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首頁 > 核酸生(shēng)物(wù)學 > 核酸提取 > 基因組提取

全血基因組DNA小(xiǎo)量提取試劑盒

全血基因組DNA小(xiǎo)量提取試劑盒

産品編号:RTG2406

産品規格:50次

數量
價格 ¥700



全血基因組DNA小(xiǎo)量提取試劑盒

Total DLood DNA Miniprep Kit

試劑盒内容及保存:

試劑盒組成

RTG2406

50次)

貯存方式

緩沖液DL1

16 ml

常溫

緩沖液DL2

16 ml

常溫

去蛋白(bái)液GD(濃縮液)

30 ml

常溫

漂洗液PW(濃縮液)

25 ml

常溫

洗脫緩沖液EB

15 ml

常溫

吸附柱CG

50個(gè)

常溫

收集管(2 ml

50個(gè)

常溫

說明書

1

 

儲存條件(jiàn)和效期:

該試劑盒常溫貯存,常溫運輸。開(kāi)封後有效期一(yī)年(nián)。

産品簡介:

全血基因組DNA 小(xiǎo)量提取試劑盒可從(cóng)200-400 μl體積新鮮、冷凍或抗凝全血樣本中快速分離純化基因組DNA。該試劑盒可以在30分鍾内完成單個(gè)或多(duō)個(gè)樣品的操作。 提取過程無需使用蛋白(bái)酶K消化,不需要酚氯仿抽提, 也無需耗時的異丙醇沉澱等過程 。

使用該試劑盒提取到(dào)的DNA 可以用于PCR,Southern雜(zá)交,酶切消化等實驗。

準備工(gōng)作:

1. 準備無水(shuǐ)乙醇;制冰機(jī);1.5ml離心管;2ml離心管;離心機(jī)

2. 按照(zhào)标簽所示在去蛋白(bái)液GD和漂洗液PW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DL1和DL2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。

注意:以下(xià)方案适用于400 μl體積新鮮或冷凍血液樣本。如果使用低(dī)于400 μl的全血樣本,必須按比例減少緩沖液DL1和DL2的用量或者用1×PBS溶液補齊至400 μl,嚴格按照(zhào)緩沖液DL1:全血:緩沖液DL2=343體積比進行操作,否則将導緻後續操作無法進行。

1. 加入300μl緩沖液DL1于1.5 ml離心管中。

2. 加入400 μl抗凝全血,漩渦劇烈震蕩30秒(miǎo)。 注:如果低(dī)于400 μl血液,用1×PBS補齊到(dào)400 μl。

3. 加入300μl緩沖液DL2,劇烈搖動離心管3-5次,漩渦劇烈震蕩30秒(miǎo)-60秒(miǎo)。

注:加入緩沖液DL2後,會(huì)出現大量血紅(hóng)蛋白(bái)沉澱,必須劇烈震蕩。

4. 12000 rpm 離心2分鍾。

5. 把吸附柱裝在2ml收集管中(已提供),将第4步得到(dào)的上(shàng)清溶液全部轉入柱中(小(xiǎo)心别觸及沉澱),12000 rpm離心1min,倒棄流出液重新套上(shàng)收集管。

注:吸附柱的承受最大體積是700 μl,如上(shàng)清超過此體積,可分2次離心,保證所有上(shàng)清都加到(dào)柱中。

6.加入500 μl 去蛋白(bái)液GB(注意是否已經加入乙醇)至柱子中,12000 rpm離心1min,棄去流出液。

注:吸附柱膜上(shàng)會(huì)有血色素殘餘,這是正常現象,可以被去蛋白(bái)液GD和漂洗液PW洗去。

7. 将吸附柱重新套回2ml收集管中,加入700μl 漂洗液PW(注意是否已經加入乙醇)至柱子中,12000 rpm離心1min,倒棄流出液;

8. 再加入500μl 漂洗液PW至柱子中,12000 rpm離心1min, 棄去流出液;

9. 将吸附柱重新套回2ml收集管中,12000 rpm離心空結合柱2 min以幹燥柱子的基質;

注:這一(yī)步驟至關重要,不要省略。 否則殘餘乙醇會(huì)影響後續酶切或PCR實驗。

10. 将柱子置于1.5ml滅菌離心管,加入50-80 μl65℃預熱的洗脫緩沖液EB或滅菌去離子水(shuǐ)至柱子的膜中央。 常溫靜(jìng)置2 min; 

注: 洗脫緩沖液體積最好不少于50 μl,體積過小(xiǎo)影響回收效率。

  洗脫液的pH值對于洗脫效率有很大影響。若用水(shuǐ)做洗脫液應保證其pH值在7.0-8.5範圍内,pH值低(dī)于7.0會(huì)降低(dī)洗脫效率。

11. 12000 rpm離心 2 min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)問題分析:

常見(jiàn)問題

可能(néng)原因

建議

堵柱子

樣本體積不對,裂解不完全

未按照(zhào)說明書使用指定體積操作,請嚴格按照(zhào)緩沖液DL1:全血:緩沖液DL2=343體積比進行操作

回收不到(dào)DNA或得率低(dī)

堵柱子

見(jiàn)上(shàng)

化療病人全血中提取DNA

化療病人血液中白(bái)細胞數量減少,導緻DNA數量降低(dī)

全血樣品保存不當,導緻全血溶血導緻DNA降解

4℃冰箱中貯存2周的全血開(kāi)始出現溶血現象,此時DNA随貯存時間延長(cháng)會(huì)程序分解,最終導緻分離不到(dào)電(diàn)泳可見(jiàn)的DNA;全血應該-20℃或-80℃貯存。

去蛋白(bái)液GD和漂洗液PW沒有按說明書加入乙醇稀釋

使用前按說明書加入适量的無水(shuǐ)乙醇進行稀釋

DNA純度差

高(gāo)A260/A280比率接近2.0

考慮全血樣品的新鮮程度。陳舊(jiù)全血中的DNA會(huì)降解成小(xiǎo)片段DNA或核苷酸混合物(wù),導緻A260讀(dú)數變大

DNA中有RNA污染

使用非常新鮮的全血提取DNA時電(diàn)泳結果會(huì)有RNA污染,RNA不能(néng)作為(wèi)擴增模闆,不會(huì)影響PCR擴增。如要去除RNA,可在步驟1加入緩沖液DL1時同步加入5 μl RNaseA溶液(10mg/ml

洗滌時柱中有帶顔色的遺留物(wù)

未按照(zhào)說明書使用指定體積操作

請嚴格按照(zhào)緩沖液DL1:全血:緩沖液DL2=343體積比進行操作

去蛋白(bái)液GB和漂洗液PW沒有按說明書加入乙醇稀釋

使用前按說明書加入适量的無水(shuǐ)乙醇進行稀釋

 實驗示例:

400μl human blood gDNA 上(shàng)樣5μl


人血液基因組擴增人β-球蛋白(bái) 1.3kb 片段



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

InstitutionInstitute of Plant Protection ,Chinese Academy of Agricultural Sciences

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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.

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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.

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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).

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Paper link

 

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