exonuclease iii  (New England Biolabs)


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  • 99
    Name:
    Exonuclease VII
    Description:
    Exonuclease VII 1 000 units
    Catalog Number:
    M0379L
    Price:
    628
    Size:
    1 000 units
    Category:
    Exonucleases
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    Structured Review

    New England Biolabs exonuclease iii
    Exonuclease VII
    Exonuclease VII 1 000 units
    https://www.bioz.com/result/exonuclease iii/product/New England Biolabs
    Average 99 stars, based on 27 article reviews
    Price from $9.99 to $1999.99
    exonuclease iii - by Bioz Stars, 2019-07
    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 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).

    In Vivo:

    Article Title: Complete Genome Sequence of the Freshwater Colorless Sulfur Bacterium Beggiatoa leptomitiformis Neotype Strain D-402T
    Article Snippet: However, due to the difficulties of isolating, purifying, and growing this bacterium in vivo , only a few draft genome sequences have been assembled (accession no. NZ_AHMA00000000.1, GCA_000170695.1, and GCA_000170715.1). .. Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA).

    Amplification:

    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.

    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. .. Amplifications for heavy and light chain were done in separate reactions.

    Sample Prep:

    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). .. Qualification and quantification of genomic DNA fragments and SMRTbell libraries were performed using a Qubit fluorimeter (Invitrogen, Eugene, OR, USA) and a 2100 Bioanalyzer (Agilent, Santa Clara, CA, USA).

    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). .. Genomic DNA fragments and SMRTbell library qualification and quantification were performed using a Qubit fluorimeter (Invitrogen, Eugene, OR) and a 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).

    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). .. Genomic DNA fragments and SMRTbell libraries qualification and quantification were performed using the Qubit fluorimeter (Invitrogen, Eugene, OR) and 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).

    In Vitro:

    Article Title: Initiation, Elongation, and Realignment during Influenza Virus mRNA Synthesis
    Article Snippet: Paragraph title: In vitro capped oligonucleotide extension assay. ... To remove the excess primer, the DNA was treated with exonuclease VII (NEB) for 1 h and subsequently heated to 95°C for 10 min to denature the exonuclease.

    Modification:

    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: 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 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 of the Freshwater Colorless Sulfur Bacterium Beggiatoa leptomitiformis Neotype Strain D-402T
    Article Snippet: Incompletely formed SMRTbell templates were digested with a combination of exonuclease III and exonuclease VII (New England BioLabs, Ipswich, MA, USA). .. Genomic DNA fragments and SMRTbell library qualification and quantification were performed using a Qubit fluorimeter (Invitrogen, Eugene, OR) and 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).

    Ligation:

    Article Title: Long-adapter single-strand oligonucleotide probes for the massively multiplexed cloning of kilobase genome regions
    Article Snippet: 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). .. 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).

    Article Title: A flexible and efficient template format for circular consensus sequencing and SNP detection
    Article Snippet: Annealed hairpins were added at molar excess relative to the insert and ligated using T4 DNA Ligase (NEB). .. Failed ligation products were removed through digestion in the presence of ExoIII and ExoVII exonucleases (NEB and USB, respectively). .. To confirm the proper ligation of the inserts, extension reactions were performed in a similar method to that described previously ( ).

    Isolation:

    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).

    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: Initiation, Elongation, and Realignment during Influenza Virus mRNA Synthesis
    Article Snippet: The isolated RNA was next polyadenylated with poly(A) polymerase (NEB), reverse transcribed with the dTGG primer (5′-CACGACGCTCTTCCGATCTTTTTTTTTTTTTTTTTTGG-3′), and turned into double-stranded DNA (dsDNA) by using second-strand primer 2ND_GA (5′-GTTCAGACGTGTGCTCTTCCGATCTGA+AT+A+CTCAAG-3′ [here “+” indicates a locked nucleic acid (LNA) base]). .. To remove the excess primer, the DNA was treated with exonuclease VII (NEB) for 1 h and subsequently heated to 95°C for 10 min to denature the exonuclease.

    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: Sequence analysis was done using CrispRVariants ( ). .. 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.

    Construct:

    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).

    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 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).

    Purification:

    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).

    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: 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 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 of the Freshwater Colorless Sulfur Bacterium Beggiatoa leptomitiformis Neotype Strain D-402T
    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), additionally purified using the PowerClean DNA clean-up kit (MoBio Laboratories, Inc., Carlsbad, CA), 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).

    Sequencing:

    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: 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 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: High-Resolution Analysis of the Efficiency, Heritability, and Editing Outcomes of CRISPR/Cas9-Induced Modifications of NCED4 in Lettuce (Lactuca sativa)
    Article Snippet: Sequence analysis was done using CrispRVariants ( ). .. 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.

    Article Title: Initiation, Elongation, and Realignment during Influenza Virus mRNA Synthesis
    Article Snippet: To sequence the extended capped primers, products were excised from the 20% denaturing PAGE gel, eluted overnight in water and desalted over NAP-10 columns (GE Healthcare). .. To remove the excess primer, the DNA was treated with exonuclease VII (NEB) for 1 h and subsequently heated to 95°C for 10 min to denature the exonuclease.

    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.

    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.

    Incubation:

    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. .. Amplifications for heavy and light chain were done in separate reactions.

    RAST Test:

    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). .. Sequencing reads were processed, mapped, and assembled by the Pacific Biosciences SMRT Analysis pipeline using the HGAP3 protocol and polished using Quiver ( ) to yield six fully closed genomes, including nine plasmids ( ).

    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). .. 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.

    Article Title: Complete Genome Sequence of the Freshwater Colorless Sulfur Bacterium Beggiatoa leptomitiformis Neotype Strain D-402T
    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 give a fully closed genome with 422× coverage.

    Polyacrylamide Gel Electrophoresis:

    Article Title: Initiation, Elongation, and Realignment during Influenza Virus mRNA Synthesis
    Article Snippet: To sequence the extended capped primers, products were excised from the 20% denaturing PAGE gel, eluted overnight in water and desalted over NAP-10 columns (GE Healthcare). .. To remove the excess primer, the DNA was treated with exonuclease VII (NEB) for 1 h and subsequently heated to 95°C for 10 min to denature the exonuclease.

    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 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. .. Amplifications for heavy and light chain were done in separate reactions.

    Molecular Weight:

    Article Title: ConcatSeq: A method for increasing throughput of single molecule sequencing by concatenating short DNA fragments
    Article Snippet: Low molecular weight DNA ladder was purchased from New England BioLabs (N3233). .. Exonuclease III (M0379) and Exonuclease VII (M0206) were purchased from New England BioLabs.

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  • 99
    New England Biolabs exonuclease iii
    Exonuclease Iii, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/exonuclease iii/product/New England Biolabs
    Average 99 stars, based on 21 article reviews
    Price from $9.99 to $1999.99
    exonuclease iii - by Bioz Stars, 2019-07
    99/100 stars
      Buy from Supplier

    97
    New England Biolabs exonuclease vii
    Exonuclease Vii, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/exonuclease vii/product/New England Biolabs
    Average 97 stars, based on 6 article reviews
    Price from $9.99 to $1999.99
    exonuclease vii - by Bioz Stars, 2019-07
    97/100 stars
      Buy from Supplier

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