ATM（11q22）基因探针
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ATM（11q22）基因探针 本试剂盒主要用于ATM（11q22）基因的检测，里面包括即用型杂交液和DAPI复染剂。 本试剂盒仅供科研使用。
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ATM（11q22）基因探针
广州健仑生物科技?有限公司
本司长期供应尼古丁（可替宁）检测试剂盒，其主要品牌包括美国NovaBios、广州健仑、广州创仑等进口产品，国产产品，试剂盒的实验方法是胶体金方法。
我司还有很多荧光原位杂交系列检测试剂盒以及各种FISH基因探针和染色体探针等，。
ATM（11q22）基因探针
本试剂盒主要用于ATM（11q22）基因的检测，里面包括即用型杂交液和DAPI复染剂。
本试剂盒仅供科研使用。
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以下是我司出售的部分FISH产品：
| BCL6（3q37）基因断裂探针 |
| 13/18/21/XY染色体计数探针 |
| XY染色体计数探针 |
| p53/RB1/ATM/CSP12/D13S25基因探针 |
| 5q33/5q31/D7S486/D7S522/CSP8/D20S108/XY基因探针 |
| 4/10/17/KMT2A[ETV6RUNX1]/[BCRABL(DF)]基因探针 |
| p53/D13S319/RB1/1q21/IGH基因探针 |
| 13/16/18/21/22/XY染色体计数探针 |
| ALK（2p23）基因断裂探针 |
| EML4/ALK融合基因 t(2;2); inv(2) 探针 |
| 1p和19q探针 |
| KIT（4q12）基因探针（红色） |
| SS18（18q11）（SYT）基因断裂探针 |
| 乳腺癌染色体数目异常检测探针 |
| C-MET（7q31）基因探针 |
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【公司名称】 广州健仑生物科技有限公司
【】 杨永汉
【】
【腾讯 】
【公司地址】 广州清华科技园创新基地番禺石楼镇创启路63号二期2幢101-3室
【企业文化宣传】
今年的主题是“听见未来，从预防开始”，耳部疾病预防再度引发社会关注。一条有关儿童用药不当致聋的公益广告，也于近期在社交刷屏。统计显示，有类似遭遇的儿童，我国每年约有3万名之多。针对这一问题以及防范方法，北京晨报记者日前采访了相关专家。
专家表示，造成儿童耳聋的主要药物是氨基糖甙类药物。因此，儿童用药应格外谨慎，原则上不使用有明确耳毒性的氨基糖甙类药物。此外，儿童中存在药物性致聋基因携带者，一旦接触此类药物，极易致聋。通过耳聋基因检测，可尽早发现，避免药物性耳聋的发生。
药物性耳聋源自基因突变
在上面提到的公益广告中，一位5岁小朋友说道，自己因为3年前发高烧用药不当逐渐丧失听力。在以往的新闻报道中，也曾出现过儿童因为治疗感冒等常见病用药不当造成耳聋的案例。
据国家食药监总局南方医药经济研究所等发布的《2016年儿童用药安全调查报告baipi》显示，我国每年因用药不当约有3万名儿童耳聋。
对于因用药不当致聋的儿童在耳聋患者中的比例，北京电力医院耳科专业副主任医师赵亮进行了估算，他举例说，“1999年，上海对市属的4所聋哑学校共计275名学生进行调查，明确因药物导致耳聋的孩子占71%;其他地区的报道显示，药物性耳聋的比例也多在50%上下。我国有听力残疾的总人数约2780万，按照这个比例计算，药物性耳聋的儿童人群是相当庞大的。”
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.
