i（17q）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，。

i（17q）探針

   本試劑盒主要用于i（17q）的檢測，17q等臂染色體是在腫瘤中zui常見的等臂染色體，預后極差。
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：

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】

每年2月的zui后一天是世界罕見病日。記者從廣東省醫學會罕見病學分會了解到，目前范圍內已確認的罕見病種占人類疾病的10%左右，總數有6000~7000種，多數是先天性因素引起的“疑難雜癥”。

廣州市婦女兒童醫療中心兒童內分泌科劉麗教授介紹，罕見病70%~80%能找到基因上的問題，表現多種多樣，有的是神經系統癥狀，有的是肝脾系統癥狀，頑固性貧血也可能是罕見病引起。如果是有家庭聚集性、診斷不明確、治療效果不明顯等“與眾不同”的病，就要警惕是罕見病的可能。

專家提醒，假如家有疑似患有罕見病的孩子想再生育一個健康的孩子，在再次生育前，首先應該明確診斷孩子患的是什么疾病，在備孕前接受遺傳咨詢，了解再次生育同樣疾病孩子的風險、是否適合再次生育。再次懷孕后，應該在懷孕15周以內及早進行產前診斷，看看胎兒是否患有同樣疾病并進行處理。對于自身患有罕見病，希望生個健康的寶寶的人群來說，同樣可以通過遺傳咨詢、產前診斷來中斷遺傳。

劉麗介紹，由于不同罕見病有多種癥狀，患者分散在不同科室，一般醫生每年碰到的某種罕見病患者非常有限，要讓所有相關醫生都熟練掌握各種罕見病的診斷、治療并不現實，如今省醫學會罕見病學分會正在組建罕見病醫聯體，由廣州市內部分大醫院及粵北、粵西、粵東等地市縣醫院組成，通過網絡對基層醫療接收到的疑難病例進行會診，遠程指導當地醫生為患者做相應檢查，將可疑病例轉到大醫院進行集中治療。在大醫院接受治療后病情穩定的患者，可以下轉回基層醫院，并由大醫院醫生通過網絡對當地醫生指導后續治療。

The last day of February is the rare day of the world. Reporters from the Guangdong Provincial Medical Association rare disease branch learned that rare diseases worldwide confirmed human diseases accounted for about 10%, the total number of 6000~7000, mostly caused by congenital factors Difficult miscellaneous diseases "".

Professor Liu Li, a child Department of endocrinology in Guangzhou women's and children's Medical Center, introduced rare diseases. 70%~80% can find genetic problems. There are various manifestations. Some are neurological symptoms. Some are symptoms of liver and spleen system. Refractory anemia may also be caused by rare diseases. If there is a family aggregation, the diagnosis is not clear, the treatment effect is not obvious and so on "different" disease, we should be alert to the possibility of rare diseases.

The expert reminds, if there are suspected of suffering from a rare disease of children want to give birth to a healthy child, again before birth, first of all should be clear what is the diagnosis of children suffering from disease, in the preparation of pregnancy received genetic counseling, again have the same disease risk, understand whether it is suitable for child birth again. After another pregnancy, it should be carried out early in the 15 weeks of pregnancy for prenatal diagnosis, to see if the fetus is suffering from the same disease and to be treated. Genetic counseling and prenatal diagnosis can also be used for people who have a rare disease and want to have a healthy baby.

Liu Li, due to a variety of different symptoms of rare diseases, patients scattered in different departments, general practitioners of a rare disease patients met every year is very limited, to all relevant doctors are skilled in diagnosis, all kinds of rare disease treatment is not realistic, now the Medical Association of rare diseases branch is the formation of rare disease conjoined by Guangzhou city hospital and divided northern and Western and eastern counties such as hospitals, through consultation of difficult cases received primary care network, remote guidance of local doctors do the corresponding examination for patients suspected cases will be transferred to a big hospital for centralized treatment. Patients with stable disease after receiving treatment in large hospitals can be transferred back to the basic level hospitals, and the doctors in large hospitals can guide the follow-up treatment for local doctors through the Internet.