<a href="https://www.jove.com/video/50255">Apresentando uma caixa de corte ajustável ângulo para analisar Slice força de cisalhamento na carne</a> <a href="/author/Tom_Whitesell" rel="author">Tom Whitesell</a> 1, <a href="/author/Carmen_Avil%E9s" rel="author">Carmen Avilés</a> 2, <a href="/author/Jennifer+L._Aalhus" rel="author">Jennifer L. Aalhus</a> 1, <a href="/author/Chris+R._Calkins" rel="author">Chris R. Calkins</a> 3, <a href="/author/Ivy+L._Larsen" rel="author">Ivy L. Larsen</a> 1, <a href="/author/Manuel_Ju%E1rez" rel="author">Manuel Juárez</a> 1 Força de cisalhamento Slice é um método de referência para análise de textura de carne. Usando uma caixa de corte de ângulo ajustável poderia aumentar a sua precisão para fins de pesquisa. Os resultados de diferentes locais dentro do músculo Longissimus mostram uma alta correlação com a metodologia vigor Warner-Bratzler sheare alto potencial de adaptabilidade para diferentes músculos. <a href="https://www.jove.com/video/50331">Imagem tridimensional de nociceptivos Fibras Nervosas intraepidérmicos em biópsias de pele humana</a> <a href="/author/Jacqueline_Dauch" rel="author">Jacqueline Dauch</a> 1, <a href="/author/Chelsea_Lindblad" rel="author">Chelsea Lindblad</a> 1, <a href="/author/John+M._Hayes" rel="author">John M. Hayes</a> 1, <a href="/author/Stephen+I._Lentz" rel="author">Stephen I. Lentz</a> 2, <a href="/author/Hsinlin+T._Cheng" rel="author">Hsinlin T. Cheng</a> 1 A fim de estudar as alterações de fibras nervosas intra-epidérmica nociceptivos (IENFs) em neuropatias dolorosas (PN), protocolos que nós desenvolvemos pode examinar directamente as alterações morfológicas observadas tridimensionais em IENFs nociceptivos. Análise tridimensional de IENFs tem o potencial para avaliar o ch morfológica<html> anges de IENF na PN. <a href="https://www.jove.com/video/50451">Microscopia de fluorescência de campo amplo e Fluorescente imagem Citometria de Fluxo em um telefone celular</a> <a href="/author/Hongying_Zhu" rel="author">Hongying Zhu</a> 1, <a href="/author/Aydogan_Ozcan" rel="author">Aydogan Ozcan</a> 1,2,3 Nós revisamos nossos resultados recentes sobre a integração da microscopia de fluorescência e ferramentas de citometria de fluxo de imagem em um telefone celular usando anexos opto-fluídicos compactos e de baixo custo. Dispositivos de micro-análise destes telefone celular com base pode ser útil para análise por citometria, como executar várias tarefas de contagem de células, bem como para high-throughput screening de, por exemplo, amostras de água em ambientes com recursos limitados. <a href="https://www.jove.com/video/3194">Isolamento e Cultura da crista neural células-tronco de folículos de cabelo humano</a> feng_Yang &quot;rel =&quot; autor &quot;&gt; Ruifeng Yang, <a href="/author/Xiaowei_Xu" rel="author">Xiaowei Xu</a> Este artigo apresenta um protocolo robusto para isolamento e cultivo de células-tronco da crista neural de folículos capilares humanos.

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april 2013: this month in jove

Aqui está um olhar para o que está chegando na abril 2013 edição do Journal of Experiments visualizar (Jove). Geralmente não é permitido ter comida em laboratórios por causa de problemas de contaminação e consequências potencialmente perigosos pesquisa. No entanto, este mês, Jove apresenta um artigo de vídeo que envolve a carne cozinhar em laboratório. <a href="http://www.jove.com/video/50255">Whitesell et al.</a> apresentar um método para medir a maciez da carne cozida, que é uma preocupação significativa na indústria de carne bovina. Por causa do ângulo das fibras de carnes pode afectar a força de cisalhamento, os autores utilizam uma caixa de corte de ângulo variável, o que lhes permite cortar a carne de modo a fatia é paralela às fibras musculares. Isso permite medições precisas da força máxima necessária para cortar um bife. Em outro artigo, passamos de carne de amostras de pele humana, como as que sobraram de procedimentos facelift. Folículos pilosos Contaem muitos tipos diferentes de células estaminais, de modo <a href="http://www.jove.com/video/3194">Yang e Xu</a> demonstrar como para extrair os folículos de cabelo a partir de amostras de pele e isolar células estaminais da crista neural (NCSCs) utilizando separação de células activada por fluorescência (FACS). Os autores demonstram como os NCSCs cultura, o que pode, potencialmente, ser utilizados em medicina regenerativa. Em Medicina Clínica e Translacional Jove, temos outro artigo envolvendo amostras de pele humana. Descrito pela <a href="http://www.jove.com/video/50331">Dauch et ai.</a> , este procedimento utiliza imunohistoquímica em biópsias de pele humana para estudar as fibras nervosas intra-epidérmica na neuropatia dolorosa. A imagiologia tridimensional permite a visualização de modificações morfológicas (tais como edemas axonal) associados com neuropatias. Isso permite que os médicos a diagnosticar com precisão pequenas neuropatias fibra de soco biópsias de pele. Finalmente, na seção de Bioengenharia, Temos uma outra técnica de microscopia romance do grupo Ozcan na UCLA, que já publicou três artigos em Jove. O artigo mais recente, a partir de Agosto de 2012, demonstrou o uso de um sistema de lentes de imagem livre de glóbulos brancos num chip de microfluidos (veja <a href="http://www.jove.com/video/4161/lensfree-on-chip-tomographic-microscopy-employing-multi-angle">Isikman et al 2012.</a> ). No quarto artigo Jove do grupo, <a href="http://www.jove.com/video/50451">Zhu e Ozcan</a> demonstrar como anexar um microscópio de fluorescência de campo amplo opto-fluídico para qualquer câmera de telefone celular. As amostras líquidas são aplicados através de um canal microfluídico, e a câmara do telefone celular pode ser utilizado para gravar um vídeo das células que fluem através do canal. Este procedimento permite que as células marcadas com fluorescência a ser trabalhada e caracterizado com uma câmera de telefone celular compacto e de baixo custo, o que pode ser muito útil para diagnósticos point-of-care ou campo. Você acabou had uma pré-visualização de alguns dos destaques de Jove para o mês de abril. Visite o site para ver os artigos completos, além de muitas outras, em Jove: The Journal of Experiments visualizadas.

Watch this Scientific Journal Video about April 2013: This Month in JoVE at JoVE.com

April 2013: This Month in JoVE

Aqui estão alguns destaques da edição de abril 2013 Journal of Experiments visualizar (Jove).

Abril 2013: Este mês na JOVE

Here's a look at what's coming up in the April 2013 issue of Journal of Visualized Experiments (JoVE).
It's usually not permissible to have food in ...

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7.7K visualizações.  Massachusetts Eye and Ear. Aqui estão alguns destaques da edição de abril 2013 Journal of Experiments visualizar (Jove).

Vídeo: April 2013: This Month in JoVE

August 2012: This Month in JoVE

Traditional microscopy requires lens objectives to magnify specimens, and can involve numerous optical components like additional objectives, filters, and mirrors to refract and direct light to optical sensors. The August 2012 issue of JoVE (Journal of Visualized Experiments) is marked by the third publication from the Ozcan Lab (University of California, Los Angeles) on their lens free lens-free "on-chip" microscopy platform, which they have pioneered.
Back in 2009, the Ozcan lab published their first article, which demonstrated the use of a lens-free imaging platform that could image cells within whole blood. This imaging technique involves placing a sample directly on an optoelectric sensor array, like the CCD or CMOS chips found in the standard camcorder. Then, LED illumination from above the sample casts shadows on the chip, which are recorded as digital holograms that can be subjected to image processing. Not only does this lensless imaging system allow for an extremely large field of view (FOV of 0.6-8 cm2), the lack of bulky optical components makes it excellent for microfluidic applications. The Ozcan group demonstrates this in their follow-up 2011 JoVE article, in which fluorescently labeled white blood cells are imaged within a microfluidic chip.
This August in JoVE, the Ozcan group demonstrates further advancements to their lens-free microscopy platform by applying it to tomographic imaging of the nematode, C. elegans. By changing the angle of illumination, using a motorized rotation stage, the Ozcan group shows how multiple holographic slices may be generated for a sample-which, following processing, can be combined into tomograms. The Ozcan group confirms that their 3D reconstruction of the worm is successful by citing that the pharyngeal tube, a 5-micron-thick structure, is only visible in a single slice and in a 3D reconstructed cross section.
The compact and inexpensive nature of the lens-free imaging systems - designed and assembled by the Ozcan group - make them well suited for point-of-care diagnostic applications, or even cell phone based microscopy that can be performed in the field.
At the Ernest Gallo Clinic and Research Center at University of California, San Francisco JoVE learns how to visualize morphological changes in single cells using three-dimensional fluorescence microscopy and computer analysis. In this procedure, cells are given agonist, antagonist plus agonist, or no treatment, and prepared for immunofluorescence microscopy. Three-dimensional images are acquired with the help of a two-photon laser system, and the fluorescence data are processed on the computer using Imaris and Matlab.
To demonstrate the power of this technique, our authors quantify single-cell phenotypic changes in transfected HEK293 cells. Three-dimensional morphometric analysis shows dramatic changes in cells treated with agonist. These changes are not always apparent when using conventional 2D analysis. This technique allows morphological changes in single cells to be quantified and characterized in response to pharmacologic stimuli, offering a powerful new assessment tool to the arsenal of drug discovery research.
This month, in JoVE Applied Physics, we travel to South Carolina to visit the School of Materials Science and Engineering at Clemson University. Here, researchers show us how to construct lithium batteries for laboratory research.
The basic components of a lithium coin cell are the working electrode, the lithium electrolyte, and a lithium foil counter electrode. The different components of the coin cell are carefully assembled and sealed with a crimping machine. The finished coin cell can then be characterized in a battery tester. Using their homemade coin cells, our researchers can experiment with using different materials to make the cathodes of lithium coin cells.
This month in JoVE Immunology and Infection, we head to Basel, Switzerland to witness two techniques for diagnosing helminth infections. We also see how investigators perform the shuttle run test in children, in order to assess the effects of these infections on physical fitness.
Helminths are parasitic worms that can live inside humans and animals. Many species infect the intestinal tract, and may be transmitted through soil. Our authors demonstrate the Kato-Katz technique, which is used for diagnosing several common soil-transmitted helminths. They also demonstrate the Baermann technique, which uses light to stimulate the migration of certain types of phototactic helminths out of sample preparations. The various types of helminth species can subsequently be determined based on morphology.
Our authors then demonstrate how to set up and perform a 20-meter shuttle run test for children, and to measure the impact of helminth infections on physical fitness. This method can help determine the true burden of soil-transmitted helminth infections on overall health.
This brief summary highlights but a few notable video-articles that will be released in August. We'll also feature articles that demonstrate how to express genes in the midbrain of the chick embryo, study neutrophil transmigration in parallel flow chambers lined with endothelial cells, and precisely measure proteolytic degradation of the extracellular matrix.

Traditional microscopy requires lens objectives to magnify specimens, and can involve numerous optical components like additional objectives, filters, and mirrors to refract and direct light to optical sensors. The August 2012 issue of JoVE (Journal of Visualized Experiments) is marked by the third publication from the Ozcan Lab (University of California, Los Angeles) on their lens-free "on-chip" microscopy platform, which they have pioneered.

Agosto 2012: Este mês na JOVE

Traditional microscopy requires lens objectives to magnify specimens, and can involve numerous optical components like additional objectives, filters, and ...

Research

JoVE Journal

Biologia

2012: A Year In Review

Here's a look at some of the milestones and highlights of the year 2012 in Journal of Visualized Experiments (JoVE).
At the start of 2012, JoVE reached a major milestone by publishing our 1500th article. In this publication, in JoVE Bioengineering, Yu et al. described a method for analyzing the free radical composition of cigarette smoke. This method simulated cigarette puffing with a single-port smoking device, and combined it with electron spin resonance (ESR) spectroscopy to measure the degree to which antioxidant compounds can scavenge free radicals in cigarette smoke. A possible outcome of this research is the creation of less harmful cigarettes.
JoVE Bioengineering also contained the most-viewed article of 2012. Owczarczak et al. described a method for hacking a standard inkjet printer, loading ink cartridges with a cell-suspension "bioink," and printing lines of live cells onto glass slides. The thermal inkjet printing process creates temporary pores in the cell membrane, visualized by the incorporation of fluorescently labeled actin monomers. This concept, called "bioprinting," has many potential applications in cell and tissue engineering.
Also in 2012, JoVE Bioengineering featured a protocol by Hsia et al. for isolating and purifying spider silk protein, spinning it into fibers, and assessing the fiber strength. This protocol for laboratory-scale production of spider silk, which is stronger than tensile steel, can potentially be extended to large-scale manufacturing.
In JoVE Clinical and Translational Medicine, we featured a number of articles related to stroke, one of which. In one article, M&ouml;bius-Winkler et al. demonstrated placement of the WATCHMAN left atrial appendage occlusion device from Boston Scientific. This device is designed to prevent strokes by trapping clots within the left atrial appendage of the heart before they exit. Our authors demonstrated how to insert the guide wire through the femoral artery into the heart, advance the device into the left atrium, and deploy the device in the left atrial appendage.
Another article focused on stroke, Hamel et al. described the use of a driving simulator to study how patients compensate for visual field defects following stroke. By analyzing the compensatory gaze behavior of patients as they navigated through virtual driving courses with varying degrees of complexity, our authors see great potential for the use of driving simulators in stroke rehabilitation.
In JoVE Immunology and Infection, we published an article by Keyel et al. describing the real-time kinetics of immune cell responses to bacterial toxins using live cell microscopy. Combined with high-speed 3D confocal microscopy, this technique can also visualize the cellular repair response.
Also in JoVE Immunology and Infection, we featured an article by Yap et al. describing methods for diagnosing helminth infections in children. Helminths are parasitic worms that can infect the intestinal tract of humans and animals, and may be distinguished based on their morphology. The same article demonstrated how to measure the impact of helminth infections on physical fitness in children, which is a measure of overall health.
In JoVE Neuroscience, we featured a method by Hoffmann et al., who used tiny headphones to alter the auditory feedback in songbirds, and analyzed the computational and neurophysiological basis of vocal learning in birds when they adjust their singing in response to altered acoustic signals.
Also in JoVE Neuroscience, we moved from birds to bees with a method that assesses associative and non-associative tactile learning in honeybees. This method, by Mujagi&#263; et al., allowed bees to scan different metal surfaces with their antennae, then conditioned them to expect sugar water when their antennae touched particular surfaces, and analyzed the corresponding changes in antennal movement.
In 2012, we launched a brand-new section: JoVE Applied Physics, which features articles on subjects ranging from plasma physics to material science. The Applied Physics section also contained JoVE's 2000th video article, filmed in a synchrotron radiation facility, where Borisenko et al. showed how to determine the electronic structure of complex materials using angle-resolved photoemission spectroscopy.
In the JoVE General section, we published an article by Artioli et al. demonstrating the use of a portable gas analyzer to measure oxygen consumption during complex exercise - such as judo. By analyzing oxygen consumption and collecting blood for measuring plasma lactate concentration, this method can determine the relative contributions of different energy systems to specific aspects of complex exercise.
Finally, JoVE followed Dolhi et al. to a permanently ice-covered saline lake in Antarctica. There, scientists drilled through the ice to study single-celled microorganisms called protists that live in the harsh conditions of Antarctica.
This Year in Review was just a brief glimpse of a few of over 600 video articles that JoVE offered in 2012. Browse the JoVE archives to see thousands of other videos, and stay tuned for what's coming up this year in JoVE: The Journal of Visualized Experiments.

Here's a look at some of the milestones and highlights of the year 2012 in Journal of Visualized Experiments (JoVE).

2012: Um ano em análise

 
 
Here's a look at some of the milestones and highlights of the year 2012 in Journal of Visualized Experiments (JoVE).
At the start of 2012, JoVE ...