ex taq2 buffer Search Results


extaq premix taq 2× pcr solution  (TaKaRa)
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ex taq2 buffer  (TaKaRa)
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Ex Taq2 Buffer, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sys br primix ex taq 2 solution  (PRIMIX Corporation)
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PRIMIX Corporation sys br primix ex taq 2 solution
Sys Br Primix Ex Taq 2 Solution, supplied by PRIMIX Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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taq polymerase  (TaKaRa)
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template dna  (TaKaRa)
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dntp mixture  (TaKaRa)
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buffer  (TaKaRa)
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ex taq  (TaKaRa)
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dntp  (TaKaRa)
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betaine solution  (Millipore)
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truseq forward primer  (Illumina Inc)
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truseq reverse primer  (Illumina Inc)
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Image Search Results


Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Probing transcriptome-wide RNA structural changes dependent on the DEAD-box helicase Dbp2

doi: 10.1007/978-1-0716-0935-4_18

Figure Lengend Snippet:

Article Snippet: Set up a PCR reaction as below: Component Volume (μL) Final quantity Ligated cDNA (or water for primer-dimer control) 5 μL ? dNTP mixture, 2.5 mM (provided with Takara Ex Taq) 2 0.2 mM Ex Taq buffer, 10X 2.5 1X Illumina TruSeq forward primer (5 μM) 1 0.2 μM Illumina TruSeq reverse primer (5 μM) 1 0.2 μM TaKaRa Ex Taq (50 U/μL) 0.5 0.1 U/μL Nuclease-free water 13 13 μL Open in a separate window Amplify the cDNAs by PCR using the following conditions ( Note 9 ).

Techniques: Purification

Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Probing transcriptome-wide RNA structural changes dependent on the DEAD-box helicase Dbp2

doi: 10.1007/978-1-0716-0935-4_18

Figure Lengend Snippet:

Article Snippet: Set up a PCR reaction as below: Component Volume (μL) Final quantity Ligated cDNA (or water for primer-dimer control) 5 μL ? dNTP mixture, 2.5 mM (provided with Takara Ex Taq) 2 0.2 mM Ex Taq buffer, 10X 2.5 1X Illumina TruSeq forward primer (5 μM) 1 0.2 μM Illumina TruSeq reverse primer (5 μM) 1 0.2 μM TaKaRa Ex Taq (50 U/μL) 0.5 0.1 U/μL Nuclease-free water 13 13 μL Open in a separate window Amplify the cDNAs by PCR using the following conditions ( Note 9 ).

Techniques:

Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Probing transcriptome-wide RNA structural changes dependent on the DEAD-box helicase Dbp2

doi: 10.1007/978-1-0716-0935-4_18

Figure Lengend Snippet:

Article Snippet: Set up a PCR reaction as below: Component Volume (μL) Final quantity Ligated cDNA (or water for primer-dimer control) 5 μL ? dNTP mixture, 2.5 mM (provided with Takara Ex Taq) 2 0.2 mM Ex Taq buffer, 10X 2.5 1X Illumina TruSeq forward primer (5 μM) 1 0.2 μM Illumina TruSeq reverse primer (5 μM) 1 0.2 μM TaKaRa Ex Taq (50 U/μL) 0.5 0.1 U/μL Nuclease-free water 13 13 μL Open in a separate window Amplify the cDNAs by PCR using the following conditions ( Note 9 ).

Techniques:

Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Probing transcriptome-wide RNA structural changes dependent on the DEAD-box helicase Dbp2

doi: 10.1007/978-1-0716-0935-4_18

Figure Lengend Snippet:

Article Snippet: Set up a PCR reaction as below: Component Volume (μL) Final quantity Ligated cDNA (or water for primer-dimer control) 5 μL ? dNTP mixture, 2.5 mM (provided with Takara Ex Taq) 2 0.2 mM Ex Taq buffer, 10X 2.5 1X Illumina TruSeq forward primer (5 μM) 1 0.2 μM Illumina TruSeq reverse primer (5 μM) 1 0.2 μM TaKaRa Ex Taq (50 U/μL) 0.5 0.1 U/μL Nuclease-free water 13 13 μL Open in a separate window Amplify the cDNAs by PCR using the following conditions ( Note 9 ).

Techniques:

Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Probing transcriptome-wide RNA structural changes dependent on the DEAD-box helicase Dbp2

doi: 10.1007/978-1-0716-0935-4_18

Figure Lengend Snippet:

Article Snippet: Set up a PCR reaction as below: Component Volume (μL) Final quantity Ligated cDNA (or water for primer-dimer control) 5 μL ? dNTP mixture, 2.5 mM (provided with Takara Ex Taq) 2 0.2 mM Ex Taq buffer, 10X 2.5 1X Illumina TruSeq forward primer (5 μM) 1 0.2 μM Illumina TruSeq reverse primer (5 μM) 1 0.2 μM TaKaRa Ex Taq (50 U/μL) 0.5 0.1 U/μL Nuclease-free water 13 13 μL Open in a separate window Amplify the cDNAs by PCR using the following conditions ( Note 9 ).

Techniques: