Diagnostic performance of two specific Schistosoma japonicum immunological tests for screening Schistosoma haematobium in school children in Zambia.
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Diagnostic performance of two specific Schistosoma japonicum immunological tests for screening Schistosoma haematobium in school children in Zambia.
Dipstick Dye Immunoassay (DDIA) and directly Haemagglutination Assay (IHA), two kits are commercially available that has been widely used for the screening of Schistosoma japonicum in the People’s Republic of China. Whether they can be used for screening of Schistosoma haematobium unclear. In order to evaluate the diagnostic efficiency DDIA and IHA for screening Schistosoma haematobium, serum samples were collected from students in endemic areas in Zambia, South Africa, and tested by DDIA and IHA with a single-blind manner. Meanwhile, the students are microscopically examined by Schistosoma infection and soil-transmitted worms, visually observed for parasite eggs.
Of the 148 students enrolled, 61% tested positive for S. haematobium infection, while 31% and 36% of students were infected with hookworm and Ascaris respectively. Regarding the parasitological tests as reference standards, for the diagnosis of S. haematobium infection, IHA carried higher sensitivity (74%, 95% CI: 65% -83%) compared DDIA (60%, 95% CI: 49% – 70%) , DDIA IHA sensitivity and significantly higher in students aged 10-14 years compared to 7-9 years old group. The specificity DDIA and IHA is 61% (95% CI: 49% -74%) and 72% (95% CI: 60% -84%), respectively. Co-infection with decreased specificity STHs DDIA but has no impact on that IHA. Our study shows that IHA has more potential as an alternative diagnostic tool to identify schistosomiasis haematobium but needs further improvement.
paraneoplastic neurological syndromes (PNS) and autoimmune encephalitis (AE) is a rare neurological disorder, which has similar symptoms, but vary in results and treatment strategies. In a retrospective statistical study we evaluate the results of the test serum and CSF autoantibodies from patients suspected PNS 2362 and 1034 patients with suspected AE. For testing of autoantibodies, immunoblot assay (PNS) and cell-based indirect immunofluorescence assay (AE) used. Autoantibodies present in 8% of patients with suspected PNS: anti-Yo> anti-Hu> anti-MA2> anti-CV2> anti-titin> anti-Zic4> anti-amphiphysin> anti-Ri> anti-GAD65> anti Sox1> anti-recoverin.
Most of the older women who are affected. Autoantibodies present in 5.8% of patients with suspected AE: anti-NMDAR (young women)> anti-LGI1 (middle-aged men)> anti-GABABR (elderly man)> anti-Caspr2 (men). our results are in accordance with the data described in the literature. The number of patients suspected civil servants and AE showed an upward trend, in which the testing of autoantibodies with modern laboratory diagnostic methods to help in the early introduction of appropriate therapy.
Diagnostic performance of two specific Schistosoma japonicum immunological tests for screening Schistosoma haematobium in school children in Zambia.
[Morphology and immunological variation of Borrelia burgdorferi and diagnostic methods].
diagnostic problems observed in patients infected with Borrelia burgdorferi is a significant barrier for therapeutic decision making. It seems that the pathogen is characterized by morphological and immunological variation in a certain stage of development.
Bacteria have the ability to morphological changes into the cell wall of a shortage of spheroplast, L-shape, bleb-like spirochetes, and cysts body / round shape. It also has the ability to create a biofilm, which is the main barrier to the antibiotic.
Description: MM-102 is an antagonist of MLL1 with IC50 value of 2.4nM [1].Mixed lineage leukemia 1 (MLL1) is a histone H3 lysine 4 (H3K4) methyltransferase.
Description: MM-102 is an antagonist of MLL1 with IC50 value of 2.4nM [1].Mixed lineage leukemia 1 (MLL1) is a histone H3 lysine 4 (H3K4) methyltransferase.
Description: MM-102 is an antagonist of MLL1 with IC50 value of 2.4nM [1].Mixed lineage leukemia 1 (MLL1) is a histone H3 lysine 4 (H3K4) methyltransferase.
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of T180
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of T180
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of T180
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IF, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of Y182
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IF, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of Y182
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IF, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of Y182
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of T180/Y182
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of T180/Y182
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of T180/Y182
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of Y323
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of Y323
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat. This p38 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human p38 around the non-phosphorylation site of Y323
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat, Chicken. This p38 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human p38
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat, Chicken. This p38 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human p38
Description: A polyclonal antibody for detection of p38 from Human, Mouse, Rat, Chicken. This p38 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human p38
Description: p38 is a protein encoded by the MAPK14 gene which is approximately 41,2 kDa. p38 is localised to the cytoplasm and nucleus. It is involved in activated TLR4 signalling, the IL-2 pathway, toll-like receptor signalling pathways, the VEGF signalling pathway and 4-1BB pathway. This protein falls under the MAP kinase family. It acts as an integration point for multiple biochemical signals, and is involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is activated by various environmental stresses and proinflammatory cytokines. p38 is expressed in the brain, heart, placenta, pancreas and skeletal muscle. Mutations in the MAPK14 gene may result in patellar tendinitis and lumbosacral lipoma. STJ94878 was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. This polyclonal antibody detects endogenous levels of p38 protein.
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human SAP 102 . This antibody is tested and proven to work in the following applications:
Description: HG-10-102-01 is a potent and selective inhibitor of leucine-rich repeat kinase 2 (LRRK2) with the IC50 values of 20.3nM and 3.2nM for wild type LRRK2 and LRRK2 [G1019S], respectively [1].
Description: HG-10-102-01 is a potent and selective inhibitor of leucine-rich repeat kinase 2 (LRRK2) with the IC50 values of 20.3nM and 3.2nM for wild type LRRK2 and LRRK2 [G1019S], respectively [1].
Description: HG-10-102-01 is a potent and selective inhibitor of leucine-rich repeat kinase 2 (LRRK2) with the IC50 values of 20.3nM and 3.2nM for wild type LRRK2 and LRRK2 [G1019S], respectively [1].
Description: HG-10-102-01 is a potent and selective inhibitor of leucine-rich repeat kinase 2 (LRRK2) with the IC50 values of 20.3nM and 3.2nM for wild type LRRK2 and LRRK2 [G1019S], respectively [1].
Description: HG-10-102-01 is a potent and selective inhibitor of leucine-rich repeat kinase 2 (LRRK2) with the IC50 values of 20.3nM and 3.2nM for wild type LRRK2 and LRRK2 [G1019S], respectively [1].
Bacteria are characterized by significant heterogeneity and polymorphism of the antigen, which greatly inhibited detailed definition of pathogens, since antibodies produced may differ significantly from the accepted patterns and also cause cross reactions. The above conditions affecting the reliability of diagnostic tests, particularly screening, which can lead to incorrect treatment decisions.
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