ATM（11q22）基因探針
| 型 號： | |
| 報 價： |  |
ATM（11q22）基因探針 本試劑盒主要用于ATM（11q22）基因的檢測，里面包括即用型雜交液和DAPI復染劑。 本試劑盒僅供科研使用。
- 產品描述
ATM（11q22）基因探針
廣州健侖生物科技?有限公司
本司長期供應尼古丁（可替寧）檢測試劑盒，其主要品牌包括美國NovaBios、廣州健侖、廣州創侖等進口產品，國產產品，試劑盒的實驗方法是膠體金方法。
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，。
ATM（11q22）基因探針
本試劑盒主要用于ATM（11q22）基因的檢測，里面包括即用型雜交液和DAPI復染劑。
本試劑盒僅供科研使用。
歡迎咨詢
歡迎咨詢
以下是我司出售的部分FISH產品：
| BCL6（3q37）基因斷裂探針 |
| 13/18/21/XY染色體計數探針 |
| XY染色體計數探針 |
| 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 |
| 乳腺癌染色體數目異常檢測探針 |
| C-MET（7q31）基因探針 |
二維碼掃一掃
【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】 廣州清華科技園創新基地番禺石樓鎮創啟路63號二期2幢101-3室
【企業文化宣傳】
今年的主題是“聽見未來，從預防開始”，耳部疾病預防再度引發社會關注。一條有關兒童用藥不當致聾的公益廣告，也于近期在社交刷屏。統計顯示，有類似遭遇的兒童，我國每年約有3萬名之多。針對這一問題以及防范方法，北京晨報記者日前采訪了相關專家。
專家表示，造成兒童耳聾的主要藥物是氨基糖甙類藥物。因此，兒童用藥應格外謹慎，原則上不使用有明確耳毒性的氨基糖甙類藥物。此外，兒童中存在藥物性致聾基因攜帶者，一旦接觸此類藥物，極易致聾。通過耳聾基因檢測，可盡早發現，避免藥物性耳聾的發生。
藥物性耳聾源自基因突變
在上面提到的公益廣告中，一位5歲小朋友說道，自己因為3年前發高燒用藥不當逐漸喪失聽力。在以往的新聞報道中，也曾出現過兒童因為治療感冒等常見病用藥不當造成耳聾的案例。
據國家食藥監總局南方醫藥經濟研究所等發布的《2016年兒童用藥安全調查報告baipi》顯示，我國每年因用藥不當約有3萬名兒童耳聾。
對于因用藥不當致聾的兒童在耳聾患者中的比例，北京電力醫院耳科專業副主任醫師趙亮進行了估算，他舉例說，“1999年，上海對市屬的4所聾啞學校共計275名學生進行調查，明確因藥物導致耳聾的孩子占71%;其他地區的報道顯示，藥物性耳聾的比例也多在50%上下。我國有聽力殘疾的總人數約2780萬，按照這個比例計算，藥物性耳聾的兒童人群是相當龐大的。”
The theme of this year is "hearing the future, starting from the prevention", and the prevention of the ear disease has reigned the social concern again. A children's hearing loss caused by improper use of public service ads, also recently on the social networking site shuabing. Statistics show that there are about 30 thousand children in our country each year. To solve this problem and prevent method, the Beijing morning news reporters recently interviewed the experts.
Experts said that the main cause of deafness is children's drug aminoglycosides. Therefore, children should be extra cautious, in principle, without the use of aminoglycoside ototoxicity is clear. In addition, drug-induced deafness gene carriers exist in children, once exposed to these drugs, very prone to cause deafness. Through the detection of the deafness gene, it can be found as soon as possible to avoid the occurrence of drug deafness.
From drug deafness gene mutation
Public service advertising mentioned above, a 5 year old friend said, because 3 years ago, high fever, inappropriate medication gradually lose hearing. In the past news reports, there have also been cases of deafness caused by children's improper use of common diseases such as colds.
According to the State Food and Drug Administration Southern Medicine Economic Research Institute released the "survey of child safety medication in 2016 white paper" shows that in our country due to improper medication about 30 thousand children a year deafness.
For improper use of deaf children in deaf patients in proportion, deputy director of Beijing Electric Power Hospital physician Zhao Liang ear were estimated, for example, in 1999, Shanghai conducted a survey of 4 Municipal School for the deaf students from 275, clear for drug induced deafness children accounted for 71%; in other areas according to reports, the proportion of drug deafness in more than 50%. The total number of hearing disabled people in our country is about 27 million 800 thousand. According to this proportion, the population of children with drug-induced deafness is quite large.
