RealPure植物基因組DNA提取試劑盒
貨號(hào)
|
名稱
|
規(guī)格
|
RTG2404-01
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RealPure植物基因組DNA提取試劑盒
|
50次
|
● 試劑盒內(nèi)容:
試劑盒組成
|
RTG2404-01(50次)
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緩沖液AP1
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25 ml
|
緩沖液AP2
|
10 ml
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緩沖液AP3(濃縮液)
|
15 ml
|
漂洗液PW(濃縮液)
|
25 ml
|
洗脫緩沖液EB
|
15 ml
|
RNase A(10
mg/ml)
|
0.5 ml
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吸附柱CG(白色)
|
50個(gè)
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過濾柱CF
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50個(gè)
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收集管
|
100個(gè)
|
說明書
|
1份
|
● 儲(chǔ)存條件和效期:
本試劑盒在常溫(25℃左右)干燥條件下,可保存1年;更長(zhǎng)時(shí)間的保存可置于2–8℃。2–8℃保存條件下,若溶液產(chǎn)生沉淀,應(yīng)在使用前置于37℃下溶解沉淀至溶液澄清后再使用。
單獨(dú)包裝的RNaseA收到后-20℃保存。
● 產(chǎn)品簡(jiǎn)介:
本試劑盒采用可以特異性結(jié)合DNA的離心吸附柱和獨(dú)特的緩沖液系統(tǒng),能提取多種植物細(xì)胞/組織中的基因組DNA。離心吸附柱可以高效、專一吸附DNA,可最大限度去除雜質(zhì)蛋白及細(xì)胞中其他有機(jī)化合物。提取的基因組DNA片段大,純度高,質(zhì)量穩(wěn)定可靠。
使用本試劑盒回收的DNA可適用于各種常規(guī)操作,包括酶切、PCR、文庫構(gòu)建、Southern雜交等實(shí)驗(yàn)。
● 提取得率:
材料
|
DNA得量(μg/100mg)
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Arabidopsis
|
3–4 μg
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Barley
|
8–12 μg
|
Maize
|
15-20
|
Pine
|
20-25
|
Potato
|
4-6
|
Rape
|
2-4
|
Spinach
|
5-10
|
Tobacco
|
20-25
|
Wheat
|
25-30
|
● 準(zhǔn)備工作:
1. 準(zhǔn)備液氮;65℃水浴;無水乙醇;1.5ml滅菌離心管。
2. 按照標(biāo)簽所示在緩沖液AP3和漂洗液PW中加入無水乙醇,混勻后蓋緊瓶蓋后常溫貯存?zhèn)溆谩?
3. 每次使用前請(qǐng)檢查緩沖液AP1,緩沖液AP2和緩沖液AP3是否有沉淀生成,如果出現(xiàn)沉淀,37℃溫浴至沉淀溶解后再使用。
● 操作步驟:
如非指出,所有離心步驟均為使用臺(tái)式離心機(jī)在常溫下離心。
1. 取適量植物新鮮組織0.5-1g加入液氮充分研磨,取約100mg粉末置于1.5ml離心管中,加入400 μl 緩沖液AP1和6
μl RNaseA (10mg/ml),漩渦震蕩1分鐘。
2. 將離心管放在65℃水浴10分鐘,水浴過程中顛倒離心管以混合樣品數(shù)次。
3. 加入130
μl 緩沖液AP2,顛倒混勻,冰浴5分鐘。
4. 12,000rpm離心5分鐘。
注:此步驟離心去除去垢劑,蛋白以及多糖等雜質(zhì)。
5. 取上清(通常為400
μl)轉(zhuǎn)移到過濾柱CF中,12,000rpm
離心1分鐘。
6. 將濾出液轉(zhuǎn)移到1.5
ml離心管中,加入1.5倍體積(例如400
μl的上清液加600 μl緩沖液AP3)緩沖液AP3(使用前請(qǐng)注意是否已經(jīng)加入無水乙醇),立即顛倒混勻,簡(jiǎn)短離心以去除管蓋內(nèi)壁的水珠。
7.吸取步驟6中的混合液加入到吸附柱CG中(吸附柱放入收集管中),12,000
rpm離心1分鐘,倒掉廢液,吸附柱CG放回收集管中。
注:離心吸附柱的最大容積是700μl,如果一次不能完全上柱,可以分次上柱離心,保證全部溶液全部加到離心柱中。
8.向吸附柱CG中加入500
μl漂洗液PW(使用前請(qǐng)先檢查是否已加入無水乙醇),12,000 rpm離心1分鐘,倒掉廢液,吸附柱CG放入收集管中。
9.重復(fù)步驟8。
10. 可選步驟:如果離心柱的吸附膜上有顏色,向吸附柱CG中加入500
μl無水乙醇,12,000 rpm離心1分鐘,倒掉廢液,吸附柱CG放入收集管中。
11.將吸附柱CG放回廢液收集管中,12,000 rpm離心2分鐘。
注:此步驟非常重要,目的是將吸附柱中殘余的漂洗液去除。漂洗液中乙醇的殘留會(huì)影響后續(xù)的酶反應(yīng)(酶切、PCR等)實(shí)驗(yàn)。
12.將吸附柱CG轉(zhuǎn)入一個(gè)干凈的1.5ml離心管中,向吸附膜的中間部位懸空滴加50-100 μl經(jīng)65℃水浴預(yù)熱的洗脫緩沖液EB,常溫放置2分鐘,12,000
rpm g離心2分鐘。
注;1. 洗脫緩沖液體積最好不少于50 μl,體積過小影響回收效率。
2. 洗脫液的pH值對(duì)于洗脫效率有很大影響。若用水做洗脫液應(yīng)保證其pH值在7.0-8.5范圍內(nèi),pH值低于7.0會(huì)降低洗脫效率。
13. DNA產(chǎn)物-20℃保存。
● DNA濃度及純度檢測(cè):
基因組DNA片段的大小與樣品保存時(shí)間、操作過程中的剪切力等因素有關(guān)。提取的DNA片段可用瓊脂糖凝膠電泳和紫外分光光度計(jì)檢測(cè)濃度與純度??膳渲?.8-1.0%瓊脂糖凝膠,使用λ/HindIII判斷基因組的大小,完整的基因組大小應(yīng)在23kb以上。使用分光光度計(jì)檢測(cè)時(shí),
OD260/OD280比值應(yīng)為1.7–1.9之間,如果洗脫時(shí)不使用洗脫緩沖液,而使用去離子水洗脫,比值可能偏低,但并不表明DNA純度不高。
核酸提取產(chǎn)品發(fā)表文章
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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
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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)
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Institution:China
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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
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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
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Product: RTP2202 PCR產(chǎn)物純化試劑盒
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Journal: Mol Biol Rep (2013) 40:97–107
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Journal: Appl Biochem Biotechnol (2014)
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