MIB-1 Labeling Index is Very Important Proliferative Factor for Lymphangioma

Our concept for the treatment of lymphangioma is simple resection if it is small and adjacent to the surface of the skin and intralesional injection of OK- 32 if it is big. Resection of the mass is performed if its size has reduced after observation, but persisted. The rapid growth of the lymphangioma has been considered to be due to inflammation and invasion of the vessels, but their relationship remains unclear. Our hypothesis is that the Mib1-labeling index of endothelial cells of fast-growing lymphangioma is larger than that of non-proliferating lymphangioma. Mib-1 labeling index shows their ability of proliferation. In our study, we could show the high potential cells of lymphangioma had high MIB1 index using the immunological technique of the pathology.

Preparation of artificial antibodies and development of an antibody-based indirect ELISA for the detection of ancient wool

An immunological technique was proposed for the detection of ancient wool.

Predators of the Alfalfa Aphids Acyrthosiphon pisum (Harris), Aphis craccivora Koch, and Therioaphis trifolii (Monell) (Hemiptera: Aphidoidea) as Determined by the Serological Technique

Predators of the Alfalfa Aphids Acyrthosiphon pisum (Harris), Aphis craccivora Koch,and Therioaphis trifolii (Monell) (Hemiptera: Aphidoidea) as Determined by the Serological TechniqueAbstract. The serology is an immunological technique based on antigen/antibody reactions in where its main advantages are high sensitivity and specificity that allows the biological recognition at the molecular level. This study evaluates the use of serology technique to determine the predators of the alfalfa aphids Acyrthosiphon pisum (Harris), Aphis craccivora Koch,and Therioaphis trifolii (Monell)(Hemiptera: Aphidoidea). The aphid samplings to obtain the antibodies and their possible predators to be used as antigens were carried out in the alfalfa fields of the Embrapa Pecuária Sudeste Unit, São Carlos, SP. In the period from August 2011 to July 2012. A total of 2,161 arthropod predators, including insects and spiders, were tested. The antibodies obtained for the aphid A. craccivora, A. pisum, and T. trifolii showed partial identity nevertheless still allowed to recognize the predators of alfalfa aphids. Among the insects, syrphids and chrysopids presented the highest percentage of positive results in the serological tests. The species A. craccivora was the most preyed aphid.Determinação de Predadores dos Pulgões da Alfafa Acyrthosiphon pisum (Harris), Aphis craccivora Koch e Therioaphis trifolii (Monell)(Hemiptera: Aphidoidea) por meio da Técnica SerológicaResumo. A serologia é uma técnica imunológica baseada em reações antígeno/anticorpo, em que suas principais vantagens são a alta sensibilidade e especificidade que permitem o reconhecimento biológico em nível molecular. Este trabalho avalia o uso da técnica serológica para determinar os predadores dos pulgões da alfafa, Acyrthosiphon pisum (Harris), Aphis craccivora Koch e Therioaphis trifolii (Monell) (Hemiptera: Aphidoidea). As coletas dos pulgões para a obtenção dos anticorpos e de seus possíveis predadores para serem utilizados como antígenos foram realizadas nos campos de alfafa da Unidade da Embrapa Pecuária Sudeste, São Carlos, SP. no período de agosto de 2011 a julho de 2012. Foram testados 2.161 artrópodes predadores, incluindo insetos e aranhas. Os anticorpos obtidos para os pulgões A. craccivora, A. pisum, e T. trifolii mostraram identidade parcial mas, ainda assim, permitiu reconhecer os predadores dos pulgões da alfafa. Dentre os insetos, sirfídeos e crisopídeos foram os que apresentaram as maiores porcentagens de resultados positivos nos testes serológicos. A. craccivora foi o afídeo mais consumido pelos predadores.

Assessment of an ELISA Laboratory Exercise

The enzyme-linked immunosorbent assay (ELISA) is a powerful immunological technique for quantifying small amounts of compounds and has been used in research and clinical settings for years. Although there are laboratory exercises developed to introduce the ELISA technique to students, their ability to promote student learning has not been thoroughly assessed. We found that a commercially available ELISA kit increased student performance on pre- and post-tests in three undergraduate college courses, especially in those taught to general-education students. Student confidence levels about ELISA methodology, as well as comfort level in performing the technique, increased significantly in both general- education and biology-major courses.

Determination of Antibodies (IgG, IgM) against Toxoplasma gondii in Some Iraqi individuals by using ELISA technique

A total of 258 voluntary blood donors (males 101; females 157) in the age range of 18-52 yr among males and 18-55 yr among females were examined for Toxoplasma gondii antibodies (IgG), and (IgM) by immunological technique (Enzyme linked Immunosorbant Assay) during the period from March 2009 to April 2010. This study covered a wide range of factors including immunological, age ,sex , place of residence and symptoms that may have a possible relationship with toxoplasmosis. Results presented in this study showed clearly that 38 (14.7%) of individuals participated in this study having IgG Toxoplasma Ab, among those 10 samples (9.9%) were males and 28 samples (17.8%) were females. Moreover, we found the prevalence of IgM seropositivity in the study population to be 5.8% ,as well as, the prevalence of IgM was 1.98 % in males and 8.3% in females. In addition to , the results of current study indicated that the seroprevalence of IgG Toxoplasma antibodies are more than IgM antibodies ,besides , the peak period range of toxoplasma gondii antibodies IgG among males donors was 30 to 39 years, while among female donors, the highest detection of Toxoplasma gondii antibodies IgG was between the ages of 40 to 49. What's more, the peak age range of Toxoplasma gondii antibodies IgM among males and females donors was 19 to 29 years. In conclusion , Our study showed a high prevalence of T. gondii antibodies in healthy voluntary blood donors. It may be appropriate to include screening test (ELISA) for T. gondii also in the pre transfusion blood testing schedule.

Anovel Immunological Technique for Identification of Human Seminal Fluid

An immunological technique was investigated for the detection of human semen in forensic analysis.This technique included a preparation of anti-human seminal plasma antibodies, by immunizing rabbits with treated human semen. The human semen was treated with an acid to prevent cross reactivity with other human body fluids. The antibody produced was tested against different animal,s seminal fluid samples (dog, goat ,sheep, cow) and human body fluids( saliva, blood , vaginal fluid, ear wax and human semen). It was found that using this developed technique was only selectively responsed with human semen . The prepered kit was evaluated and tested in Forensic laboratory- Ministry of Health. Finally, results were obtained in a comparison with the recommended techniques.

Effect of Enrichment Medium on Real-Time Detection of Salmonella enterica from Lettuce and Tomato Enrichment Cultures

Three enrichment broths commonly used for detection of Salmonella (buffered peptone water [BPW], tryptic soy broth [TSB], and universal preenrichment broth [UPB]) were compared for use in real-time SYBR Green PCR detection of Salmonella introduced into enrichment cultures made from store-bought lettuce and tomatoes. The produce served as a source of normal plant microbiota to measure how well DNA-based detection methods for Salmonella work in a suspension of plant-associated bacteria that may be closely related to Salmonella. A qualitative assessment of the background microbiota that grew in the three enrichment broths cultures from tomato and lettuce samples revealed that different bacteria predominated in the different broths. Results obtained with five produce-related outbreak Salmonella strains and PCR primers directed toward three different Salmonella genes suggest that the ability to detect Salmonella from these enrichment cultures by real-time PCR was 10 to 1,000 times better with TSB enrichment cultures. Detection levels were similar between the different enrichment media when an immunomagnetic separation method was used; however, the immunological technique did not enhance detection from TSB enrichment cultures. Detection could be affected by the medium and by the background microbiota. An immunomagnetic separation method may be useful in BPW and UPB enrichment cultures but not in TSB enrichment cultures.