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The PCRs were carried out in tripli
The PCRs were carried out in triplicate 20 mL reactions with 0.5 mMforward and reverse primers, 5 ng of template DNA, 1 PCR buffer II (Takara, Japan), 0.2mMdNTPs, 2.5 U of Pfu DNA polymerase (MBI fermentas, USA).
The PCRs were carried out in triplicate 20 mL reactions with 0.5 mMforward and reverse primers, 5 ng of template DNA, 1 PCR buffer II (Takara, Japan), 0.2mMdNTPs, 2.5 U of Pfu DNA polymerase (MBI fermentas, USA).
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Results (
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PCRs ได้ดำเนินการในปฏิกิริยา triplicate 20 mL mMforward และไพรเมอร์ย้อน 5 0.5 ng ของแม่แบบดีเอ็นเอ 1 PCR บัฟเฟอร์ II (Takara ญี่ปุ่น), 0.2mMdNTPs, 2.5 U ของ Pfu ดีเอ็นเอพอลิเมอเรส (MBI fermentas สหรัฐอเมริกา)
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Results (
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PCRs ได้ดำเนินการใน 20 เพิ่มขึ้นสามเท่าปฏิกิริยามิลลิลิตร 0.5 mMforward และไพรย้อนกลับ 5 อำเภอของดีเอ็นเอแม่แบบที่ 1? บัฟเฟอร์ PCR II (Takara, ญี่ปุ่น), 0.2mMdNTPs 2.5 U ของ Pfu ดีเอ็นเอโพลิเมอร์ (MBI Fermentas สหรัฐอเมริกา)
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Results (
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การ pcrs ทดลองปฏิกิริยา 20 ml ทำสำเนาสามฉบับ 0.5 mmforward และ reverse primers , 5 ของดีเอ็นเอแม่แบบ 1 PCR buffer 2 ( Takara , ญี่ปุ่น ) , 0.2mmdntps 2.5 U ของดีเอ็นเอพอลิเมอเรสพีเอฟยู ( 2 fermentas , USA )
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J'aime passer du temps dans divers endro
cross total
нету врагов
maybe
Sedentary lifestyle
These methods are helpful for us to unde
The conditions of the HPLC analysis were
ม้านิลมังกร เป็นสัตว์ลูกผสม พ่อเป็นมังกร
because no enemies
At present, these technologies have been
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Food quality, policy, and advertisingIn
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Food quality, policy, and advertisingIn
หน้าจอ
In this paper, 16S rDNA-PCR technique wa
Tambang emas
Act in a play
2.4.2. Analysis of amino acids by HPLC
The samples were diluted five times by t
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