91免费视频网址丨日韩一区在线视频丨亚洲色欲久久久久综合网丨日本少妇自慰免费完整版丨国产日韩精品一区二区三区在线丨图片小说视频一区二区丨成年男女免费视频网站丨视频在线不卡丨日韩精品高清在线丨97视频在线免费观看丨日韩精品人妻中文字幕有码丨性欧美老妇另类xxxx丨久艹在线视频丨国产寡妇xxxxxxxx性开放丨欧美人与牲动xxxx丨欧美成人在线视频丨人妻在线无码一区二区三区丨精品无码国产一区二区三区av丨国产好片无限资源丨午夜三级a三级三点窝

Clinical Application

Alpha thalassemia (α-thalassemia) is a kind of monogenic inheritance hemopathy due to expression imbalance of peptide chain caused by alpha-globin gene mutation. It is one of the most common and most harmful inherited diseases in various provinces in the south of China. The common alpha-globin gene mutation types among Chinese are mainly three deletion types of -α^3.7, -α^4.2  and --^SEA . In addition, there was one of the deletion type α-thalassemia has also been reported in China, --^THAI .

Intended Use

This kit is used for in vitro qualitative detection of whether human whole blood DNA sample is with alpha thalassemia deleted gene, which can detect four kinds of deletion types of alpha thalassemia SEA THAI (-α3.7 , -α4.2 , -- SEA, --THAI ) simultaneously.

Packing Specifications

General Specification

Methodology: Real-Time PCR, PCR- Multicolor Melting Curve
Sample Type: anti-coagulation whole blood
Precision: CV <1%
LoD: 0.5 ng/&mu;L