摘要:
The present invention relates to optoelectronic devices based on a perovskite material comprising organic passivation agents for reducing unwanted recombination effects and to a method of producing such.In particular the invention relates to PeLED with exceptional high EQE up to 21.6%.
摘要:
Described are computer-based methods and apparatuses, including computer program products, for scalable seamless digital video stream splicing. Data packets in a first video stream of bits are rearranged. Placeholder packets are created in a second video stream of bits. The first video stream of bits and the second video stream of bits are combined to generate a spliced stream by inserting data packets from the first video stream of bits into the placeholder packets in the second video stream of bits.
摘要:
A rapid test kit may have a genetic probe, and antibody detecting probe or a combination of a genetic probe and an antibody detecting probe disposed within one or more test windows of the test kit. A cellulose filter paper membrane with a flow rate selected in a range of about 0.04 to about 0.4 ml/min/cm2 is used in one example, The test kit provides for rapid screening for DNA, RNA or fragments of DNA or RNA in a bodily fluid or antibodies indicating exposure to such DNA/RNA. The genetic probe may include single stranded DNA or a fragment of single stranded DNA, such as primer, immobilized on the filter paper, and a single stranded DNA, such as the same or a different primer, conjugated with a marker, such as a nanotube or nanoparticle. For example, a gold nanoparticle or a carbon nanotube may be used as a staining agent by conjugating the gold nanoparticle or the carbon nanotube to a genetic probe, such as a DNA primer capable of binding with a complementary DNA or viral RNA or a fratment of one of these. By comparing contrast or intensity of a test spot to a standard, a viral load may be reported. By comparing a test region using the genetic marker and a test region using an antigen to detect antibodies, a sensitive and specific test may be conducted during use of a vaccine to determine the effectiveness of the vaccine, for example.
摘要翻译:快速测试试剂盒可以具有遗传探针和抗体检测探针,或者位于测试试剂盒的一个或多个测试窗口内的遗传探针和抗体检测探针的组合。 在一个实施例中使用流量选择在约0.04至约0.4ml / min / cm 2范围内的纤维素滤纸膜。测试试剂盒提供对身体的DNA,RNA或DNA或RNA片段的快速筛选 表明暴露于这种DNA / RNA的液体或抗体。 遗传探针可以包括固定在滤纸上的单链DNA或单链DNA片段,例如引物,以及与标记物如纳米管缀合的单链DNA,例如相同或不同的引物 或纳米颗粒。 例如,金纳米颗粒或碳纳米管可以通过将金纳米颗粒或碳纳米管与遗传探针(例如能够与互补DNA或病毒RNA结合的DNA引物)或遗传探针结合的染色剂用作染色剂 其中之一。 通过将测试点的对比度或强度与标准进行比较,可以报告病毒载量。 通过比较使用遗传标记的测试区域和使用抗原的测试区域来检测抗体,例如,可以在使用疫苗期间进行敏感和特异性测试以确定疫苗的有效性。
摘要:
This invention pertains to inhibitors of atrial natriuretic peptide receptor A (NPRA) function, such as small interfering RNA (siRNA), useful for reducing the inflammation associated with many human diseases, such as asthma, respiratory syncytial virus (RSV) infection, and cancers (such as melanoma, lung cancer, and/or ovarian cancer) by interfering with NPRA gene expression or otherwise reducing NPRA function within a subject; and methods for treating a subject suffering from, or at risk of developing, an inflammatory disease, respiratory allergy (such as allergic rhinitis and asthma), viral infection, and/or cancer by administering such NPRA inhibitors to the subject.
摘要:
A rapid test kit may have a genetic probe, and antibody detecting probe or a combination of a genetic probe and an antibody detecting probe disposed within one or more test windows of the test kit. A cellulose filter paper membrane with a flow rate selected in a range of about 0.04 to about 0.4 ml/min/cm2 is used in one example, The test kit provides for rapid screening for DNA, RNA or fragments of DNA or RNA in a bodily fluid or antibodies indicating exposure to such DNA/RNA. The genetic probe may include single stranded DNA or a fragment of single stranded DNA, such as primer, immobilized on the filter paper, and a single stranded DNA, such as the same or a different primer, conjugated with a marker, such as a nanotube or nanoparticle. For example, a gold nanoparticle or a carbon nanotube may be used as a staining agent by conjugating the gold nanoparticle or the carbon nanotube to a genetic probe, such as a DNA primer capable of binding with a complementary DNA or viral RNA or a fratment of one of these. By comparing contrast or intensity of a test spot to a standard, a viral load may be reported. By comparing a test region using the genetic marker and a test region using an antigen to detect antibodies, a sensitive and specific test may be conducted during use of a vaccine to determine the effectiveness of the vaccine, for example.
摘要翻译:快速测试试剂盒可以具有遗传探针和抗体检测探针,或者位于测试试剂盒的一个或多个测试窗口内的遗传探针和抗体检测探针的组合。 在一个实施例中使用流量选择在约0.04至约0.4ml / min / cm 2范围内的纤维素滤纸膜。测试试剂盒提供对身体的DNA,RNA或DNA或RNA片段的快速筛选 表明暴露于这种DNA / RNA的液体或抗体。 遗传探针可以包括固定在滤纸上的单链DNA或单链DNA片段,例如引物,以及与标记物如纳米管缀合的单链DNA,例如相同或不同的引物 或纳米颗粒。 例如,金纳米颗粒或碳纳米管可以通过将金纳米颗粒或碳纳米管与遗传探针(例如能够与互补DNA或病毒RNA结合的DNA引物)或遗传探针结合的染色剂用作染色剂 其中之一。 通过将测试点的对比度或强度与标准进行比较,可以报告病毒载量。 通过比较使用遗传标记的测试区域和使用抗原的测试区域来检测抗体,例如,可以在使用疫苗期间进行敏感和特异性测试以确定疫苗的有效性。
摘要:
The subject invention provides for the utilization of bone-marrow derived stem cells in the treatment of allergic and inflammatory diseases. In one embodiment, the invention provides for treatment of asthma. Bone-marrow derived stem cells can be used for decreasing inflammation and alter the course of immune response in the lung.
摘要:
The described invention provides genetically engineered microorganisms, including photosynthetic microorganisms, expressing 4-hydroxybenzoyl-CoA thioesterases and methods of using the genetically engineered microorganisms for producing free fatty acids and/or fatty acid derivatives.
摘要:
Described are computer-based methods and apparatuses, including computer program products, for input queued content switching using a playlist. A retrieval sequence is generated using a plurality of content requests based on content location information. A first portion of content is requested to be queued at a first content source, and a second portion of content is requested to be queued at a second content source. A content stream of the first portion and the second portion of content is generated using the retrieval sequence. The generating includes selecting the first portion of content from a queue associated with the first content source and transferring the first portion of content to an output buffer, then terminating transfer of the first portion of content and initiating transfer of the second portion of content from a queue associated with the second content source. The portion of content in the output buffer is transmitted to a client device.
摘要:
Methods, compositions and devices are provided by the present invention for reducing activity of a natriuretic peptide receptor and other signals. Therapeutic treatments are provided by use of polynucleotides encoding a natriuretic peptide or by regulating the expression of natriuretic peptide receptor, such as NPRA and NPRC, or combinations of these therapies. Routes used for delivering polynucleotides encoding a natriuretic peptide, or, for example, siRNA that down regulates natriuretic peptide receptor include subcutaneous injection, oral gavage, transdermal and intranasal delivery routes. Compositions can include chitosan. chitosan derivatives, and chitosan derivative and a lipid. Transdermal delivery can use a transdermal cream. Intranasal delivery can use a dropper or an aspirator for delivery of a mist. Oral gavage delivers equivalent to oral delivery. Delivery permits cell and tissue specific targeting of gene therapies resulting in expression of a natriuretic peptide or down regulation of natriuretic peptide receptor. A variety of cancers, asthma and viral diseases can be treated therapeutically using the methods and compositions of the present invention.
摘要:
This invention pertains to inhibitors of atrial natriuretic peptide receptor A (NPRA) function, such as small interfering RNA (siRNA), useful for reducing the inflammation associated with many human diseases, such as asthma, respiratory syncytial virus (RSV) infection, and cancers (such as melanoma, lung cancer, and/or ovarian cancer) by interfering with NPRA gene expression or otherwise reducing NPRA function within a subject; and methods for treating a subject suffering from, or at risk of developing, an inflammatory disease, respiratory allergy (such as allergic rhinitis and asthma), viral infection, and/or cancer by administering such NPRA inhibitors to the subject.