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1.
Annu Rev Biomed Eng ; 23: 433-459, 2021 07 13.
Artigo em Inglês | MEDLINE | ID: mdl-33872519

RESUMO

Since aptamers were first reported in the early 2000s, research on their use for the detection of health-relevant analytical targets has exploded. This review article provides a brief overview of the most recent developments in the field of aptamer-based biosensors for global health applications. The review provides a description of general aptasensing principles and follows up with examples of recent reports of diagnostics-related applications. These applications include detection of proteins and small molecules, circulating cancer cells, whole-cell pathogens, extracellular vesicles, and tissue diagnostics. The review also discusses the main challenges that this growing technology faces in the quest of bringing these new devices from the laboratory to the market.


Assuntos
Aptâmeros de Nucleotídeos , Técnicas Biossensoriais , Saúde Global , Proteínas
2.
Gene Expr Patterns ; 20(2): 99-105, 2016 03.
Artigo em Inglês | MEDLINE | ID: mdl-26820751

RESUMO

Homeobox (Hox) genes are involved in body plan of embryo along the anterior-posterior axis. Presence of several Hox genes in white adipose tissue (WAT) and brown adipose tissue (BAT) is indicative of involvement of Hox genes in adipogenesis. We propose that differentiation inducing agents viz. isobutyl-methyl-xanthine (IBMX), indomethacin, dexamethasone (DEX), triiodothyronine (T3) and insulin may regulate differentiation in brown adipose tissue through Hox genes. In vitro culture of brown fat stromalvascular fraction (SVF) in presence or absence of differentiation inducing agents was used for establishing relationship between fat accumulation in differentiated adipocytes and expression of Hox genes. Relative expression of Pref1, UCP1 and Hox genes was determined in different stages of adipogenesis. Presence or absence of IBMX, indomethacin and DEX during differentiation of proliferated pre-adipocytes resulted in marked differences in expression of Hox genes and lipid accumulation. In presence of these inducing agents, lipid accumulation as well as expression of HoxA1, HoxA5, HoxC4 &HoxC8 markedly enhanced. Irrespective of presence or absence of T3, insulin down regulates HoxA10. T3 results in over expression of HoxA5, HoxC4 and HoxC8 genes, whereas insulin up regulates expression of only HoxC8. Findings suggest that accumulation of fat in differentiated adipocytes is linked with expression of Hox genes.


Assuntos
Adipócitos Marrons/metabolismo , Tecido Adiposo/crescimento & desenvolvimento , Proteínas de Homeodomínio/biossíntese , Fosfoproteínas/biossíntese , Fatores de Transcrição/biossíntese , 1-Metil-3-Isobutilxantina/administração & dosagem , Adipócitos Marrons/efeitos dos fármacos , Adipogenia/efeitos dos fármacos , Adipogenia/genética , Tecido Adiposo/efeitos dos fármacos , Animais , Diferenciação Celular/genética , Proliferação de Células/efeitos dos fármacos , Dexametasona/administração & dosagem , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacos , Indometacina/administração & dosagem , Insulina/administração & dosagem , Insulina/metabolismo , Camundongos , Tri-Iodotironina/administração & dosagem , Tri-Iodotironina/metabolismo
3.
J Food Sci Technol ; 50(4): 826-9, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24425989

RESUMO

A paper chromatographic method for the detection of adulteration of anionic detergent in milk is described. The method is based on the complexing of anionic detergent with methylene blue dye and separation of complex from free dye using simple paper chromatographic method. Since complexing of detergent is with dye, visualization is direct without involvement of subsequent detection of complex. The method is simple and results are available in 10 min. The method is sensitive to detect 0.1 % (w/v) labolene (laboratory grade detergent) or 0.01 % (w/v) sodium dodecylbenzene sulfonate (pure anionic detergent) in milk. The method can be adopted at quality control laboratories in dairies for ascertaining the quality of milk.

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