exonuclease vii  (New England Biolabs)


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    Name:
    Exonuclease VII
    Description:
    Exonuclease VII 1 000 units
    Catalog Number:
    m0379l
    Price:
    640
    Size:
    1 000 units
    Category:
    Exonucleases
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    New England Biolabs exonuclease vii
    Exonuclease VII
    Exonuclease VII 1 000 units
    https://www.bioz.com/result/exonuclease vii/product/New England Biolabs
    Average 99 stars, based on 731 article reviews
    Price from $9.99 to $1999.99
    exonuclease vii - by Bioz Stars, 2020-04
    99/100 stars

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    Related Articles

    Multiplexing:

    Article Title: High-Resolution Analysis of the Efficiency, Heritability, and Editing Outcomes of CRISPR/Cas9-Induced Modifications of NCED4 in Lettuce (Lactuca sativa)
    Article Snippet: Dual indexing was done using the Nextera XT system (Illumina, San Diego, CA) using 16 i5 indexes (S502-S522) and 24 i7 indexes (N701-N729) enabling multiplexing of 384 individual libraries. .. Given the recent concerns of index switching during sequencing of dual index multiplexed samples using Illumina platforms , the pooled libraries were treated with Exonuclease VII (NEB, Ipswich, MA) to remove all residual single-stranded index primers, after which we performed a BluePippin (Sage Science Inc., Beverly, MA) size selection treatment for removal of all fragments smaller than 100 bp.

    Clone Assay:

    Article Title: Complete Genome Sequence and Methylome Analysis of Sphaerotilus natans subsp. sulfidivorans D-507
    Article Snippet: The Escherichia coli genomic DNAs from strains ER2796 and ER3081 with cloned methyltransferase genes were purified using the Monarch genome purification kit (New England BioLabs, Ipswich, MA). .. Incompletely formed SMRTbell templates and linear DNAs were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs).

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: It is the original source of the type II restriction enzyme BclI, which recognizes and cleaves the DNA sequence T↓GATCA, producing 5′ cohesive ends compatible for cloning DNA digested with Sau3AI (↓GATC), BamHI (G↓GATCC), or BglII (A↓GATCT) ( ). .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA).

    Concentration Assay:

    Article Title: Stochasticity enables BCR-independent germinal center initiation and antibody affinity maturation
    Article Snippet: The barcoding reaction contained 5 µl cDNA products, 8 µl of 5× HF buffer, 1 µl dNTP mixture (final concentration 250 µM each), barcode primer (final concentration 400 nM), and 0.2 µl Phusion DNA polymerase, with adjusted volume using RNase- and DNase-free water to 40 µl. .. The barcoding program was as follows: 98°C for 1 min, 55°C for 30 s, 72°C for 10 min. Extraneous barcode primers were removed with 1 µl Exonuclease VII (New England Biolabs) per 40-µl reaction, incubated at 37°C for 1 h, followed by heat-inactivation at 95°C for 15 min. First-round PCR was designed to add adaptors at the 5′ and 3′ ends of the amplicon.

    Amplification:

    Article Title: Stochasticity enables BCR-independent germinal center initiation and antibody affinity maturation
    Article Snippet: .. The barcoding program was as follows: 98°C for 1 min, 55°C for 30 s, 72°C for 10 min. Extraneous barcode primers were removed with 1 µl Exonuclease VII (New England Biolabs) per 40-µl reaction, incubated at 37°C for 1 h, followed by heat-inactivation at 95°C for 15 min. First-round PCR was designed to add adaptors at the 5′ and 3′ ends of the amplicon. ..

    Article Title: High-Resolution Analysis of the Efficiency, Heritability, and Editing Outcomes of CRISPR/Cas9-Induced Modifications of NCED4 in Lettuce (Lactuca sativa)
    Article Snippet: Paragraph title: Amplicon sequencing ... Given the recent concerns of index switching during sequencing of dual index multiplexed samples using Illumina platforms , the pooled libraries were treated with Exonuclease VII (NEB, Ipswich, MA) to remove all residual single-stranded index primers, after which we performed a BluePippin (Sage Science Inc., Beverly, MA) size selection treatment for removal of all fragments smaller than 100 bp.

    Sample Prep:

    Article Title: Complete Genome Sequence and Methylome Analysis of Sphaerotilus natans subsp. sulfidivorans D-507
    Article Snippet: Incompletely formed SMRTbell templates and linear DNAs were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs). .. A SMRTbell library was prepared according to the PacBio sample preparation protocol, which included additional separation on a BluePippin system (Sage Science, Beverly, MA), and sequenced with C4-P6 chemistry, using 2 SMRT cells, one with a non-size-selected 8-kb library and one with a size-selected 11-kb library, and a 360-minute collection time.

    Article Title: Complete Genome and Methylome Analysis of Psychrotrophic Bacterial Isolates from Lake Untersee in Antarctica
    Article Snippet: Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA). .. Four 20-kb SMRTbell libraries were prepared according to the modified PacBio sample preparation protocols, including additional separation on a BluePippin, and sequenced using C4 chemistry on 16 single-molecule real-time (SMRT) cells with a 180- to 240-min collection time.

    Article Title: Complete Genome Sequence and Methylome Analysis of Acinetobacter calcoaceticus 65
    Article Snippet: Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs; Ipswich, MA, USA). .. One 20-kb SMRTbell library was prepared according to the modified PacBio sample preparation protocols, including additional separation on a BluePippin, and sequenced using C4-P6 chemistry and three single-molecule real-time (SMRT) cells with a 240-min collection time.

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA). .. One 12-kb SMRTbell library was prepared according to the modified PacBio sample preparation protocols, including additional separation with the BluePippin system, and sequenced using C4-P6 chemistry and 3 single-molecule real-time (SMRT) cells with a 240-min collection time.

    Ligation:

    Article Title: A flexible and efficient template format for circular consensus sequencing and SNP detection
    Article Snippet: .. Failed ligation products were removed through digestion in the presence of ExoIII and ExoVII exonucleases (NEB and USB, respectively). ..

    Article Title: Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy
    Article Snippet: A SMRTbell library was prepared from the MfeI fragments by ligation for 16 hours at 16°C with a hairpin adapter containing an overhang sequence complementary to the MfeI cut site using E . coli DNA ligase (New England Biolabs). .. Genome complexity reduction was performed by incubating each sample with a mixture of restriction enzymes BamHI-HF and XhoI HF plus Exonuclease III and Exonuclease VII (New England Biolabs).

    Article Title: Dual Roles of Poly(dA:dT) Tracts in Replication Initiation and Fork Collapse
    Article Snippet: The first blunting reaction was performed using ExoVII (NEB, M0379S) for 1hr, 37C. .. After A-tailing, ligation of “END-seq hairpin adaptor 1,” listed in reagents section, using NEB Quick Ligation Kit (NEB, M2200S).

    Article Title: Long-adapter single-strand oligonucleotide probes for the massively multiplexed cloning of kilobase genome regions
    Article Snippet: Gap filling and ligation was performed for 30 min at 65 °C. .. Linear DNA Digestion Solution (volume of 48 μl) was composed of 24μl of nuclease free water, 6 μl of Exonuclease I (20 units/μl), 6 μl of Exonuclease III (100 units/μl), 6 μl of Lambda Exonuclease (5 units/μl) and 6 μl Exonuclease VII (10 units/μl) (all from NEB).

    Isolation:

    Article Title: Complete Genome and Methylome Analysis of Psychrotrophic Bacterial Isolates from Lake Untersee in Antarctica
    Article Snippet: DNA from the four isolated cultures, U13-I, U41, U17-1, and U14-5, were purified using a modified Qiagen method, and their genomes were sequenced using the Pacific Biosciences (PacBio) RSII sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Acinetobacter calcoaceticus 65
    Article Snippet: GENOME ANNOUNCEMENT The bacterial strain Acinetobacter calcoaceticus 65 (recently renamed Acinetobacter junii 65) was originally isolated from a limnetic water sample and is now housed in the New England BioLabs culture collection (NEB1023). .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs; Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: The bacterial strain Bacillus caldolyticus NEB414 was originally isolated as an extreme thermophile organism and is now housed in the New England Biolabs culture collection. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA).

    Construct:

    Article Title: Complete Genome Sequence and Methylome Analysis of Sphaerotilus natans subsp. sulfidivorans D-507
    Article Snippet: Briefly, SMRTbell libraries were constructed from a genomic DNA sample sheared to ∼10 to 20 kb using the g-Tube protocol (Covaris, Woburn, MA), end repaired, and ligated to PacBio hairpin adapters. .. Incompletely formed SMRTbell templates and linear DNAs were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs).

    Article Title: Complete Genome and Methylome Analysis of Psychrotrophic Bacterial Isolates from Lake Untersee in Antarctica
    Article Snippet: Briefly, SMRTbell libraries were constructed from a genomic DNA sample sheared to an average size of ~10 to 20 kb using the G-tubes protocol (Covaris, Woburn, MA, USA), end repaired, and ligated to hairpin adapters. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Acinetobacter calcoaceticus 65
    Article Snippet: Briefly, SMRTbell libraries were constructed from a genomic DNA sample sheared to an average size of ~10 to 20 kb using the G-tubes protocol (Covaris, Woburn, MA, USA), end repaired, and ligated to hairpin adapters. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs; Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: Briefly, SMRTbell libraries were constructed from a genomic DNA sample sheared to an average size of ~10 to 20 kb using the G-tubes protocol (Covaris, Woburn, MA, USA), end repaired, and ligated to hairpin adapters. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA).

    Purification:

    Article Title: Complete Genome Sequence and Methylome Analysis of Sphaerotilus natans subsp. sulfidivorans D-507
    Article Snippet: The Escherichia coli genomic DNAs from strains ER2796 and ER3081 with cloned methyltransferase genes were purified using the Monarch genome purification kit (New England BioLabs, Ipswich, MA). .. Incompletely formed SMRTbell templates and linear DNAs were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs).

    Article Title: Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy
    Article Snippet: No-Amp Targeted Sequencing Purified genomic DNA (20 μg) was digested with MfeI restriction enzyme (New England Biolabs) to isolate the region of interest in a 6.7 kb fragment. .. Genome complexity reduction was performed by incubating each sample with a mixture of restriction enzymes BamHI-HF and XhoI HF plus Exonuclease III and Exonuclease VII (New England Biolabs).

    Article Title: Complete Genome and Methylome Analysis of Psychrotrophic Bacterial Isolates from Lake Untersee in Antarctica
    Article Snippet: DNA from the four isolated cultures, U13-I, U41, U17-1, and U14-5, were purified using a modified Qiagen method, and their genomes were sequenced using the Pacific Biosciences (PacBio) RSII sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Acinetobacter calcoaceticus 65
    Article Snippet: Genomic DNA from a culture of A. calcoaceticus 65 was purified using a modified Qiagen method and the genome sequenced using the Pacific Biosciences (PacBio) RSII sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs; Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: Genomic DNA from a culture of B. caldolyticus NEB414 was purified using a modified Qiagen method, and the genome was sequenced using the Pacific Biosciences (PacBio) RS II sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA).

    Article Title: Long-adapter single-strand oligonucleotide probes for the massively multiplexed cloning of kilobase genome regions
    Article Snippet: After digestion, the capture reaction was purified using AMPure beads (1.8 X and washed with 70% ethanol) and eluted in 25 μl of DNAse free water. .. Linear DNA Digestion Solution (volume of 48 μl) was composed of 24μl of nuclease free water, 6 μl of Exonuclease I (20 units/μl), 6 μl of Exonuclease III (100 units/μl), 6 μl of Lambda Exonuclease (5 units/μl) and 6 μl Exonuclease VII (10 units/μl) (all from NEB).

    Sequencing:

    Article Title: Complete Genome Sequence and Methylome Analysis of Sphaerotilus natans subsp. sulfidivorans D-507
    Article Snippet: Single-molecule real-time (SMRT) libraries were sequenced using the Pacific Biosciences (PacBio) RS II sequencing platform. .. Incompletely formed SMRTbell templates and linear DNAs were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs).

    Article Title: Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy
    Article Snippet: Paragraph title: No-Amp Targeted Sequencing ... Genome complexity reduction was performed by incubating each sample with a mixture of restriction enzymes BamHI-HF and XhoI HF plus Exonuclease III and Exonuclease VII (New England Biolabs).

    Article Title: Complete Genome and Methylome Analysis of Psychrotrophic Bacterial Isolates from Lake Untersee in Antarctica
    Article Snippet: DNA from the four isolated cultures, U13-I, U41, U17-1, and U14-5, were purified using a modified Qiagen method, and their genomes were sequenced using the Pacific Biosciences (PacBio) RSII sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Acinetobacter calcoaceticus 65
    Article Snippet: Genomic DNA from a culture of A. calcoaceticus 65 was purified using a modified Qiagen method and the genome sequenced using the Pacific Biosciences (PacBio) RSII sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs; Ipswich, MA, USA).

    Article Title: Stochasticity enables BCR-independent germinal center initiation and antibody affinity maturation
    Article Snippet: Paragraph title: Library preparation and sequencing ... The barcoding program was as follows: 98°C for 1 min, 55°C for 30 s, 72°C for 10 min. Extraneous barcode primers were removed with 1 µl Exonuclease VII (New England Biolabs) per 40-µl reaction, incubated at 37°C for 1 h, followed by heat-inactivation at 95°C for 15 min. First-round PCR was designed to add adaptors at the 5′ and 3′ ends of the amplicon.

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: Genomic DNA from a culture of B. caldolyticus NEB414 was purified using a modified Qiagen method, and the genome was sequenced using the Pacific Biosciences (PacBio) RS II sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA).

    Article Title: High-Resolution Analysis of the Efficiency, Heritability, and Editing Outcomes of CRISPR/Cas9-Induced Modifications of NCED4 in Lettuce (Lactuca sativa)
    Article Snippet: .. Given the recent concerns of index switching during sequencing of dual index multiplexed samples using Illumina platforms , the pooled libraries were treated with Exonuclease VII (NEB, Ipswich, MA) to remove all residual single-stranded index primers, after which we performed a BluePippin (Sage Science Inc., Beverly, MA) size selection treatment for removal of all fragments smaller than 100 bp. .. After sequencing, we analyzed the occurrence of index switching in our datasets by demultiplexing the unused index combinations and mapping the reads to the reference.

    Polymerase Chain Reaction:

    Article Title: A flexible and efficient template format for circular consensus sequencing and SNP detection
    Article Snippet: For the the ΦX174 PCR products, the hairpin oligonucleotides consisted of the sequences 5′-CGGGTCTCTCTCTTTTCCTCCTCCTCCGTTGTTGTTGTTGAGAGAGA-3′ and 5′-CTTCTCTCTCTCTTTTCCTCCTCCTCCGTTGTTGTTGTTGAGAGAGA-3′. .. Failed ligation products were removed through digestion in the presence of ExoIII and ExoVII exonucleases (NEB and USB, respectively).

    Article Title: Stochasticity enables BCR-independent germinal center initiation and antibody affinity maturation
    Article Snippet: .. The barcoding program was as follows: 98°C for 1 min, 55°C for 30 s, 72°C for 10 min. Extraneous barcode primers were removed with 1 µl Exonuclease VII (New England Biolabs) per 40-µl reaction, incubated at 37°C for 1 h, followed by heat-inactivation at 95°C for 15 min. First-round PCR was designed to add adaptors at the 5′ and 3′ ends of the amplicon. ..

    Incubation:

    Article Title: Stochasticity enables BCR-independent germinal center initiation and antibody affinity maturation
    Article Snippet: .. The barcoding program was as follows: 98°C for 1 min, 55°C for 30 s, 72°C for 10 min. Extraneous barcode primers were removed with 1 µl Exonuclease VII (New England Biolabs) per 40-µl reaction, incubated at 37°C for 1 h, followed by heat-inactivation at 95°C for 15 min. First-round PCR was designed to add adaptors at the 5′ and 3′ ends of the amplicon. ..

    Article Title: A novel CRISPR/Cas9 associated technology for sequence-specific nucleic acid enrichment
    Article Snippet: .. Next, exonuclease III (NEB, cat. #M0206L) and exonuclease VII (NEB, cat. #M0379S) were added with NEB buffer 1 (NEB, cat. #B7001S) and incubated for a total of 240 minutes at 37°C. ..

    Article Title: Large Enriched Fragment Targeted Sequencing (LEFT-SEQ) Applied to Capture of Wolbachia Genomes
    Article Snippet: PacBio library preparation A preliminary step of single strand removal and DNA damage repair was performed using Exonuclease VII and the NEBNext® FFPE DNA Repair kit (New England Biolabs, MA, US) in a 48 μL reaction volume containing: the captured DNA (~500 ng), 5 μL of NEBNext® FFPE DNA repair buffer and 1 μL of exonuclease VII (NEB) (Fig. ). .. 2 μL of NEBNext® FFPE DNA Enzyme mix was added to the reaction and incubated 20 minutes at 37 °C.

    Selection:

    Article Title: High-Resolution Analysis of the Efficiency, Heritability, and Editing Outcomes of CRISPR/Cas9-Induced Modifications of NCED4 in Lettuce (Lactuca sativa)
    Article Snippet: .. Given the recent concerns of index switching during sequencing of dual index multiplexed samples using Illumina platforms , the pooled libraries were treated with Exonuclease VII (NEB, Ipswich, MA) to remove all residual single-stranded index primers, after which we performed a BluePippin (Sage Science Inc., Beverly, MA) size selection treatment for removal of all fragments smaller than 100 bp. .. After sequencing, we analyzed the occurrence of index switching in our datasets by demultiplexing the unused index combinations and mapping the reads to the reference.

    Formalin-fixed Paraffin-Embedded:

    Article Title: Large Enriched Fragment Targeted Sequencing (LEFT-SEQ) Applied to Capture of Wolbachia Genomes
    Article Snippet: .. PacBio library preparation A preliminary step of single strand removal and DNA damage repair was performed using Exonuclease VII and the NEBNext® FFPE DNA Repair kit (New England Biolabs, MA, US) in a 48 μL reaction volume containing: the captured DNA (~500 ng), 5 μL of NEBNext® FFPE DNA repair buffer and 1 μL of exonuclease VII (NEB) (Fig. ). .. 2 μL of NEBNext® FFPE DNA Enzyme mix was added to the reaction and incubated 20 minutes at 37 °C.

    DNA Purification:

    Article Title: Dual Roles of Poly(dA:dT) Tracts in Replication Initiation and Fork Collapse
    Article Snippet: For HCT116 cells, 7.5 million cells in single suspension were embedded in an agarose plug (1% agarose final), and DNA from two plugs were combined after DNA shearing, prior to DNA purification for library prep. .. The first blunting reaction was performed using ExoVII (NEB, M0379S) for 1hr, 37C.

    Modification:

    Article Title: Complete Genome and Methylome Analysis of Psychrotrophic Bacterial Isolates from Lake Untersee in Antarctica
    Article Snippet: DNA from the four isolated cultures, U13-I, U41, U17-1, and U14-5, were purified using a modified Qiagen method, and their genomes were sequenced using the Pacific Biosciences (PacBio) RSII sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Acinetobacter calcoaceticus 65
    Article Snippet: Genomic DNA from a culture of A. calcoaceticus 65 was purified using a modified Qiagen method and the genome sequenced using the Pacific Biosciences (PacBio) RSII sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs; Ipswich, MA, USA).

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: Genomic DNA from a culture of B. caldolyticus NEB414 was purified using a modified Qiagen method, and the genome was sequenced using the Pacific Biosciences (PacBio) RS II sequencing platform. .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA).

    Plasmid Preparation:

    Article Title: Complete Genome Sequence and Methylome Analysis of Bacillus caldolyticus NEB414
    Article Snippet: Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England Biolabs, Ipswich, MA, USA). .. Sequencing reads were processed, mapped, and assembled by the Pacific Biosciences SMRT analysis pipeline using the HGAP3 protocol and polished using Quiver ( ) to yield 943.9 Mb of sequence data, which was assembled into two contigs, a closed circular genome of 3,457,580 bp with 159.9-fold coverage and a plasmid, pBcl1, of 28,002 bp with 362.8-fold coverage.

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  • 99
    New England Biolabs exonuclease vii
    Exonuclease Vii, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/exonuclease vii/product/New England Biolabs
    Average 99 stars, based on 7 article reviews
    Price from $9.99 to $1999.99
    exonuclease vii - by Bioz Stars, 2020-04
    99/100 stars
      Buy from Supplier

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