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美國Pacific Biosciences SMRT DNA測序儀

價  格:詢價

產(chǎn)  地:美國更新時間:2020-09-29 16:31

品  牌:PacBio型  號:SMRT

狀  態(tài):正常點擊量:2130

400-006-7520
聯(lián)系我時,請說明是在上海非利加實業(yè)有限公司上看到的,謝謝!

上海非利加實業(yè)有限公司

聯(lián) 系 人: 上海非利加實業(yè)有限公司

電   話: 400-006-7520

傳   真: 400-006-7520

配送方式: 上海自提或三方快遞

聯(lián)系我時請說在上海非利加實業(yè)有限公司上看到的,謝謝!



該測序儀的工作原理是,將基因組的DNA斷開成許多很小的片段,這些小DNA片段制成溶液后滴入測序儀內(nèi)的金屬薄片上,金屬薄片中分布著3000個納米***小孔,這些納米孔的直徑不到70納米,被滴入薄片上后,小DNA片段會分散到不同的納米孔中。每個納米孔中涂有***種特殊的酶——DNA聚合酶,DNA聚合酶的特性是,能夠沿著DNA片段的雙鏈結(jié)構(gòu)游動,在游動的過程中將DNA片段的雙鏈結(jié)構(gòu)打開,分成兩個片段,也可為某個DNA單鏈找到對應(yīng)的片段,重新組合在***起,科學(xué)***將DNA聚合酶的作用形象地比喻成衣服的拉鏈,可開可合。

太平洋生物科學(xué)公司的測序儀就是利用DNA聚合酶來“竊取人類的自然本性”的。***旦DNA片段在納米孔中分散完畢,向聚合酶分子滴入經(jīng)過特殊處理的核苷酸溶液,謎底就會被揭開。核苷酸溶液中的每個核苷酸都用磷光染色劑做過標(biāo)記,金屬薄片的底部也有***個縮微版光譜儀,***旦DNA片段中有核苷酸與之配對,標(biāo)記物就會發(fā)出特定顏色的光,縮微版光譜儀就能檢測并記錄下這些閃光,測序儀從而記錄下每個DNA片段中的堿基對順序。當(dāng)閃光記錄完之后,結(jié)果會輸入計算機中,計算機破譯出所有的DNA片段結(jié)果,并重新“組裝”,讓基因組恢復(fù)原樣。

該樣機目前的測序速度為每秒鐘10個堿基對,2013年上市的測序儀將達到每秒測定1萬個堿基對的速度。盡管有來自其他諸多生物技術(shù)公司的激烈競爭,太平洋生物科學(xué)公司堅信,在資金雄厚的風(fēng)險投資公司的強有力支持下,自己公司的產(chǎn)品必將成為第***個上市的快速便宜的個人基因組測序儀。分析人士也激動地將太平洋生物科學(xué)公司比喻成“健康產(chǎn)業(yè)的谷歌”,公司將在未來的健康領(lǐng)域無處不在。


產(chǎn)品參數(shù)

SMRT? (Single Molecule Real Time) Biology is the application of Pacific Biosciences’ transformative detection platform to the real-time monitoring of biological processes at single molecule resolution and in specific, relevant contexts. This revolutionary strategy enables scientists to obtain a more complete characterization of the molecular interactions that define cellular processes. Essential to SMRT Biology are advanced informatics techniques that can integrate these high-dimensional data and enable the creation of richly informative models depicting interdependent relationships in living systems.

“Solving the puzzle of complex diseases, from obesity to cancer, will require a holistic understanding of the interplay between factors such as genetics, diet, infectious agents, environment, behavior, and social structures.”

Elias Zerhouni

The NIH Roadmap, Science 302:63-64 (2003).

Why is it Important?

Complex biological systems are dynamic, highly modular, and adaptive systems able to reconfigure themselves as conditions demand. The scientific community is increasingly recognizing that multiple data sources (e.g., DNA, RNA, protein and metabolite levels, etc.) and sophisticated computational approaches that integrate diverse data are required to uncover the hierarchy of molecular, cellular, and tissue based networks defining complex physiological and disease states.

While a significant technological revolution in biology has led to this realization, limitations in the available technologies have hampered the ability to embrace this scale of complexity. In order to fully realize the promise of personalized medicine, scientists require a means to obtain a comprehensive understanding of the fundamental building blocks of biological systems.(Figure 17)

Figure 17.

Pacific Biosciences’ Solution

Pacific Biosciences has developed a transformative technology platform for real-time detection of biological events at single molecule resolution. The first commercial application for this platform is DNA sequencing (available in 2010). Pacific Biosciences has begun expanding internal research programs and developing collaborations for additional ‘SMRT Biology’ applications and bioinformatics tools that will allow scientists to acquire new, fundamental knowledge about the molecular dynamics of life. These include simpler and more direct solutions for RNA sequencing, methylation sequencing, and even the largely uncharted real-time observation of protein translation.

DNA Sequencing

SMRT? DNA Sequencing offers very long reads, ultra-fast cycle times, and the flexibility to cost-effectively perform small or large projects. Because the SMRT DNA sequencing system provides temporal information about every base incorporation event, it can measure the kinetics of the enzyme independently for each base in a DNA sequence. The kinetics of incorporation are sensitive to, for example, the methylation status of the DNA template being sequenced. SMRT sequencing will unify the formerly separate applications of real-time, single-molecule DNA sequencing and methylation sequencing. This creates the potential to visualize methylation status and other epigenomic markers as a by-product of ordinary DNA sequencing with no change in sample preparation or run conditions. SMRT sequencing will unify the formerly separate applications of DNA sequencing and methylation sequencing. In addition, elimination of the bisulfite conversion step will save time and money as well as avoid the deleterious effects of conversion.

Read more about SMRT Sequencing for Resequencing and DeNovo applications

RNA Sequencing

Currently, the majority of nucleic acid sequencing is based on DNA, requiring RNA to be converted to cDNA prior to analysis. This can result in conversion bias, generation of spurious chimeras, and additional time and cost. Through the use of an RNA-dependent polymerase (such as a reverse transcriptase), RNA can be sequenced directly using the SMRT sequencing paradigm. Through the use of an RNA-dependent polymerase (such as a reverse transcriptase), RNA can be sequenced directly using the SMRT? sequencing. With the long readlength inherent in SMRT sequencing and no conversion bias, the polynucleotide structure of individual transcripts will be available for the first time without the need to rely on paired ends and inferences made across many molecules.

Other Applications of SMRT Biology

We expect numerous other applications of SMRT Biology will emerge. Pacific Biosciences is incubating academic research in other methods that will benefit from the SMRT Biology detection platform. For example, the machinery of protein synthesis, the ribosome, is another molecular apparatus that works from a template and performs cyclical additions based on nucleic acid sequence. By using fluorescent-labeled tRNAs, ribosomes can be observed in the same way polymerases are in SMRT DNA sequencing. By using fluorescent-labeled tRNAs, ribosomes can be observed in the same way polymerases are in SMRT DNA sequencing. As a piece of RNA is translated by the ribosome, the identity of the synthesized protein can be established by observing the sequence of tRNAs delivering amino acids to the ribosome. This will allow direct observation of protein synthesis over the entire proteome, without dependence on mRNA expression profiles.

In addition, because the system tracks temporal information, such studies will reveal the time-dependence of regulatory processes such as siRNA binding. By making the SMRT Biology technology available to the academic community, we expect numerous other uses of the system will be revealed. We encourage researchers to contact us to gain access to the SMRT Biology platform.

SMRT Informatics

The SMRT Biology platform will generate unprecedented scales and diversity of data on a daily basis. For example, from a single blood sample, scientists could produce a complete genome sequence, as well as a complete characterization of the RNA transcriptome, methylation patterns, and an assessment of the translational efficiencies in each individual cell type that can be isolated from blood. This will produce tens to hundreds of terabytes of data per sample.

Pacific Biosciences is developing an environment in which scientists can seamlessly integrate multiple data types from multiple sources and deploy advanced bioinformatics methods to elucidate the complexity of living systems. Therefore, we are committed to providing users with access to the right types of high-performance computing (HPC) environments to not only store and organize the data, but to enable analyses of the data on multiple different levels, from assembly of genomes to the construction of predictive models of disease. For example, we will provide cloud-based computing as one type of HPC service that leverages massive-scale compute environments in order to meet intense data storage and computational needs.

These informatics solutions will be designed to efficiently represent that magnitude of data and make it accessible not only to high-end informatics researchers, but also to biologists, clinicians and even patients. We believe this integration of real time biological data at single molecule resolution will be instrumental to in making personalized medicine a reality.


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