更短的时间！ 15分钟内获得纯净的DNA!
更快的操作！无需蛋白酶K消化去除红细胞！
更高的回收率！可直接从400 µl全血中分离纯化到5-20 µg 高纯度基因组DNA

实验室操作产品对比：

品牌	试剂盒名称	操作时间	标本最大体积	货号
Simgen	全血DNA小量试剂盒	7分钟	400 µl	3001050
Qiagen	QIAamp DNA Blood Mini Kit	17分钟	200µl	51104
国产（TG）	血液基因组DNA提取试剂盒	21分钟 (不含裂解红细胞步骤)	200µl 超过200µl需要用红细胞裂解液去除红细胞	DP348
Omega	E.Z.N.A Blood DNA Kit	28分钟	250µl	D3392
Axygen	AxyPrep血基因组DNA小量试剂盒	18分钟	250µl	AP-MN-BL-GDNA

提取效果展示：

图为6人血样用全血DNA小量试剂盒提取的基因组效果图，孔1为1kb ladder Marker，孔2-7为所提取的基因组DNA。

真实用户体验反馈：
浙二医院用户的评价：比Qiagen的产品更好用！
宁波大学老师评价：比TG和KWSJ的速度更快，得率更高，纯度更好！
* 15分钟内从400 µl全血中分离纯化到5-15 µg 高纯度基因组DNA（OD₂₆₀/OD₂₈₀=1.7-1.9）!
* 不需要蛋白酶K消化，不需要水浴锅，仅需一台台式小量离心机即可操作！
* 适用于新鲜的抗凝血、冷冻后溶血的抗凝血、甚至是含有少量血凝块的抗凝血！
* 大批量血样中分离纯化DNA的最佳选择！
大批忠实粉：
浙江大学医学院
浙江大学医学院附属第一医院
浙江大学医学院附属第二医院
杭州迪安医学检验中心
杭州博泰基因技术有限公司
吉林大学第一医院
泰普生物技术（中国）有限公司
亚能生物技术（深圳）有限公司
珠海赛乐奇生物技术有限公司

文献收集（持续更新中）：
（进入google学术搜索，键入“simgen kit”即可获得大量文献）
1. A novel p. R890C mutation in EPHA2 gene associated with progressive childhood posterior cataract in a Chinese family
XC Shentu, SJ Zhao, L Zhang… - International journal of …, 2013 - ncbi.nlm.nih.gov
2. The TGFBI R555W mutation induces a new granular corneal dystrophy type I phenotype
Y Zhu, X Shentu, W Wang - Molecular vision, 2011 - ncbi.nlm.nih.gov
3. Molecular diagnosis of a Chinese pedigree with α-mannosidosis and identification of a novel missense mutation
X Wu, J Pan, Y Guo, C Guo, W Jiang, R Li… - Journal of Pediatric …, 2014 - degruyter.com
4. A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family
Y Yu, Y Yu, P Chen, J Li, Y Zhu, Y Zhai… - BMC medical …, 2014 - biomedcentral.com
5. Novel mutation c. 980_983delATTA compound with c. 986C> A mutation of the FRMD7 gene in a Chinese family with X-linked idiopathic congenital nystagmus
F Song, B Chen, Z Sun, L Wu, S Zhao, Q Miao… - Journal of Zhejiang …, 2013 - Springer
6. Chinese family with atypical granular corneal dystrophy type I caused by the typical R555W mutation in TGFBI
SJ Zhao, YN Zhu, XC Shentu, Q Miao - International journal of …, 2013 - ncbi.nlm.nih.gov
7. Molecular analysis and phenotypic study in 14 Chinese families with Bietti crystalline dystrophy
H Yin, C Jin, X Fang, Q Miao, Y Zhao, Z Chen, Z Su… - PloS one, 2014 - dx.plos.org
8. Identification and Functional Analysis of a Novel MIP Gene Mutation Associated with Congenital Cataract in a Chinese Family
X Shentu, Q Miao, X Tang, H Yin, Y Zhao - 2015 - dx.plos.org
9. Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome
H Yin, X Fang, C Jin, J Yin, J Li, S Zhao, Q Miao… - Journal of Zhejiang …, 2014 - Springer
10. Molecular analysis of SLC25A13 gene in human peripheral blood lymphocytes: Marked transcript diversity, and the feasibility of cDNA cloning as a diagnostic tool for …
ZH Zhang, WX Lin, M Deng, XJ Zhao, YZ Song - Gene, 2012 - Elsevier
11.Characterization of the Relationship between APOBEC3B Deletion and ACE Alu Insertion
K Wang, Y Li, C Dai, K Wang, J Yu, Y Tan, W Zhang… - 2013 - dx.plos.org
12. CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patients
Y Wang, XF Huang, MM Yang, WJ Cai… - British Journal of …, 2014 - bjo.bmj.com
13. Association of fetal but not maternal P-glycoprotein C3435T polymorphism with fetal growth and birth weight, a possible risk factor for cardiovascular diseases in …
J Li, ZN Wang, YP Chen, YP Dong, XM Xiao… - Clinical …, 2012 - uni-potsdam.de
14. A functional fetal HSD11B2 [CA] n microsatellite polymorphism is associated with maternal serum cortisol concentrations in pregnant women
J Li, YP Chen, ZN Wang, TB Liu, D Chen… - Kidney and Blood …, 2013 - karger.com
15. A missense mutation in the arginine‐vasopressin neurophysin‐II gene causes autosomal dominant neurohypophyseal diabetes insipidus in a Chinese family
D Ye, FQ Dong, WQ Lu, Z Zhang, XL Lu… - Clinical …, 2013 - Wiley Online Library
16. Association of CD40-1C/T Polymorphism in the 5′-Untranslated Region with Chronic HBV Infection
C Zhou, X Jin, J Tang, J Fei, C Gu… - Cellular Physiology and …, 2015 - karger.com
17. A novel phenotype-genotype correlation with an Arg555Trp mutation of TGFBI gene in Thiel-Behnke corneal dystrophy in a Chinese pedigree
Y Yu, P Qiu, Y Zhu, J Li, M Wu, B Zhang… - BMC …, 2015 - biomedcentral.com
18. Zhu Y, Shentu X, Wang W, et al. A Chinese family with progressive childhood cataracts and IVS3+ 1G> A CRYBA3/A1 mutations[J]. Molecular vision, 2010, 16: 2347. 影响因子：1.986
19. ABCB1 基因多态性与母胎界面糖皮质激素的转运关系
李健， 王自能 - 暨南大学学报(自然科学与医学版), 2011 - jnxb.jnu.edu.cn
20. Citrin缺陷病致病基因SLC25A13高频突变筛查试剂盒
宋元宗，张占会
21. Citrin缺陷导致的新生儿肝内胆汁淤积症患儿SLC25A13基因突变与生化指标的相关性研究
22. 藏酋猴Mhc-DPB1 基因exon 2 的多态性
李佳薏， 姚永芳， 周亮， 徐怀亮 - 遗传, 2012 - chinagene.cn
23. 四川地区猕猴线粒体DNA 控制区遗传多样性及其种群遗传结构
徐怀亮， 李地艳， 程安春， 姚永芳， 倪庆永， 曾文… - 兽类学报, 2010 - mammal.cn