Polymerase Chain Reaction:Article Title: Methods for indexing samples and sequencing multiple polynucleotide templates
Article Snippet: The recovered volumes were each purified with a Qiagen PCR purification kit column and eluted in 30 μl of EB. .. Step 2) End-Repair Materials: Nebulized DNA (from Step 1) Water T4 DNA ligase buffer with 10 mM ATP (10×) (NEB, B0202S) dNTPs mix (10 mM each) (NEB, N0447S) T4 DNA Polymerase (3 U/ul) (NEB, M0203L) E. coli DNA Pol I large fragment (Klenow) (5 U/ul) (NEB, M0210S) T4 polynucleotide kinase (10 U/ul) (NEB, M0201L) PCR purification kit columns (Qiagen, 28104) Procedure: End repair mix was assembled as follows: Nebulized DNA 30 μl Water 45 μl T4 DNA ligase buffer with 10 mM ATP 10 μl dNTPs 4 μl T4 DNA pol 5 μl Klenow DNA pol 1 ul T4 PNK 5 ul 100 μl total The reaction was incubated for 30 minutes at room temperature. .. The DNA was purified on a Qiagen column, eluting in 30 μl EB.
Article Title: Methods for indexing samples and sequencing multiple polynucleotide templates
Article Snippet: The recovered volumes were each purified with a Qiagen PCR purification kit column and eluted in 30 μl of EB. .. Step 2) End-Repair Materials: Nebulized DNA (from Step 1) Water T4 DNA ligase buffer with 10 mM ATP (10×) (NEB, B0202S) dNTPs mix (10 mM each) (NEB, N04475) T4 DNA Polymerase (3 U/ul) (NEB, M0203L) E. coli DNA Pol I large fragment (Klenow) (5 U/ul) (NEB, M0210S) T4 polynucleotide kinase (10 U/ul) (NEB, M0201L) PCR purification kit columns (Qiagen, 28104) Procedure: End repair mix was assembled as follows: Nebulized DNA 30 μl Water 45 μl T4 DNA ligase buffer with 10 mM ATP 10 μl dNTPs 4 μl T4 DNA pol 5 μl Klenow DNA pol 1 ul T4 PNK 5 ul 100 μl total The reaction was incubated for 30 minutes at room temperature. .. The DNA was purified on a Qiagen column, eluting in 30 μl EB.
Purification:Article Title: Methods for indexing samples and sequencing multiple polynucleotide templates
Article Snippet: The recovered volumes were each purified with a Qiagen PCR purification kit column and eluted in 30 μl of EB. .. Step 2) End-Repair Materials: Nebulized DNA (from Step 1) Water T4 DNA ligase buffer with 10 mM ATP (10×) (NEB, B0202S) dNTPs mix (10 mM each) (NEB, N0447S) T4 DNA Polymerase (3 U/ul) (NEB, M0203L) E. coli DNA Pol I large fragment (Klenow) (5 U/ul) (NEB, M0210S) T4 polynucleotide kinase (10 U/ul) (NEB, M0201L) PCR purification kit columns (Qiagen, 28104) Procedure: End repair mix was assembled as follows: Nebulized DNA 30 μl Water 45 μl T4 DNA ligase buffer with 10 mM ATP 10 μl dNTPs 4 μl T4 DNA pol 5 μl Klenow DNA pol 1 ul T4 PNK 5 ul 100 μl total The reaction was incubated for 30 minutes at room temperature. .. The DNA was purified on a Qiagen column, eluting in 30 μl EB.
Article Title: Methods for indexing samples and sequencing multiple polynucleotide templates
Article Snippet: The recovered volumes were each purified with a Qiagen PCR purification kit column and eluted in 30 μl of EB. .. Step 2) End-Repair Materials: Nebulized DNA (from Step 1) Water T4 DNA ligase buffer with 10 mM ATP (10×) (NEB, B0202S) dNTPs mix (10 mM each) (NEB, N04475) T4 DNA Polymerase (3 U/ul) (NEB, M0203L) E. coli DNA Pol I large fragment (Klenow) (5 U/ul) (NEB, M0210S) T4 polynucleotide kinase (10 U/ul) (NEB, M0201L) PCR purification kit columns (Qiagen, 28104) Procedure: End repair mix was assembled as follows: Nebulized DNA 30 μl Water 45 μl T4 DNA ligase buffer with 10 mM ATP 10 μl dNTPs 4 μl T4 DNA pol 5 μl Klenow DNA pol 1 ul T4 PNK 5 ul 100 μl total The reaction was incubated for 30 minutes at room temperature. .. The DNA was purified on a Qiagen column, eluting in 30 μl EB.
Incubation:Article Title: Methods for indexing samples and sequencing multiple polynucleotide templates
Article Snippet: The recovered volumes were each purified with a Qiagen PCR purification kit column and eluted in 30 μl of EB. .. Step 2) End-Repair Materials: Nebulized DNA (from Step 1) Water T4 DNA ligase buffer with 10 mM ATP (10×) (NEB, B0202S) dNTPs mix (10 mM each) (NEB, N0447S) T4 DNA Polymerase (3 U/ul) (NEB, M0203L) E. coli DNA Pol I large fragment (Klenow) (5 U/ul) (NEB, M0210S) T4 polynucleotide kinase (10 U/ul) (NEB, M0201L) PCR purification kit columns (Qiagen, 28104) Procedure: End repair mix was assembled as follows: Nebulized DNA 30 μl Water 45 μl T4 DNA ligase buffer with 10 mM ATP 10 μl dNTPs 4 μl T4 DNA pol 5 μl Klenow DNA pol 1 ul T4 PNK 5 ul 100 μl total The reaction was incubated for 30 minutes at room temperature. .. The DNA was purified on a Qiagen column, eluting in 30 μl EB.
Article Title: Methods for indexing samples and sequencing multiple polynucleotide templates
Article Snippet: The recovered volumes were each purified with a Qiagen PCR purification kit column and eluted in 30 μl of EB. .. Step 2) End-Repair Materials: Nebulized DNA (from Step 1) Water T4 DNA ligase buffer with 10 mM ATP (10×) (NEB, B0202S) dNTPs mix (10 mM each) (NEB, N04475) T4 DNA Polymerase (3 U/ul) (NEB, M0203L) E. coli DNA Pol I large fragment (Klenow) (5 U/ul) (NEB, M0210S) T4 polynucleotide kinase (10 U/ul) (NEB, M0201L) PCR purification kit columns (Qiagen, 28104) Procedure: End repair mix was assembled as follows: Nebulized DNA 30 μl Water 45 μl T4 DNA ligase buffer with 10 mM ATP 10 μl dNTPs 4 μl T4 DNA pol 5 μl Klenow DNA pol 1 ul T4 PNK 5 ul 100 μl total The reaction was incubated for 30 minutes at room temperature. .. The DNA was purified on a Qiagen column, eluting in 30 μl EB.
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