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首頁 > 核酸生(shēng)物學 > 核酸提取 > 基因組提取

昆蟲基因組DNA提取試劑盒

昆蟲基因組DNA提取試劑盒

産品編号:RTG2408

産品規格:50次

數量
價格 ¥700


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

常溫




說(shuō)明書(shū)

1

 

儲存條件(jiàn)和效期:

室溫保存,12個月内有效。緩沖液IL與緩沖液 IB可(kě)能有沉澱産生(shēng),37℃水浴溶解後即可(kě)。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夠有效除去(qù)多糖多酚等,能夠從(cóng)昆蟲、軟體(tǐ)動物、節肢動物、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。一次操作(zuò)可(kě)以處理(lǐ)小于50mg組織,樣品經裂解液消化,氯仿分(fēn)離(lí)除去(qù)大(dà)部分(fēn)的多糖多酚,再經分(fēn)離(lí)柱進一步純化,便可(kě)得(de)到高純度的DNA。所得(de)的DNA可(kě)以用于PCR,Southern雜交,酶切消化等實驗。

準備工(gōng)作(zuò):

1. 準備65℃水浴;無水乙醇;氯仿;制冰機(jī);1.5ml離(lí)心管;2ml離(lí)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中加入無水乙醇,混勻後蓋緊瓶蓋後常溫貯存備用。

3. 每次使用前請(qǐng)檢查緩沖液IL,緩沖液IB是否有沉澱生(shēng)成,如(rú)果出現沉澱,37℃溫浴至沉澱溶解後再使用。

标準操作(zuò)步驟:

如(rú)非指出,所有離(lí)心步驟均爲使用台式離(lí)心機(jī)在常溫下離(lí)心。

1. 液氮充分(fēn)研磨樣品。

2. 收集研磨成粉末的50 mg樣品,置于1.5ml離(lí)心管中。

3. 加入350 μl65℃預熱(rè)的緩沖液 IL,并加入20μl 蛋白(bái)酶K劇(jù)烈地漩渦振蕩,确保所有的組織團都(dōu)分(fēn)散均勻。

4.65℃水浴20-30min。水浴期間颠倒樣品數次。

5. 加入350 μl氯仿,充分(fēn)混勻,12,000 rpm (~13,400×g )  離(lí)心5分(fēn)鍾。

6. 小心地把上清液吸至另一新的1.5ml離(lí)心管中。注意确保不要打散沉澱團或把組織碎片也一起轉移。 

7. 加入4 μl RNase A,渦旋混勻。常溫放(fàng)置2min。

8. 加入等體(tǐ)積的緩沖液 IB(請(qǐng)确保已經按照(zhào)标簽加入異丙醇),充分(fēn)混勻。如(rú):向300μl上清中加入300 μl 緩沖液 IB。  

9. 把上述混勻的液體(tǐ)轉移到吸附柱CG上。10,000×g離(lí)心1 min以結合DNA,棄去(qù)濾出液體(tǐ)。純化柱最大(dà)容量爲750 μl,如(rú)果混合液大(dà)于750 μl,請(qǐng)分(fēn)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(qǐng)确保已經按照(zhào)标簽加入無水乙醇)至柱子中,10,000×g離(lí)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(qǐng)确保已經按照(zhào)标簽加入無水乙醇)至柱子中,10,000×g離(lí)心1min,倒棄流出液;

注意:DNA Wash Buffer使用前須按要求用無水乙醇稀釋。如(rú)果放(fàng)入冰箱中,使用前須恢複到室溫。 

12.再加入600μl DNA Wash Buffer(請(qǐng)确保已經按照(zhào)标簽加入無水乙醇)至柱子中,8,000×g離(lí)心1min,棄去(qù)流出液;

13. 将吸附柱重新套回2ml收集管中,最大(dà)轉速(>13000×g)離(lí)心空結合柱1min以幹燥柱子的基質;這一步對下面的洗脫步驟至關重要。 

14. 将柱子置于1.5 ml滅菌離(lí)心管,加入50-150 μl  65℃預熱(rè)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,離(lí)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(dà)小與樣品保存時間、操作(zuò)過程中的剪切力等因素有關。提取的DNA片段可(kě)用瓊脂糖凝膠電泳和紫外分(fēn)光(guāng)光(guāng)度計(jì)檢測濃度與純度。可(kě)配制0.8-1.0%瓊脂糖凝膠,使用λ/HindIII判斷基因組的大(dà)小,完整的基因組大(dà)小應在23kb以上。使用分(fēn)光(guāng)光(guāng)度計(jì)檢測時, OD260/OD280比值應爲1.7–1.9之間,如(rú)果洗脫時不使用洗脫緩沖液,而使用去(qù)離(lí)子水洗脫,比值可(kě)能偏低,但(dàn)并不表明DNA純度不高。

 

常見(jiàn)問(wèn)題

可(kě)能原因

建議(yì)

堵柱子

轉移裂解上清時,轉移了沉澱

按說(shuō)明書(shū)操作(zuò),氯仿分(fēn)離(lí)後,确保不轉移到沉澱

樣品太粘稠

樣品量别超過說(shuō)明書(shū)上所說(shuō)的,或者增加緩沖液IB的用量。

低濃度的DNA

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

增加洗脫液EB的用量,并在離(lí)心洗脫前将洗脫液EB65孵育5min

DNA洗滌不當

DNA Wash Buffer按說(shuō)明書(shū)用無水乙醇稀釋。

下遊應用不好

提取的DNA含鹽量高

DNA Wash Buffer必須按要求用無水乙醇稀釋,必須常溫放(fàng)置。

提取的DNA含有乙醇

洗脫前,必須最高轉速空甩柱子1min

 


核酸提取産品發表文章(zhāng)

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

InstitutionInstitute 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

InstitutionChina 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)

InstitutionState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, CAAS

Paper linkhttps://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

InstitutionState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology

Paper linkhttps://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

InstitutionInstitute of Genetics and Developmental Biology, Chinese Academy of Sciences

Paper linkhttps://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産物純化試劑盒

Journal: J. Appl. Ichthyol. 29 (2013), 1234–1240

InstitutionCollege of Animal Science and Technology, Gansu Agricultural University

Paper linkhttps://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産物純化試劑盒

Journal: Mol Biol Rep (2013) 40:97–107

InstitutionYunnan Institute of Microbiology, Yunnan University

Paper linkhttps://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

InstitutionHaikou Experimental Station, Chinese Academy of Tropical Agricultural Sciences

Paper linkhttps://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産物純化試劑盒

Journal: Aquaculture Research, 2016, 47, 570–578

InstitutionCollege 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 普通質粒小提試劑盒

Journal: Journal of Plant Science & Molecular Breeding  Volume 5 Article 2 2016

InstitutionHaikou 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 普通質粒小提試劑盒

Journal: Fronties in Microbiology May 2018 | Volume 9 | Article 937

InstitutionCollege of Veterinary Medicine, Northeast Agricultural University

Paper linkhttps://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/細胞基因組DNA提取試劑盒

Journal: Ecotoxicology and Environmental Safety 165 (2018) 484–494

InstitutionKey Laboratory of Embryo Development and Reproductive Regulation of Anhui Province, Fuyang Normal University

Paper linkhttp://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 高純質粒小提試劑盒

Journal: Theranostics 2019, Vol. 9, Issue 21

InstitutionSchool of Traditional Chinese Pharmacy, China Pharmaceutical University

Paper linkhttps://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

InstitutionInstitute of Apicultural Research, Chinese Academy of Agricultural Sciences

Paper linkhttps://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 普通質粒小提試劑盒

Journal: Plant Molecular Biology Reporter Published 27 January 2021

InstitutionCollege of Horticulture, Hainan University

Paper linkhttps://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 linkhttps://www.frontiersin.org/articles/10.3389/fmicb.2023.1153153/full

 


 
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