Ann Arbor-Humphrey Science ...
Academy of Natural Sciences of Drexel University
Allozymes, DNA-DNA hybridization, immunoelectrophoresis, restriction site analyses of mitochondrial DNA and serology were used ...
Örjan Ouchterlony
Ouchterlony O (1970), Handbook of Immunodiffusion and Immunoelectrophoresis, Ann Arbor, MI: Ann Arbor-Humphrey Science ...
Barbiturate
Sodium barbital and barbital have also been used as pH buffers for biological research, e.g., in immuno-electrophoresis or in ...
Waldenström macroglobulinemia
Immunoelectrophoresis and immunofixation studies help identify the type of immunoglobulin, the clonality of the light chain, ...
Agarose gel electrophoresis
Gel electrophoresis Immunodiffusion, Immunoelectrophoresis SDD-AGE Northern blot SDS-polyacrylamide gel electrophoresis ...
Agarose
... is also used widely for a number of other applications, for example immunodiffusion and immunoelectrophoresis, as the ...
Cryoglobulinemia
The precipitated cryoglobulins are examined by immunoelectrophoresis and immunofixation to detect and quantify the presence of ...
Antibody
... immunoelectrophoresis, and magnetic immunoassay. Antibodies raised against human chorionic gonadotropin are used in over the ...
Methods to investigate protein-protein interactions
Pull-down assays are a common variation of immunoprecipitation and immunoelectrophoresis and are used identically, although ...
Electrophoresis
Dielectrophoresis Electroblotting Gel electrophoresis Gel electrophoresis of nucleic acids Immunoelectrophoresis Isoelectric ...
IEP
... may refer to: Immunoelectrophoresis Inclusion-exclusion principle Integrated electric propulsion Isoelectric point ...
List of MeSH codes (H01)
... two-dimensional immunoelectrophoresis MeSH H01.181.529.307.437.575 - iontophoresis MeSH H01.181.529.307.437.663 - isoelectric ... immunoelectrophoresis MeSH H01.181.529.307.437.568.250 - counterimmunoelectrophoresis MeSH H01.181.529.307.437.568.520 - ...
Electrophoresis (disambiguation)
... commonly used to analyse proteins Immunoelectrophoresis, used to separate and characterize biomolecules on basis their ...
Immunoelectrophoresis - blood: MedlinePlus Medical Encyclopedia
Diagnosis of cystic echinococcosis: ultrasound imaging or countercurrent immunoelectrophoresis?
... View/. Open. emhj_2001_7_6_907 ... Countercurrent immunoelectrophoresis could detect only 62.0% of cases, whereas the pathology and ultrasound results were ... The results of countercurrent immunoelectrophoresis were compared with pathology and ultrasound reports to determine whether ... ultrasound imaging or countercurrent immunoelectrophoresis?. EMHJ - Eastern Mediterranean Health Journal, 7 (6), 907-911, ...
Browsing by Subject "Immunoelectrophoresis"
LOINC 49274-4 - Immunoelectrophoresis for Serum or Plasma Narrative
LOINC Code 49274-4 Immunoelectrophoresis for Serum or Plasma Narrative ... 49274-4Immunoelectrophoresis for Serum or Plasma NarrativeActive. Fully-Specified Name. Component. Interpretation. Property. ... Immunoelectrophoresis. Additional Names. Short Name. Interpretation SerPl IEP-Imp. Display Name. Interpretation IEP Nar [Interp ...
Light Chain-Associated Renal Disorders Workup: Laboratory Studies, Imaging Studies, Procedures
IMSEAR at SEARO: Detection of Bacteroides infection by counter immunoelectrophoresis test.
Analyses of genetic variants of l-glycerol-3-phosphate dehydrogenase in Drosophila melanogaster by two-dimensional gel...
keywords = "immunoelectrophoresis, two-dimensional electrophoresis, α-GPD null mutants",. author = "Lee, {Chi Yu} and David ... Mutants which express no apparent α-GPDH activity were analyzed by two-dimensional gels and immunoelectrophoresis in an attempt ... Mutants which express no apparent α-GPDH activity were analyzed by two-dimensional gels and immunoelectrophoresis in an attempt ... Mutants which express no apparent α-GPDH activity were analyzed by two-dimensional gels and immunoelectrophoresis in an attempt ...
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Immunoelectrophoresis, Immunohistochemistry, Immunocytochemistry, Antibody Identification, Western Blotting), End Users ( ... 5.2.3. Immunoelectrophoresis. 5.2.4. Immunohistochemistry. 5.2.5. Immunocytochemistry. 5.2.6. Antibody Identification. 5.2.7. ... Immunoelectrophoresis. - Immunohistochemistry. - Immunocytochemistry. - Antibody Identification. - Western Blotting. Global ... Immunoelectrophoresis, Immunohistochemistry, Immunocytochemistry, Antibody Identification, Western Blotting), End Users ( ...
Publication Year: 2019 / Source: 2019 v.48 no.2 / Subject: Avibacterium paragallinarum and chickens / Subject term: bacterial...
Volume 36, Issue 3 | Microbiology Society
Antigenic Homogeneity among Legionella pneumophila Serogroups 1 to 6 Evaluated by Crossed Immunoelectrophoresis JETTE M. ... In addition, reproducibility of the antigenic profile of L. pneumophila by crossed immunoelectrophoresis was demonstrated. ... pneumophila serogroup 1 system and the polyvalent crossed immunoelectrophoresis system with L. pneumophila serogroups 1 to 6 ...
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Plus it
Goat F(ab')2 Anti Mouse (IgG+IgM+IgA) secondary antibody preadsorbed TRI
ELISASerumElectrophoresisRocket immunoelectrophoresisCountercurrent immunoelectrophoresisAssayProteinsDiagnosisTestElectrophoresisImmunoprecipitationPrecipitinCountercurrentUrine immunoelectrophoresisImmunodiffusionCross-reactivityMonospecificSerum and urineHuman serumChromatographyMonoclonal gammopathyAntibody reactsAntiseraSpecificityMethodsCounter
ELISA6
- RÉSUMÉ L'objectif de cette étude réalisée en Iraq était de définir la sensibilité et la spécificité d'un test ELISA commercial pour la détection de l'antigène de Giardia lamblia dans les selles. (who.int)
- Frequencies of autoantibodies to Sm, nRNP, Ro (SSA) and La (SSB) were determined by countercurrent immunoelectrophoresis (CIE) and/or enzyme linked immunosorbent assays (ELISA) in 106 whites and 60 blacks with systemic lupus erythematosus. (nih.gov)
- Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule rat IgG. (jacksonimmuno.com)
- Most workers reacted positively with Micropolyspora-faeni antigen, but is was not possible with either ELISA or counter immunoelectrophoresis to separate the ill from the workers who were not ill. (cdc.gov)
- Specificity By immunoelectrophoresis and ELISA, this antibody reacts specifically with human IgE. (qedbio.com)
- 1975). An antigen detection ELISA and counter-immunoelectrophoresis have been used to detect infections of Brugia pahangi in cats (Au et al. (aavp.org)
Serum5
- Serum immunoelectrophoresis is a lab test that measures proteins called immunoglobulins in the blood. (medlineplus.gov)
- Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Goat Serum. (abcam.com)
- Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Mouse IgA alpha and anti-Mouse serum. (novusbio.com)
- Based on Immunoelectrophoresis, no reactivity is observed to: non-immunoglobulin rabbit serum proteins, serum proteins from bovine, human, or mouse , IgG from human or mouse. (thermofisher.com)
- Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Peroxidase, anti- Rat IgG, anti-Rat IgG F(ab')2 and anti-Rat Serum. (rockland.com)
Electrophoresis2
- Lee, CY, Niesel, D & Bewley, GC 1980, ' Analyses of genetic variants of l-glycerol-3-phosphate dehydrogenase in Drosophila melanogaster by two-dimensional gel electrophoresis and immunoelectrophoresis ', Biochemical Genetics , vol. 18, no. 9-10, pp. 1003-1018. (utmb.edu)
- Methods for detection of Bence Jone proteins include conventional high-resolution electrophoresis or capillary zone electrophoresis followed by confirmation through immunofixation electrophoresis (preferable) or immunoelectrophoresis. (richardvigilantebooks.com)
Rocket immunoelectrophoresis2
- The proteins of 46 human bile specimens, collected by several different routes have been studied by crossed immunoelectrophoresis, by rocket immunoelectrophoresis and by radioimmunoassay. (bmj.com)
- Rocket Immunoelectrophoresis (RIEP) also known as electro-immuno diffusion is a simple, quick and reproducible method for determining the concentration of antigen (Ag) in an unknown sample. (microbiologynote.com)
Countercurrent immunoelectrophoresis3
- Diagnosis of cystic echinococcosis: ultrasound imaging or countercurrent immunoelectrophoresis? (who.int)
- The results of countercurrent immunoelectrophoresis were compared with pathology and ultrasound reports to determine whether serological tests could be helpful for diagnosis. (who.int)
- Countercurrent immunoelectrophoresis could detect only 62.0% of cases, whereas the pathology and ultrasound results were positive for 96.3% of cases. (who.int)
Assay1
- including immunofluorescent assay, enzyme immunoassay, counter-immunoelectrophoresis and radio-immune precipitation assay. (who.int)
Proteins5
- Light-chain proteins are best detected and identified using immunoelectrophoresis with monospecific antikappa and antilambda sera. (medscape.com)
- Mutants which express no apparent α-GPDH activity were analyzed by two-dimensional gels and immunoelectrophoresis in an attempt to identify and characterize the inactive proteins. (utmb.edu)
- The next step is to use immunoelectrophoresis to determine the exact type of proteins in the blood. (healthline.com)
- Quantitative immunoelectrophoresis of proteins in human erythrocyte membranes. (semanticscholar.org)
- In the past, specific proteins were analyzed using a variety of specialized methods, such as radial immunodiffusion, immunoelectrophoresis or using dedicated nephelometers. (roche.com)
Diagnosis1
- The most valuable serologic test in the diagnosis of human hydatid disease is immunoelectrophoresis. (medscape.com)
Test1
- IMSEAR at SEARO: Detection of Bacteroides infection by counter immunoelectrophoresis test. (who.int)
Electrophoresis5
- The purified enzyme was free of other known brush border enzymes and appeared homogeneous in immunoelectrophoresis and polyacrylamide gel electrophoresis in the presence of SDS. (nih.gov)
- Electrophoresis and immunoelectrophoresis of concentrated urine. (brighamandwomens.org)
- Immunoelectrophoresis (IEP) was the first practical method that combined electrophoresis and immunoprecipitation for identifying and characterizing proteins within complex mixtures. (biofron.com)
- Comparisons of the migration patterns of various protein fractions in gels by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, line-rocket immunoelectrophoresis, and enzyme-specific staining confirmed the identity of the two strains of R . quintana and their similarity to the vole agent. (microbiologyresearch.org)
- The isolated protein was homogenous by the criteria of polyacrylamide gel electrophoresis, gel filtration chromatography, immuno-double diffusion and immunoelectrophoresis. (ias.ac.in)
Immunoprecipitation2
- Anti-Apolipoprotein B, goat polyclonal, recognizes human apolipoprotein B. It is validated for Western blotting, immunoelectrophoresis, and immunoprecipitation. (merckmillipore.com)
- Immunoelectrophoresis in which immunoprecipitation occurs when antigen at the cathode is caused to migrate in an electric field through a suitable medium of diffusion against a stream of antibody migrating from the anode as a result of endosmotic flow. (lookformedical.com)
Precipitin3
- Streptococcus group B typing: comparison of counter-immunoelectrophoresis with the precipitin method. (nih.gov)
- The different elapid venoms, with the exception of that of N. naja oxiana , showed a considerable number of identical and similar precipitin components by immunodiffusion and immunoelectrophoresis. (ajtmh.org)
- In immunoelectrophoresis and radial immunodiffusion (Ouchterlony), using various antiserum concentrations against fresh normal swine plasma a single precipitin line is obtained which shows a reaction of identity with the precipitin line obtained with purified alpha-1antitrypsin. (lsbio.com)
Countercurrent2
Urine immunoelectrophoresis2
- Urine immunoelectrophoresis revealed kappa light chains. (hindawi.com)
- Immunofixation is similar to urine immunoelectrophoresis , but it may give more rapid results. (healthing.ca)
Immunodiffusion1
- In precipitating techniques as immunoelectrophoresis and single or double radial immunodiffusion to identify the presence of alpha-1antitrypsin in swine plasma or other body fluids or to determine its concentration. (lsbio.com)
Cross-reactivity2
- Weak serological cross-reactivity was observed by haemagglutination and two-dimensional immunoelectrophoresis. (microbiologyresearch.org)
- Minimum cross-reactivity is observed to the light chains or to non-immunoglobulin goat serum proteins based on immunoelectrophoresis. (agrisera.com)
Monospecific2
- Light-chain proteins are best detected and identified using immunoelectrophoresis with monospecific antikappa and antilambda sera. (medscape.com)
- Monospecific as determined by immunoelectrophoresis (IEP) against 2X pooled human serum and neat pooled human plasma. (merckmillipore.com)
Serum and urine3
- Protein immunoelectrophoresis of serum and urine from the proband and from 19 family members was performed to detect monoclonal immunoproteins. (nih.gov)
- Within this family, a sibship of seven included three individuals (including the proband) with histologically verified MM and two individuals with a monoclonal gammopathy of unknown significance (MGUS), as determined by immunoelectrophoresis of serum and urine. (nih.gov)
- A finding of increased rouleaux formation suggests multiple myeloma, and the workup should be directed toward immunoelectrophoresis of serum and urine. (medscape.com)
Human serum2
- Antisera forms multiple arcs against normal human serum by immunoelectrophoresis. (leebio.com)
- The affinity purified anti human haptoglobin forms a single preciptin band with human serum haptoglobin and purified human haptoglobin by immunoelectrophoresis and double diffusion. (leebio.com)
Chromatography1
- Summary: The partial characterization of a mouse hydrosoluble testis specific protein by crossed immunoelectrophoresis, ion‐exchange chromatography and SDS‐Page was made. (uchile.cl)
Monoclonal gammopathy1
- Serum immunoelectrophoresis showed IgM K-type monoclonal gammopathy. (biomedcentral.com)
Antibody reacts1
- This antibody reacts with the heavy chains on goat IgG based on immunoelectrophoresis. (agrisera.com)
Antisera1
- In crossed immunoelectrophoresis the polymer reacted with specific antisera to serotypes. (microbiologyresearch.org)
Specificity1
- Specificity of hyper immune sera raised against CPS was tested by counter current immunoelectrophoresis. (ijcea.org)
Methods1
- A manual of quantitative immunoelectrophoresis: methods and applications. (microbiologyresearch.org)
Counter1
- The development of a Klebsiella serotyping method by counter-current immunoelectrophoresis (CIE) is described. (nih.gov)