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AML/ETO融合基因檢測(cè)試劑盒 熒光原位雜交法

AML/ETO融合基因檢測(cè)試劑盒 熒光原位雜交法

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AML/ETO融合基因檢測(cè)試劑盒 熒光原位雜交法
本試劑盒主要用于白血病的AML/ETO融合基因的檢測(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。

  • 產(chǎn)品描述

AML/ETO融合基因檢測(cè)試劑盒 熒光原位雜交法

廣州健侖生物科技有限公司

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,。

    t(8;21)(q22;q22)是初治急性粒細(xì)胞白血病(AML)患者中常見的細(xì)胞遺傳學(xué)異常,大約20%~40%的AML-M2患者有t(8;21)(q22;q22),并且在M2b亞型中發(fā)生率高達(dá)90%以上。位于染色體21q22的AML1基因與8q22的ETO基因融合,產(chǎn)生AML1/ETO融合基因。AML1/ETO融合基因是轉(zhuǎn)錄激活基因,導(dǎo)致細(xì)胞不斷增殖。臨床上t(8;21)白血病好發(fā)于青年和兒童(5%~10%),主要與M2型密切相關(guān),并且年齡越小發(fā)生率越高。t(8;21)代表預(yù)后較好的急性白血病類型,成人患者對(duì)治療反應(yīng)佳,*緩解率高,中位生存時(shí)間長(zhǎng),但易復(fù)發(fā);兒童患者的治療和預(yù)后不如成人患者理想。AML1/ETO融合基因可作為M2b診斷分型的標(biāo)志,以及微小殘留病灶監(jiān)測(cè)的一項(xiàng)檢測(cè)手段。

AML/ETO融合基因檢測(cè)試劑盒 熒光原位雜交法

如需訂購或者了解請(qǐng)以下或

mob: 楊    

我司還提供:登革熱,黃熱病,基肯孔熱,西尼羅河,立次克體,無形體,蜱蟲,恙蟲,錐蟲,利什曼原蟲,RK39, 漢坦病毒,乙腦,森林腦炎,寨卡病毒 ,H7N9 ,流感,霍亂,軍團(tuán)菌,結(jié)核,諾如病毒,輪狀病毒,炭疽,O157,葡萄球菌 ,流行性出血熱,傷寒桿菌,志賀氏菌檢測(cè)試劑,! 

以下是我司出售的部分FISH產(chǎn)品:

p53/RB1/ATM/CSP12/D13S25基因探針
5q33/5q31/D7S486/D7S522/CSP8/D20S108/XY基因探針
4/10/17/KMT2A[ETV6RUNX1]/[BCRABL(DF)]基因探針
p53/D13S319/RB1/1q21/IGH基因探針
13/16/18/21/22/XY染色體計(jì)數(shù)探針
ALK(2p23)基因斷裂探針
EML4/ALK融合基因 t(2;2); inv(2) 探針
1p和19q探針
KIT(4q12)基因探針(紅色)
SS18(18q11)(SYT)基因斷裂探針
C-MET(7q31)基因探針
ROS1(6q22)基因斷裂探針
ERCC1(19q13)基因探針
hWAPL(10q23)基因探針
AR基因擴(kuò)增檢測(cè)探針
MDM4(1q32)基因探針
12號(hào)染色體計(jì)數(shù)探針(綠色)
CBFB/MYH11融合基因inv (16), t (16;16)探針
TCF3/ PBX1融合基因t (1;19)探針
ESR1(6q25)基因探針
FGFR1(8p11)基因探針
p53/RB1/ATM/CSP12/D13S25基因探針(獨(dú)立 )
p53/D13S319/RB1/1q21/IGH基因探針(獨(dú)立)
NUP98基因斷裂檢測(cè)探針
NTRK1(1q22-q23.1)基因斷裂探針
RET(10q11)基因斷裂探針
PIK3CA(3q26)基因探針
TFE3(Xp11.2)基因斷裂探針
FGFR1(8p11)基因斷裂探針
3號(hào)染色體計(jì)數(shù)探針(綠色)
7號(hào)染色體計(jì)數(shù)探針(綠色)
17號(hào)染色體計(jì)數(shù)探針(綠色)
10號(hào)染色體計(jì)數(shù)探針(綠色)
X染色體檢測(cè)探針
Y染色體計(jì)數(shù)探針(紅色)
13號(hào)染色體檢測(cè)探針
MLAA-34(13q14)基因探針


 


  

4691706572_1998788463

Over the past decades, researchers have found over 100 genes that may increase the risk of schizophrenia, which can lead to a serious mental disorder, which can lead to chaotic thinking, delusion and hallucination. One of these genes is called neuromodulation protein 3, which has a higher risk of schizophrenia. But until recently, researchers have not been able to determine how neuromodulation protein 3 affects the risk of schizophrenia.
Brain-153550__340
A new study has shown how a highly risky gene inhibits key brain chemicals.
In February 20, 2018 "published in the proceedings of the National Academy of Sciences" (Proceedings of the National Academy of Sciences) a new study in the journal, Cleveland (Cleveland) Western Reserve University (Case Western Reserve University) researchers found that neuregulin 3 and some neurotransmitters (chemical substances to help brain cells to communicate with each other the occurrence of chaos). They said that these findings may help to further develop a more targeted drug therapy for schizophrenia and other severe mental disorders in the future.
In the United States, 1 of the 100 people have schizophrenia, and the cause of schizophrenia is not yet clear. Doctors and scientists believe that the combination of genes and environmental factors is likely to play a role.
Dr. neuroscientist Lin Mei Ohio at Cleveland University School of medicine, said: "the treatment of severe mental illness is far from satisfactory. The brain is so complex that we have just begun to understand how different brain circuits and pathways interact to cause disease. "
This new study helps to reveal a potential pathway for the nerve to be affected: the neuroregulated protein 3 (also known as neuregulin 3). Dr. Mei and his colleagues know that some people with schizophrenia have increased the level of protein, but it is not clear what the level of this protein is related to the risk of schizophrenia.
Dna-163466__340
What is the link between genetics (gene) and mental illness?
Dr. Mei and his colleagues mutated the genes encoding the neuroregulatory protein 3 protein in different brain cell groups in mice. They want to prove which types of brain cells may be sensitive to changes in protein levels. When they are in pyramidal neurons (a special type of help to activate the brain's brain cells) in the mutant gene, they found that mice are difficult to navigate in the maze, and unfamiliar mice exhibiting strange behavior, researchers say these behaviors and schizophrenia is consistent.
Dr. Mei said schizophrenia is a mental disorder, and it is impossible to know what the mice are thinking. Mouse studies can help researchers identify the types of nerve cells that may be involved.
There is evidence that genes may interfere with the communication of brain cells.
The researchers then carefully studied the role of neuromodulation protein 3 at the cellular level. They cultured pyramidal neurons in Petri dishes of laboratory, and increased the level of neural regulatory protein 3 to simulate the protein levels found in the brains of schizophrenic patients.

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