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廣州健侖生物科技有限公司>>人類疾病診斷>>基因檢測(cè)>> MAF/IGH融合基因t(14;16)探針
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MAF/IGH融合基因t(14;16)探針

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  • 廣州健侖生物科技有限公司
  • 2018-03-01 09:14:59
  • 廣州市
  • 廣州
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MAF/IGH融合基因t(14;16)探針

本試劑盒主要用于MAF/IGH融合基因t(14;16)的檢測(cè),里面包括即用型雜交液和DAPI復(fù)染劑。
本試劑盒僅供科研使用。

【詳細(xì)說(shuō)明】

MAF/IGH融合基因t(14;16)探針

 

 廣州健侖生物科技?有限公司 

本司長(zhǎng)期供應(yīng)尼古?。商鎸帲z測(cè)試劑盒,其主要品牌包括美國(guó)NovaBios、廣州健侖、廣州創(chuàng)侖等進(jìn)口產(chǎn)品,國(guó)產(chǎn)產(chǎn)品,試劑盒的實(shí)驗(yàn)方法是膠體金方法。

我司還有很多熒光原位雜交系列檢測(cè)試劑盒以及各種FISH基因探針和染色體探針等,。

MAF/IGH融合基因t(14;16)探針

   本試劑盒主要用于AML1/ETO融合基因t(8;21)的檢測(cè),里面包括即用型雜交液和DAPI復(fù)染劑。
本試劑盒僅供科研使用。

  

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以下是我司出售的部分FISH產(chǎn)品:

 

6號(hào)染色體計(jì)數(shù)探針(綠色)
8號(hào)/20q探針
D13S25(13q14)探針(紅色)
JAK2(9p24)基因斷裂探針
FRS2(12q15)基因探針
p53/RB1/ATM/CSP12/D13S25/6/6q21/IGH基因探針(七探針 )
MYC(8q24),BCL6(3q37),BCL2(18q21)探針
API2/MALT1融合基因t(11;18)探針
MALT1/IGH融合基因t(14;18)探針
IGH融合基因(CCND1,MAF,MAFB,FGFR3)探針
ALK、MET、ROS1基因探針
FGFR1,PDGFRA,PDGFRB基因探針
7號(hào)/8號(hào)染色體探針
8號(hào)/17號(hào)染色體探針
8號(hào)染色體計(jì)數(shù)探針(紅色)
D7S522(7q31)基因探針
RB1(13q14)/ATM(11q22)基因探針

 

MAF/IGH融合基因t(14;16)探針

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【公司名稱】 廣州健侖生物科技有限公司
【】    楊永漢 

【】
【騰訊 】
【公司地址】 廣州清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號(hào)二期2幢101-3室

【企業(yè)文化宣傳】MAF/IGH融合基因t(14;16)探針

 

 

生殖細(xì)胞負(fù)責(zé)遺傳信息的時(shí)代傳遞,那么基因組的完整性對(duì)于生殖細(xì)胞至關(guān)重要。而在真核生物精細(xì)胞中,有許多外來(lái)侵入的轉(zhuǎn)座子、逆轉(zhuǎn)座子等移動(dòng)型遺傳元件。這些自私的遺傳元件在染色體不同位點(diǎn)間跳躍,造成基因突變和基因組損傷。在生殖細(xì)胞中,轉(zhuǎn)座子的跳躍可能會(huì)導(dǎo)致不育。PiRNA/Piwi能夠高效的阻止轉(zhuǎn)座子等元件對(duì)基因組的損傷。研究發(fā)現(xiàn),piRNA起源于反轉(zhuǎn)座子、重復(fù)序列等區(qū)域,與Piwi蛋白形成piRNA/Piwi機(jī)器,沉默轉(zhuǎn)座子、反轉(zhuǎn)座子等。此外,piRNA還可以發(fā)揮類似于siRNA的功能,參與調(diào)控生殖細(xì)胞中編碼基因的表達(dá)。

方法:

研究人員發(fā)現(xiàn)無(wú)精子癥患者體內(nèi)Piwi(Hiwi)生殖突變會(huì)阻止其泛素化和降解。為了了解其中的作用機(jī)制,研究人員構(gòu)建了Piwi(Miwi)突變敲入小鼠模型,證明了這種遺傳缺陷直接導(dǎo)致了男性不育癥。具體來(lái)說(shuō),研究人員發(fā)現(xiàn)MIWI能以一種對(duì)立于Piwi作用RNA(piRNA)的方式,與組蛋白泛素連接酶RNF8結(jié)合,并在晚期精子細(xì)胞的細(xì)胞質(zhì)中穩(wěn)定螯合RNF8,從而導(dǎo)致精子異常,引起組蛋白滯留,形態(tài)異常和活性嚴(yán)重受損,而這可以通過(guò)RNF8-N阻斷精子細(xì)胞中RNF8-MIWI的相互作用,逆轉(zhuǎn)功能。

研究人員篩查了413例臨床無(wú)精、弱精癥患者Piwi基因上控制Piwi蛋白泛素化修飾降解的關(guān)鍵元件D-box,發(fā)現(xiàn)有3例病人在此元件中存在雜合性基因突變,且發(fā)現(xiàn)此類突變可來(lái)源于基因自發(fā)突變,也可從母親遺傳獲得。為鑒定此類突變是否是造成這些患者發(fā)生無(wú)精/少弱精的原因,研究人員將其中的一組突變條件型敲入小鼠Piwi基因,在小鼠模型中研究此類突變對(duì)精子發(fā)生的作用。他們發(fā)現(xiàn), Piwi D-box雜合突變小鼠均出現(xiàn)雄性不育,精子表型也與患者*。深入研究發(fā)現(xiàn),Miwi D-box雜合突變小鼠精子發(fā)生阻滯在延長(zhǎng)型精子細(xì)胞發(fā)育階段,盡管能產(chǎn)生少量精子,但精子形態(tài)異常、細(xì)胞核結(jié)構(gòu)疏松、無(wú)活力。

機(jī)制研究揭示, PIWI蛋白具有將RNF8“扣留”于細(xì)胞核外的功能。正常小鼠體內(nèi)PIWI蛋白會(huì)在精子發(fā)育后期被自然降解,RNF8進(jìn)入細(xì)胞核內(nèi)開(kāi)啟“組蛋白-魚精蛋白轉(zhuǎn)換”,幫助精子發(fā)育完成。而Piwi蛋白突變導(dǎo)致其在后期不能被正常代謝,大量RNF8因此被“扣留”在細(xì)胞核外,魚精蛋白與組蛋白交換受阻,zui終造成精子發(fā)育受阻。將RNF8-N端導(dǎo)入突變小鼠的精子細(xì)胞后,可有效阻斷Piwi基因蛋白產(chǎn)物對(duì)RNF8的“扣留”,恢復(fù)精子的正常形態(tài)及游動(dòng)能力,提示該策略對(duì)臨床治療此類無(wú)精、弱精癥具有重要理論參考價(jià)值。

  

According to foreign media reports, an international research team led by Dirk Schulze-Makuch, Washington State University, found that the most Spartan, seemingly lifeless place on the earth's surface is not so lifeless. Once considered or even lack of microbes, the Atacama Desert showed special bacteria reproduction after rainfall. This indicates that there may be similar "dormancy" groups on red planet.

 


Atacama Desert is thought to be the earth's closest natural environment to Mars. The living environment of the Chilean desert is so bad that even bacteria can not survive under normal conditions. The rainfall here is measured in millimeters per ten years. Although the 10 million - year history of the desert Mediterranean climate is surprising, there is not enough water to sustain life. Worse, cold temperatures mean less energy that can be used for growth and reproduction.

According to Schulze-Makuch, when the Washington State University's research began in 2015, the unanimate reputation seemed to be intact. Although they found some microbes and DNA traces in Atacama Desert, these residues were proved to come from the outside world.

When the desert first came to rain for decades, the situation changed. It activated the long time dormant biological groups buried under the surface. These groups made full use of a short chance to reproduce. When the research team returned in 2016 and 2017, they found that these populations were gradually dormant when the soil dried up. However, they obtained uncontaminated samples by using sterilized spoon and special instruments, and identified several kinds of local microbial species by genome analysis.

 


"In the past, researchers have found dead organisms and DNA residues near the surface, but this is the first discovery of persistent life forms in the soil of Atacama Desert," Schulze-Makuch said. "We believe that these microbial communities can be dormant for hundreds of years or even thousands of years on very similar conditions found on planets like Mars, and then return to life when it rains."

Schulze-Makuch believes that the impact on Mars research is quite large.  Though the environment of Mars is so desolate now, billions of years ago, this place is a very different place. There are shallow seas, rivers and lakes, and simple living things have evolved. As Mars becomes colder and drier, it is possible to adapt to some forms of life by long dormancy.

"We know that the water in the Martian soil is frozen, and recent studies strongly show that the night rain and other increased humidity events near the surface," Schulze-Makuch said. "If life has evolved on Mars, our research shows that it may be alive under the dry surface of today."

The Washington State University's research team is scheduled to return to Atacama Desert in March 15th for another two weeks of investigation, which may involve the discovery of more microorganisms. "There are only a few places left on the planet to find new forms of life that can survive on that environment on Mars," Schulze-Makuch said. Our goal is to understand how they do this so that we know what to look for on the surface of Mars. "

    
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