- 產品描述
AML/ETO融合基因檢測試劑盒 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)是初治急性粒細胞白血病(AML)患者中常見的細胞遺傳學異常,大約20%~40%的AML-M2患者有t(8;21)(q22;q22),并且在M2b亞型中發生率高達90%以上。位于染色體21q22的AML1基因與8q22的ETO基因融合,產生AML1/ETO融合基因。AML1/ETO融合基因是轉錄激活基因,導致細胞不斷增殖。臨床上t(8;21)白血病好發于青年和兒童(5%~10%),主要與M2型密切相關,并且年齡越小發生率越高。t(8;21)代表預后較好的急性白血病類型,成人患者對治療反應佳,*緩解率高,中位生存時間長,但易復發;兒童患者的治療和預后不如成人患者理想。AML1/ETO融合基因可作為M2b診斷分型的標志,以及微小殘留病灶監測的一項檢測手段。
AML/ETO融合基因檢測試劑盒 熒光原位雜交法
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以下是我司出售的部分FISH產品:
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染色體計數探針 |
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基因擴增檢測探針 |
MDM4(1q32)基因探針 |
12號染色體計數探針(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(獨立 ) |
p53/D13S319/RB1/1q21/IGH基因探針(獨立) |
NUP98基因斷裂檢測探針 |
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號染色體計數探針(綠色) |
7號染色體計數探針(綠色) |
17號染色體計數探針(綠色) |
10號染色體計數探針(綠色) |
X染色體檢測探針 |
Y染色體計數探針(紅色) |
13號染色體檢測探針 |
MLAA-34(13q14)基因探針 |
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.