植物原生質(zhì)體轉(zhuǎn)化試劑盒
貨號(hào)
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名稱
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包裝
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RTU4092
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植物原生質(zhì)體轉(zhuǎn)化試劑盒
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40次
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● 產(chǎn)品組成:
序號(hào)
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組分貨號(hào)
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名稱
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規(guī)格
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貯存
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運(yùn)輸
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1
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RTU4092-01
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轉(zhuǎn)化終止溶液
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50
ml
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-20℃
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RT
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2
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RTU4092-02
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轉(zhuǎn)化試劑
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5
ml
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-20℃
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RT
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3
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RTU4092-03
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培養(yǎng)溶液
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50
ml
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-20℃
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RT
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4
|
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說(shuō)明書
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一份
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|
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● 產(chǎn)品簡(jiǎn)介:
植物原生質(zhì)體是指脫去全部細(xì)胞壁由質(zhì)膜包被的具有生命活力的裸露細(xì)胞。它具有細(xì)胞生命特征和全能型,是細(xì)胞無(wú)性系變異和突變體篩選的重要來(lái)源,同時(shí)也是植物遺傳工程的理想受體和遺傳改良的理想材料。植物原生質(zhì)體轉(zhuǎn)化試劑盒(Plant Protoplasts Transformation Kit)采用的是聚乙二醇轉(zhuǎn)化方法,借助聚乙二醇短時(shí)間內(nèi)對(duì)原生質(zhì)體產(chǎn)生的沖擊效應(yīng),使質(zhì)粒DNA、RNA或蛋白得以進(jìn)入原生質(zhì)體,經(jīng)轉(zhuǎn)化的植物原生質(zhì)體經(jīng)過(guò)一定時(shí)間培養(yǎng)后,可用于檢測(cè)外源基因的表達(dá)和功能,轉(zhuǎn)化后基因敲除或基因編輯效果等。
對(duì)于擬南芥原生質(zhì)體,使用本試劑盒轉(zhuǎn)化質(zhì)粒后通常2-6小時(shí)可以檢測(cè)相關(guān)基因的轉(zhuǎn)錄變化(mRNA等RNA的變化),通常2-16小時(shí)后可以檢測(cè)到相關(guān)蛋白表達(dá)的變化,通常24小時(shí)可以檢測(cè)到基因編輯的效果。
本試劑盒可以用于相當(dāng)于6孔板40個(gè)孔的樣品,12孔板20個(gè)孔的樣品,或24孔板40個(gè)孔的樣品的轉(zhuǎn)化。
本試劑盒不含有原生質(zhì)體制備試劑,需要制備原生質(zhì)體請(qǐng)參見(jiàn)植物原生質(zhì)體制備試劑盒(RTU4082 )。
● 貯存和效期:
按照溫度貯存,有效期一年。轉(zhuǎn)化試劑現(xiàn)用現(xiàn)配。
試劑盒常溫運(yùn)輸。
● 使用說(shuō)明:
需要準(zhǔn)備的材料(試劑盒不提供):
平頭鑷子;一次性刀片;50ml離心管;1.5ml離心管;水浴鍋
一、原生質(zhì)體轉(zhuǎn)化步驟:
1. 轉(zhuǎn)化溶液配制:
植物原生質(zhì)體轉(zhuǎn)化參考下表根據(jù)樣品量配制轉(zhuǎn)化溶液。
轉(zhuǎn)化溶液現(xiàn)用現(xiàn)配。轉(zhuǎn)化溶液需要在轉(zhuǎn)化前至少1小時(shí)配制,以確保轉(zhuǎn)化試劑溶解充分。轉(zhuǎn)化溶液配制后盡量當(dāng)天使用。配制好的轉(zhuǎn)化溶液4℃保存3-5天之內(nèi)仍然有較好的轉(zhuǎn)化效率,但和當(dāng)天配制的轉(zhuǎn)化溶液相比,轉(zhuǎn)化效果可能會(huì)有一定程度的下降。
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120 μl
(1個(gè)樣品)
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1.2 ml
(10個(gè)樣品)
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5 ml
(約40個(gè)樣品)
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轉(zhuǎn)化試劑粉末
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48
mg
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480
mg
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2
g
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轉(zhuǎn)化試劑溶解液(2×)
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60
μl
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0.6
ml
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2.5
ml
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滅菌水
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定容至120 μl
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定容至1.2 ml
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定容至5 ml
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2. 準(zhǔn)備質(zhì)粒:
取10 μl質(zhì)粒DNA(10-20
μg,濃度為1-2 μg/μl)于1.5 ml 離心管中。
注:質(zhì)粒大小建議為5-10
kb,質(zhì)粒濃度為1-2 μg/μl左右;原生質(zhì)體轉(zhuǎn)化對(duì)于質(zhì)粒的純度要求較高,盡量使用高純度的質(zhì)粒。多個(gè)質(zhì)粒同時(shí)轉(zhuǎn)化時(shí)的體積和總質(zhì)量保持不變。多個(gè)質(zhì)粒轉(zhuǎn)化時(shí),每種質(zhì)粒的用量比例,需要酌情自行調(diào)整。質(zhì)粒轉(zhuǎn)化也可以在12或24孔板中進(jìn)行,轉(zhuǎn)化體系也可以按照比例放大或縮小。本試劑盒中描述的用量相當(dāng)于是6孔板中的用量。原生質(zhì)體用多孔板培養(yǎng)時(shí),最好選擇未經(jīng)表面處理的多孔板。對(duì)于經(jīng)過(guò)表面處理的動(dòng)物細(xì)胞培養(yǎng)用多孔板,可以使用5%胎牛血清或小牛血清處理孔表面數(shù)秒,這樣有助于減小孔底表面對(duì)于原生質(zhì)體的損傷。
3. 質(zhì)粒轉(zhuǎn)化:
3.1 質(zhì)粒管中加入100 μl原生質(zhì)體溶液(原生質(zhì)體密度為2×105/ml,約2萬(wàn)個(gè)原生質(zhì)體),輕柔混勻。
3.2 加入等體積即110 μl 步驟1事先準(zhǔn)備好的轉(zhuǎn)化溶液,輕彈管底,輕柔混勻,常溫25℃放置5-15分鐘。
注:最長(zhǎng)可以孵育15 min,但通常孵育5min時(shí)間已經(jīng)足夠。最佳的孵育時(shí)間對(duì)于不同的原生質(zhì)體和不同的質(zhì)粒需要通過(guò)實(shí)驗(yàn)摸索。
4. 終止轉(zhuǎn)化:
加入2倍體積轉(zhuǎn)化終止溶液即440 μl,輕柔徹底混勻,終止轉(zhuǎn)化過(guò)程。
5. 收集原生質(zhì)體:
常溫100g離心1-2分鐘,盡量去除上清。
注:由于轉(zhuǎn)化后的溶液會(huì)非常粘稠,加入轉(zhuǎn)化終止溶液后離心1 min通??梢允乖|(zhì)體聚集在管底,但使用某些突變體時(shí)為減少原生質(zhì)體損失,可將離心時(shí)間延長(zhǎng)到2 min。為了避免原生質(zhì)體離心時(shí)貼在管壁,建議整個(gè)實(shí)驗(yàn)過(guò)程使用水平轉(zhuǎn)頭;離心時(shí),可調(diào)低離心機(jī)的升速和降速。升速過(guò)快,原生質(zhì)體可能離到管壁上;降速過(guò)快,可能導(dǎo)致管底原生質(zhì)體懸起。建議升速和降速分別都使用3。
6. 原生質(zhì)體漂洗:
加入500 μl 轉(zhuǎn)化終止溶液輕輕重懸原生質(zhì)體,常溫100g離心1 min,盡量去除殘留的上清。
注:本步驟可以充分去除殘留的轉(zhuǎn)化試劑溶液中的組分,避免轉(zhuǎn)化試劑溶液中的組分對(duì)于后續(xù)的不良影響。
7. 原生質(zhì)體重懸:
沉淀中加入1
ml培養(yǎng)溶液,輕柔重懸。
8. 原生質(zhì)體培養(yǎng):
將離心管水平放置,23-25oC弱光培養(yǎng)。
注:根據(jù)實(shí)驗(yàn)需求確定孵育時(shí)間。RNA分析孵育2-6小時(shí);酶活性分析和蛋白標(biāo)記實(shí)驗(yàn)孵育2-16小時(shí);基因編輯的效果在轉(zhuǎn)化24小時(shí)后可能被檢測(cè)到。
使用植物原生質(zhì)體轉(zhuǎn)化試劑盒轉(zhuǎn)化擬南芥原生質(zhì)體的效果圖。
實(shí)驗(yàn)步驟:稱取0.48
g轉(zhuǎn)化試劑于2 ml 離心管中,加入轉(zhuǎn)化試劑溶解液后,顛倒混勻,蒸餾水定容至2 ml,使轉(zhuǎn)化試劑充分溶解后備用。在2 ml的圓底離心管中加入10 μl(20 μg)EGFP質(zhì)粒
(植物用綠色熒光蛋白),加入100 μl制備好的原生質(zhì)體,輕柔混勻后加入110 μl當(dāng)日配制好的轉(zhuǎn)化試劑溶液,輕柔混勻,常溫靜置5
min后加入440 μl轉(zhuǎn)化終止溶液終止轉(zhuǎn)化,輕輕顛倒混勻,常溫100 g離心1
min,去除上清,再加入0.5 ml 轉(zhuǎn)化終止溶液,輕柔重懸原生質(zhì)體,常溫100
g離心1 min后,盡量去除上清,收集原生質(zhì)體。加入1 ml培養(yǎng)溶液,小心重懸原生質(zhì)體后水平放置25℃培養(yǎng)過(guò)夜(約16h),次日于熒光顯微鏡下檢測(cè)EGFP熒光信號(hào)。
植物原生質(zhì)體提取試劑盒發(fā)表文章列表
1. [IF=3.19] TaEXPB7-B,a
-expansin gene involved in low-temperature stress and abscisic acid
responses, promotes growth and cold resistance in Arabidopsis thaliana.
實(shí)驗(yàn)植物:小麥
Author: Xu Feng, Yongqing Xu, Lina
Peng, Xingyu Yu, Qiaoqin Zhao, Shanshan Feng, Ziyi Zhao, Fenglan Li,
Baozhong Hu.
Journal: J Plant Physiology 2019
Institution: College
of Life Sciences, Northeast Agricultural University
Paper link:http://www.plantphysiol.org/content/174/4/2487
2. [IF=5.36] Involvement of the
chloroplast gene ferredoxin 1 in multiple responses of Nicotiana benthamiana to
Potato virus X infection.
實(shí)驗(yàn)植物:煙草
Author: Xue Yang, Yuwen Lu, Fang Wang,
Ying Chen, Yanzhen Tian, Liangliang Jiang, Jiejun Peng, Hongying Zheng,
Lin Lin, Chengqi Yan, Michael Taliansky, Stuart MacFarlane, Yuanhua Wu,
Jianping Chen and Fei Yan
Journal: Journal of Experimental
Botany, 2020,Vol.71,
No. 6,2142–2156,
Institution:Institute
of Plant Virology, Ningbo University
Paper link:https://academic.oup.com/jxb/article/71/6/2142/5686178?login=true
3. [IF=7.228] Turnip mosaic
virus impairs perinuclear chloroplast clustering to facilitate viral infection
實(shí)驗(yàn)植物:煙草
Author:Yushan Zhai, Quan Yuan, Shiyou Qiu,
Saisai Li, Miaomiao Li, Hongying Zheng, Guanwei Wu, Yuwen Lu, Jiejun Peng,
Shaofei Rao, Jianping Chen, Fei Yan
Journal: Plant Cell Enviroment, 2021,30
July
Institution:Institute
of Plant Virology, Ningbo University
Paper link:https://onlinelibrary.wiley.com/doi/10.1111/pce.14157
4. [IF=5.64] A Novel, Small
Cysteine-Rich Effector, RsSCR10 in Rhizoctonia solani Is Sufficient to Trigger
Plant Cell Death
實(shí)驗(yàn)植物:水稻
Author:Xianyu Niu, Guijing Yang, Hui Lin,
Yao Liu, Ping Li and Aiping Zheng
Journal: Fronties in Microbiology August
2021 | Volume 12 | Article 684923
Institution:Sichuan
Agricultural University
Paper link:https://www.frontiersin.org/articles/10.3389/fmicb.2021.684923/full
5. [IF=9.8] Synthesis of
flavour-related linalool is regulated by PpbHLH1 and associated with changes in
DNA methylation during peach fruit ripening
實(shí)驗(yàn)植物:煙草
Author: Chunyan Wei, Hongru Liu,
Xiangmei Cao, Minglei Zhang, Xian Li, Kunsong Chen and Bo Zhang
Journal: Plant Biotechnology
Journal (2021) 19, pp. 2082–2096
Institution:Laboratory
of Fruit Quality Biology/Zhejiang Provincial Key Laboratory of Horticultural
Plant Integrative Biology, Zhejiang University
Paper link:https://onlinelibrary.wiley.com/doi/10.1111/pbi.13638
6. [2020IF=1.04] EoPHR2, a
Phosphate Starvation Response Transcription Factor, Is Involved in Improving
Low-Phosphorus Stress Resistance in Eremochloa ophiuroides
實(shí)驗(yàn)植物:擬南芥
Author: Ying Chen1,#, Chuanqiang
Liu1,#, Qingqing He1, Jianjian Li2, Jingjing Wang2, Ling Li2, Xiang Yao2,
Shenghao Zhou3, Haoran Wang
Journal: Phyton Vol.91, No.3, 2022,
pp.651-665
Institution: Institute
of Botany, Jiangsu Province and Chinese Academy of Sciences
Paper link:https://www.techscience.com/phyton/v91n3/45309
7. [2021IF=3.2] Establishment
and optimization of PEG-mediated protoplast transformation in the microalga Haematococcus
pluvia
實(shí)驗(yàn)材料:雨生紅球藻 Haematococcus
pluvia
Author: Chunli Guo,Muhammad
Anwar, Rui Mei,Xinyi
Li, Di Zhao,Yanan
Jiang, Jieyi
Zhuang, Chen Liu,Chaogang
Wang, Zhangli
Hu
Journal: Journal of Applied
Phycology. Published
online 07 March 2022
Institution:College
of Optoelectronic Engineering, Shenzhen University
Paper link: https://link.springer.com/article/10.1007/s10811-022-02718-x
8. [2021 IF=5.9] The Genome-Wide
Identification of Long Non-Coding RNAs Involved in Floral Thermogenesis in
Nelumbo nucifera Gaertn
實(shí)驗(yàn)材料:睡蓮 Nelumbo nucifera Gaertn
Author: Jing Jin , Yu Zou, Ying Wang,
Yueyang Sun, Jing Peng and Yi Ding
Journal: Int. J. Mol. Sci. 2022, 23, 4901.
Institution:College
of Life Sciences, Guizhou University,College
of Life Sciences, Wuhan University
Paper link: https://www.mdpi.com/1422-0067/23/9/4901
9. [2021 IF=17.9] Genome-wide association
analysis reveals a novel pathway mediated by a dual-TIR
domainprotein for pathogen resistance in cotton
實(shí)驗(yàn)材料:棉花
Author: Yihao Zhang, Yaning Zhang,
Xiaoyang Ge, Yuan Yuan, Yuying Jin, Ye Wang, Lihong Zhao, Xiao Han, Wei Hu, Lan
Yang, Chenxu Gao, Xi Wei, Fuguang Li, Zhaoen Yang
Journal: Genome Biology (2023) 24:111
Institution:Institute
of Cotton Research, Chinese Academy of Agricultura Sciences
Paper link: https://doi.org/10.1186/s13059-023-02950-9
10.
[2022 IF=7.4] Rose long noncoding RNA lncWD83 promotes flowerin by modulating
ubiquitination of the floral repressor RcMYC2L
實(shí)驗(yàn)材料:Rose 玫瑰
Author: Chen Yeqing ,Lu Jun ,Wang Weinan ,Fan Chunguo ,Yuan Guozhen ,Sun Jingjing ,Liu
Jinyi ,Wang Changquan
Journal: Plant Physiol (2023) Published: 19 September 2023
Institution:College of Horticulture, Nanjing
Agricultural University
Paper link: https://doi.org/10.1093/plphys/kiad502