Chapitre 3 Migration par les RhoGTPases
4.3 I NTERACTIONS ACTO - MYOSINES
4.3.4 Utilisation de drogues
Assim, a partir deste estudo, tem-se, por exemplo, como possibilidades de investigações futuras:
• Desenvolver estudo de nucleação e crescimento de policristais de cera epicuticular, em superfícies cristalinas auto-organizadas;
• Aperfeiçoar metodologias biomiméticas para transferência desta tecnologia em escala industrial;
• Aprimorar novas técnicas de caracterização da molhabilidade de materiais biológicos, visando contribuir para o aperfeiçoamento de ensaios de medição do ângulo de contato e tensão superficial.
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9 ANEXOS ANEXO I
Elaborado pelo CENTRO DE MICROSCOPIA DA UFMG:
PROTOCOLO DE PREPARAÇÃO DE AMOSTRAS –VEGETAIS PARA MEV
Jogar os fragmentos da amostra no fixador primário modificado: * Karnovsky (2,0% paraformaldeído e 2,5% glutaraldeído), em tampão fosfato 0,1M por no mínimo 1h;
Remover o fixador e lavar as amostras 3X (10 minutos) em tampão fosfato 0,1M;
(1) Imergir as amostras no fixador secundário** por 1 hora; (**tetróxido de ósmio 1,0%). (2) Lavar novamente as amostras por 3X (10 minutos) em tampão fosfato 0,1M;
(3) Imergir as amostras em Ácido Tânico 1% em tampão fosfato 0,1M por 20 minutos. (4) Lavar novamente as amostras por 3X (10 minutos) em tampão fosfato 0,1M;
(5) Imergir as amostras no fixador secundário** por 1 hora; (**tetróxido de ósmio 1,0% ). (6) Lavar novamente as amostras por 3X (10 minutos) em água destilada.
(7) Desidratar as amostras em solução crescente de Álcool etílico 50% a 95% (10 minutos) e em 100% (3X-10 minutos).
(8) Realizar a secagem das amostras no ponto crítico de CO2
(9) Montar as amostras nos stubs usando cola de carbono ou prata , posicionando a folha para cima (face superior), deixar secar em estufa a 400 overnight.