昆蟲基因組DNA提取試劑盒
Insect
Genomic DNA Isolation Kit
● 試劑盒内容及保存:
試劑盒組成
|
RTG2408
(50次)
|
貯存方式
|
緩沖液IL
|
22
ml
|
常溫
|
緩沖液IB(濃縮液)
|
26
ml
|
常溫
|
DNA
Wash Buffer (濃縮液)
|
65
ml
|
常溫
|
緩沖液WB(濃縮液)
|
30
ml
|
常溫
|
洗脫緩沖液EB
|
15
ml
|
常溫
|
蛋白(bái)酶K
|
1.05
ml
|
-20℃
|
RNaseA
|
220
μl
|
-20℃
|
吸附柱CG(含收集管)
|
50套
|
常溫
|
|
|
|
說明書
|
1份
|
|
● 儲存條件(jiàn)和效期:
室溫保存,12個(gè)月(yuè)内有效。緩沖液IL與緩沖液 IB可能(néng)有沉澱産生(shēng),37℃水(shuǐ)浴溶解後即可。RNase
A和蛋白(bái)酶K常溫運輸,-20℃保存。
● 産品簡介:
該試劑盒采用獨特的裂解液能(néng)夠有效除去多(duō)糖多(duō)酚等,能(néng)夠從(cóng)昆蟲、軟體動物(wù)、節肢動物(wù)、蛔蟲等樣品中提取DNA,保存在醇類的樣品也适用于本試劑盒的提取。一(yī)次操作可以處理小(xiǎo)于50mg組織,樣品經裂解液消化,氯仿分離除去大部分的多(duō)糖多(duō)酚,再經分離柱進一(yī)步純化,便可得到(dào)高(gāo)純度的DNA。所得的DNA可以用于PCR,Southern雜(zá)交,酶切消化等實驗。
● 準備工(gōng)作:
1. 準備65℃水(shuǐ)浴;無水(shuǐ)乙醇;氯仿;制冰機(jī);1.5ml離心管;2ml離心管
2. 按照(zhào)标簽所示在緩沖液IB中加入異丙醇,在DNA Wash Buffer和緩沖液WB中加入無水(shuǐ)乙醇,混勻後蓋緊瓶蓋後常溫貯存備用。
3. 每次使用前請檢查緩沖液IL,緩沖液IB是否有沉澱生(shēng)成,如果出現沉澱,37℃溫浴至沉澱溶解後再使用。
● 标準操作步驟:
如非指出,所有離心步驟均為(wèi)使用台式離心機(jī)在常溫下(xià)離心。
1. 液氮充分研磨樣品。
2. 收集研磨成粉末的50
mg樣品,置于1.5ml離心管中。
3. 加入350 μl65℃預熱的緩沖液 IL,并加入20μl 蛋白(bái)酶K劇烈地漩渦振蕩,确保所有的組織團都分散均勻。
4.65℃水(shuǐ)浴20-30min。水(shuǐ)浴期間颠倒樣品數次。
5. 加入350 μl氯仿,充分混勻,12,000 rpm (~13,400×g )
離心5分鍾。
6. 小(xiǎo)心地把上(shàng)清液吸至另一(yī)新的1.5ml離心管中。注意确保不要打散沉澱團或把組織碎片也一(yī)起轉移。
7. 加入4 μl
RNase A,渦旋混勻。常溫放(fàng)置2min。
8. 加入等體積的緩沖液
IB(請确保已經按照(zhào)标簽加入異丙醇),充分混勻。如:向300μl上(shàng)清中加入300 μl 緩沖液 IB。
9. 把上(shàng)述混勻的液體轉移到(dào)吸附柱CG上(shàng)。10,000×g離心1
min以結合DNA,棄去濾出液體。純化柱最大容量為(wèi)750 μl,如果混合液大于750 μl,請分兩次過柱。
10. 将吸附柱重新套回收集管中,加入500μl
緩沖液WB(請确保已經按照(zhào)标簽加入無水(shuǐ)乙醇)至柱子中,10,000×g離心1min,倒棄流出液;
11. 将吸附柱重新套回收集管中,加入600μl
DNA Wash Buffer(請确保已經按照(zhào)标簽加入無水(shuǐ)乙醇)至柱子中,10,000×g離心1min,倒棄流出液;
注意:DNA Wash Buffer使用前須按要求用無水(shuǐ)乙醇稀釋。如果放(fàng)入冰箱中,使用前須恢複到(dào)室溫。
12.再加入600μl
DNA Wash Buffer(請确保已經按照(zhào)标簽加入無水(shuǐ)乙醇)至柱子中,8,000×g離心1min,棄去流出液;
13. 将吸附柱重新套回2ml收集管中,最大轉速(>13000×g)離心空結合柱1min以幹燥柱子的基質;這一(yī)步對下(xià)面的洗脫步驟至關重要。
14. 将柱子置于1.5
ml滅菌離心管,加入50-150 μl 65℃預熱的洗脫緩沖液EB至柱子的膜中央。常溫靜(jìng)置5 min;
15. 常溫下(xià),離心(>13000g)1min,以洗脫DNA。保留含DNA的流出液。将DNA儲于-20℃。
● DNA濃度及純度檢測:
基因組DNA片段的大小(xiǎo)與樣品保存時間、操作過程中的剪切力等因素有關。提取的DNA片段可用瓊脂糖凝膠電(diàn)泳和紫外分光(guāng)光(guāng)度計檢測濃度與純度。可配制0.8-1.0%瓊脂糖凝膠,使用λ/HindIII判斷基因組的大小(xiǎo),完整的基因組大小(xiǎo)應在23kb以上(shàng)。使用分光(guāng)光(guāng)度計檢測時, OD260/OD280比值應為(wèi)1.7–1.9之間,如果洗脫時不使用洗脫緩沖液,而使用去離子水(shuǐ)洗脫,比值可能(néng)偏低(dī),但并不表明DNA純度不高(gāo)。
常見(jiàn)問題
|
可能(néng)原因
|
建議
|
堵柱子
|
轉移裂解上(shàng)清時,轉移了沉澱
|
按說明書操作,氯仿分離後,确保不轉移到(dào)沉澱
|
樣品太粘稠
|
樣品量别超過說明書上(shàng)所說的,或者增加緩沖液IB的用量。
|
低(dī)濃度的DNA量
|
樣品的破壁方式不對
|
不論新鮮還(hái)是幹燥樣品,在加入緩沖液IL之前必須用适當方式的研磨成粉末。
|
樣品的裂解效果不好
|
減少樣品量,或者增加緩沖液IL的用量。
|
DNA殘留在柱子上(shàng)
|
增加洗脫液EB的用量,并在離心洗脫前将洗脫液EB65℃孵育5min。
|
DNA洗滌不當
|
DNA
Wash Buffer按說明書用無水(shuǐ)乙醇稀釋。
|
下(xià)遊應用不好
|
提取的DNA含鹽量高(gāo)
|
DNA
Wash Buffer必須按要求用無水(shuǐ)乙醇稀釋,必須常溫放(fàng)置。
|
提取的DNA含有乙醇
|
洗脫前,必須最高(gāo)轉速空甩柱子1min。
|
核酸提取産品發表文章
1. [2008 IF=1.749] Development of a sequence-characterized
ampli?ed region marker for diagnosis of dwarf bunt of wheat and detection of
Tilletia controversa Kuhn.
Author: J.H. Liu, L. Gao, T.G. Liu and W.Q. Chen
Product: RTP2201 瓊脂糖凝膠回收試劑盒
Journal: Letters in Applied Microbiology 2009,49,235-240
Institution:Institute of
Plant Protection ,Chinese Academy of Agricultural Sciences
Paper link: https://doi.org/10.1111/j.1472-765X.2009.02645.x
2. [2009 IF=2.435] Characterization of three new S-alleles
and development of an S-allele-specific PCR system for rapidly identifying the
S-genotype in apple cultivars.
Author: Shenshan Long, Maofu Li, Zhenhai Han, Kun Wang, Tianzhong Li
Product: RTP2201瓊脂糖凝膠回收試劑盒
Journal: Tree Genetics & Genomes (2010)
6:161–168
Institution:China
Agricultural University
Paper link: https://link.springer.com/article/10.1007/s11295-009-0237-6
3. [2010 IF=0.921] An ISSR-based Approach for the Molecular
Detection and Diagnosis of Dwarf Bunt of Wheat, Caused by Tilletia controversa
Kuhn.
Author: Li Gao,Wanquan Chen and Taiguo Liu
Product: RTP2201 瓊脂糖凝膠回收試劑盒
Journal: J Phytopathol 159:155–158 (2011)
Institution:State Key
Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant
Protection, CAAS
Paper link:https://onlinelibrary.wiley.com/doi/10.1111/j.1439-0434.2010.01735.x
4. [2010 IF=1.359] Curing the Plasmid pXO2 from Bacillus
anthracis A16 Using Plasmid Incompatibility.
Author: Huagui Wang, Xiankai Liu, Erling Feng, Li Zhu, Dongshu Wang, Xiangru Liao,
Hengliang Wang
Product: RTP2201 瓊脂糖凝膠回收試劑盒
Journal: Curr Microbiol (2011) 62:703–709
Institution:State Key
Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology
Paper link:https://link.springer.com/article/10.1007/s00284-010-9767-2
5. [2010 IF=1.993] Computation-assisted SiteFinding-PCR for
isolating flanking sequence tags in rice
Author: Hongru Wang, Jun Fang, Chengzheng Liang, Minghui He, Qiye Li, and
Chengcai Chu
Product: RTP2201 瓊脂糖凝膠回收試劑盒
Journal: BioTechniques Vol. 51 | No. 6 | 2011
Institution:Institute of
Genetics and Developmental Biology, Chinese Academy of Sciences
Paper link:https://pubmed.ncbi.nlm.nih.gov/22150334/
6. [2012 IF=0.903] T Polymorphisms in major
histocompatibility complex class IIa genes are associated with resistance to
infectious hematopoietic necrosis in rainbow trout, Oncorhynchus mykiss
(Walbaum, 1792).
Author: Z. Liu, D.-D. Hu, S.-J. Shao, J.-Q. Huang, J.-F. Wang and J. Yang
Product: RTP2202 PCR産物(wù)純化試劑盒
Journal: J. Appl. Ichthyol. 29 (2013), 1234–1240
Institution:College of
Animal Science and Technology, Gansu Agricultural University
Paper link:https://onlinelibrary.wiley.com/doi/full/10.1111/jai.12326
7. [2012 IF=1.958] Cloning, bioinformatics and the enzyme
activity analyses of a phenylalanine ammonia-lyase gene involved in dragon’s blood biosynthesis in Dracaena
cambodiana.
Author: Xing-Hong Wang,Changhe Zhang
Product: RTP2202 PCR産物(wù)純化試劑盒
Journal: Mol Biol Rep (2013) 40:97–107
Institution:Yunnan Institute
of Microbiology, Yunnan University
Paper link:https://link.springer.com/article/10.1007/s11033-012-2032-y
8. [2013 IF=1.687] Tobacco Arabinogalactan Protein NtEPc Can
Promote Banana (Musa AAA) Somatic Embryogenesis.
Author: H. Shu & L. Xu & Z. Li & J. Li & Z. Jin & S. Chang
Product: RTP2201 瓊脂糖凝膠回收試劑盒
Journal: Appl Biochem Biotechnol (2014)
174:2818–2826
Institution:Haikou
Experimental Station, Chinese Academy of Tropical Agricultural Sciences
Paper link:https://link.springer.com/article/10.1007/s12010-014-1228-0
9. [2015 IF=1.32] Association between MHC II beta chain gene
polymorphisms and resistance to infectious haematopoietic necrosis virus in
rainbow trout (Oncorhynchus mykiss, Walbaum, 1792).
Author: Juan Yang, Zhe Liu, Hai-Na Shi, Jiu-Pan Zhang, Jian-Fu Wang, Jin-Qiang
Huang & Yu-Jun Kang
Product: RTP2202 PCR産物(wù)純化試劑盒
Journal: Aquaculture Research, 2016, 47,
570–578
Institution:College of
Animal Science and Technology, Gansu Agricultural University
Paper link: https://onlinelibrary.wiley.com/doi/10.1111/are.12516
10. [2015 IF=] A weird DNA band in PCR and its cause.
Author: Chang Shenghe, Sun Wei, Zhou Zhaoxi, Li Jingyang, Dai Minjie, Shu Haiyan
Product: RTP2102 普通(tōng)質粒小(xiǎo)提試劑盒
Journal: Journal of Plant Science & Molecular
Breeding Volume 5 Article 2 2016
Institution:Haikou
experimental station, Chinese Academy of Tropical Agricultural Sciences
Paper link:
11. [2017 IF=4.076] Application of Real-Time Quantitative PCR
to Detect Mink Circovirus in Naturally and Experimentally Infected Minks.
Author: Xingyang Cui, Yunjia Shi, Lili Zhao, Shanshan Gu, Chengwei Wei, Yan
Yang,Shanshan Wen, Hongyan Chen and Junwei Ge
Product: RTP2102 普通(tōng)質粒小(xiǎo)提試劑盒
Journal: Fronties in Microbiology May 2018 | Volume 9 | Article 937
Institution:College of
Veterinary Medicine, Northeast Agricultural University
Paper link:https://pubmed.ncbi.nlm.nih.gov/29867846
12. [2017 IF=3.974] In vitro and in vivo toxic e?ects and in?ammatory responses induced by carboxylated
black carbon-lead complex exposure.
Author: Shuanglin Jiang,, Mengting Shang,Kui Mu,Nan Jiang,Haiyan Wen,Rong Wang,Hai Wu,Wenyong Li
Product: RTG2402 動物(wù)/細胞基因組DNA提取試劑盒
Journal: Ecotoxicology and Environmental
Safety 165 (2018)
484–494
Institution:Key Laboratory
of Embryo Development and Reproductive Regulation of Anhui Province, Fuyang
Normal University
Paper link:http://www.sciencedirect.com/science/article/pii/S0147651318309011
13. [2018 IF=8.063] ATF4 destabilizes RET through nonclassical
GRP78 inhibition to enhance chemosensitivity to bortezomib in human
osteosarcoma
Author: Jie Luo,# Yuanzheng Xia,# Yong Yin, Jun Luo, Mingming Liu, Hao Zhang,
Chao Zhang, Yucheng Zhao, Lei Yang, and Lingyi Kong
Product: RTP2101 高(gāo)純質粒小(xiǎo)提試劑盒
Journal: Theranostics 2019, Vol. 9, Issue 21
Institution:School of
Traditional Chinese Pharmacy, China Pharmaceutical University
Paper link:https://pubmed.ncbi.nlm.nih.gov/31534554
14. [2020 IF=1.857] Characterization and Developmental
Expression Patterns of Four Hexamerin Genes in the Bumble Bee, Bombus
terrestris (Hymenoptera: Apidae).
Author: Yakai Tian, Yingping Qu,Kun Dong,Shaoyu He,Wu Jie, and Jiaxing Huang
Product: RTP2201 瓊脂糖凝膠回收試劑盒
Journal: Journal of Insect Science (2021) 21(5): 13; 1–8
Institution:Institute of
Apicultural Research, Chinese Academy of Agricultural Sciences
Paper link:https://doi.org/10.1093/jisesa/ieab078
15. [2020 IF=1.336] Isopentenyl Diphosphate Isomerase (IPI)
Gene Silencing Negatively Afects Patchouli Alcohol Biosynthesis
in Pogostemon cablin
Author: Wuping Yan, Yuzhang Yang, Yougen Wu, Jing Yu, Junfeng Zhang,
Dongmei Yang, Zeeshan Ul Haq Muhammad
Product: RTP2102 普通(tōng)質粒小(xiǎo)提試劑盒
Journal: Plant Molecular Biology Reporter Published 27 January 2021
Institution:College
of Horticulture, Hainan University
Paper link:https://link.springer.com/article/10.1007/s11105-020-01269-0
16. [2021 IF=6.064] Genome resequencing and transcriptome
analysis reveal the molecular mechanism of albinism in Cordyceps militaris.
Author: Ying Zhao, YuDong Liu, Xun Chen and Jun
Xiao
Product: RTG2407 真菌基因組DNA提取試劑盒
Journal: Fronties in
Microbiology. Published 11 April 2023
Institution: Institute of Edible Fungi, Liaoning
Academy of Agricultural Sciences
Paper link:https://www.frontiersin.org/articles/10.3389/fmicb.2023.1153153/full