PDGFRB（5q32）基因断裂探针
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PDGFRB（5q32）基因断裂探针 本试剂盒主要用于PDGFRB（5q32）基因断裂的检测，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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PDGFRB（5q32）基因断裂探针
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，。
PDGFRB（5q32）基因断裂探针
本试剂盒主要用于PDGFRB（5q32）基因断裂的检测，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】
Have become fashionable for a time of ice bucket challenge, let the people know this rare disease amyotrophic lateral sclerosis. In fact, rare diseases are not rare. There are more than 7000 confirmed cases in the world, accounting for about 10% of the human disease.
February 28th is the world's rare disease day. CMT (Charcot Marie Tooth disease) care home, the family of care for the family of Bray disease, etc. recently launched a publicity campaign at the Hong Kong Shenzhen hospital, calling on the society to pay attention to rare diseases. The reporter has learned that most of the rare patients are faced with a difficult situation of diagnosis, no medical treatment, no medicine, no medicine.
Patients with rare diseases
The time of diagnosis is long
According to reports, a rare disease called "orphan", refers to the prevalence rate is very low, a rare disease, such as the "porcelain doll" "phenylketonuria" getting cold syndrome "mucopolysaccharide disease" and "Gaucher disease", mostly chronic and severe disease, often life-threatening. At present, 80% of the known rare diseases are hereditary diseases, which are caused by defective genes, and the diagnosis of most rare patients is a long process.
48 year old Huang is a Fabre disease, Fabre's disease is a rare X-linked hereditary X lysosomal storage diseases, age proteinuria, arrhythmia, vomiting, abdominal pain and diarrhea with, and then develop into kidney failure, heart failure. From outside, Mr. Huang did not have any difference from the normal person, and the condition was confirmed only a few years ago. "When I was 44 years old, I was diagnosed with French Bray disease. When I was younger, I had mild symptoms. Until I was nearly 40 years old, I found that my heart and kidneys had problems. I was diagnosed by kidney puncture and gene testing. Mr. Huang said.
The treatment of rare disease drug shortage
And the price is expensive
There is the biggest problem currently facing the domestic rare disease. At present, most rare diseases have no treatment in China, and foreign clinical trials are still being explored. The lack of drugs and the price of expensive drugs are also a heavy burden to the families of these rare patients.
