quick load purple  (New England Biolabs)


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  • 94
    Name:
    Quick Load Purple 1 kb DNA Ladder
    Description:
    Quick Load Purple 1 kb DNA Ladder 375 gel lanes
    Catalog Number:
    n0552l
    Price:
    129
    Size:
    375 gel lanes
    Category:
    DNA Ladders
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    Structured Review

    New England Biolabs quick load purple
    Quick Load Purple 1 kb DNA Ladder
    Quick Load Purple 1 kb DNA Ladder 375 gel lanes
    https://www.bioz.com/result/quick load purple/product/New England Biolabs
    Average 94 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    quick load purple - by Bioz Stars, 2020-08
    94/100 stars

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    Related Articles

    Marker:

    Article Title: Single-stranded binding proteins and helicase enhance the activity of prokaryotic argonautes in vitro
    Article Snippet: .. The marker ( M ) is NEB® Quick-Load Purple 2-Log DNA Ladder. (PNG) Click here for additional data file. ..

    Article Title: ERIC-PCR technique applied to monitoring and quantification of DNA damage during water disinfection process.
    Article Snippet: .. In this work, we propose a novel application of ERIC-PCR technique to study DNA damage after ultraviolet radiation (UV) and peracetic acid (PAA) treatment for water disinfection purpose. ..

    Polymerase Chain Reaction:

    Article Title: ERIC-PCR technique applied to monitoring and quantification of DNA damage during water disinfection process.
    Article Snippet: .. In this work, we propose a novel application of ERIC-PCR technique to study DNA damage after ultraviolet radiation (UV) and peracetic acid (PAA) treatment for water disinfection purpose. ..

    Synthesized:

    Article Title: ERIC-PCR technique applied to monitoring and quantification of DNA damage during water disinfection process.
    Article Snippet: .. In this work, we propose a novel application of ERIC-PCR technique to study DNA damage after ultraviolet radiation (UV) and peracetic acid (PAA) treatment for water disinfection purpose. ..

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  • 94
    New England Biolabs neb quick load purple
    Tt Ago can cut linearized pUC19 in the presence of ET SSB. Tt Ago is able to cleave linear dsDNA in the presence of ET SSB. pUC19 (2686 bp) was linearized with SspI and used as a substrate for the reaction. Guides pUC19-1 and pUC19-2 (Supporting information S1 Table ) were designed to cut near the BamHI restriction site on pUC19 to generate a 608 bp fragment. Lane 1) <t>NEB</t> Quick-Load Purple 2-Log <t>DNA</t> Ladder (0.1–10.0 kb); 2) Tt Ago + ET SSB; 3) Tt Ago only; 4) SspI linearized pUC19 control.
    Neb Quick Load Purple, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/neb quick load purple/product/New England Biolabs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    neb quick load purple - by Bioz Stars, 2020-08
    94/100 stars
      Buy from Supplier

    92
    New England Biolabs quick load purple
    Tt Ago can cut linearized pUC19 in the presence of ET SSB. Tt Ago is able to cleave linear dsDNA in the presence of ET SSB. pUC19 (2686 bp) was linearized with SspI and used as a substrate for the reaction. Guides pUC19-1 and pUC19-2 (Supporting information S1 Table ) were designed to cut near the BamHI restriction site on pUC19 to generate a 608 bp fragment. Lane 1) <t>NEB</t> Quick-Load Purple 2-Log <t>DNA</t> Ladder (0.1–10.0 kb); 2) Tt Ago + ET SSB; 3) Tt Ago only; 4) SspI linearized pUC19 control.
    Quick Load Purple, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/quick load purple/product/New England Biolabs
    Average 92 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    quick load purple - by Bioz Stars, 2020-08
    92/100 stars
      Buy from Supplier

    94
    New England Biolabs quick load purple 1 kb plus dna ladder
    Tt Ago can cut linearized pUC19 in the presence of ET SSB. Tt Ago is able to cleave linear dsDNA in the presence of ET SSB. pUC19 (2686 bp) was linearized with SspI and used as a substrate for the reaction. Guides pUC19-1 and pUC19-2 (Supporting information S1 Table ) were designed to cut near the BamHI restriction site on pUC19 to generate a 608 bp fragment. Lane 1) <t>NEB</t> Quick-Load Purple 2-Log <t>DNA</t> Ladder (0.1–10.0 kb); 2) Tt Ago + ET SSB; 3) Tt Ago only; 4) SspI linearized pUC19 control.
    Quick Load Purple 1 Kb Plus Dna Ladder, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/quick load purple 1 kb plus dna ladder/product/New England Biolabs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    quick load purple 1 kb plus dna ladder - by Bioz Stars, 2020-08
    94/100 stars
      Buy from Supplier

    Image Search Results


    Tt Ago can cut linearized pUC19 in the presence of ET SSB. Tt Ago is able to cleave linear dsDNA in the presence of ET SSB. pUC19 (2686 bp) was linearized with SspI and used as a substrate for the reaction. Guides pUC19-1 and pUC19-2 (Supporting information S1 Table ) were designed to cut near the BamHI restriction site on pUC19 to generate a 608 bp fragment. Lane 1) NEB Quick-Load Purple 2-Log DNA Ladder (0.1–10.0 kb); 2) Tt Ago + ET SSB; 3) Tt Ago only; 4) SspI linearized pUC19 control.

    Journal: PLoS ONE

    Article Title: Single-stranded binding proteins and helicase enhance the activity of prokaryotic argonautes in vitro

    doi: 10.1371/journal.pone.0203073

    Figure Lengend Snippet: Tt Ago can cut linearized pUC19 in the presence of ET SSB. Tt Ago is able to cleave linear dsDNA in the presence of ET SSB. pUC19 (2686 bp) was linearized with SspI and used as a substrate for the reaction. Guides pUC19-1 and pUC19-2 (Supporting information S1 Table ) were designed to cut near the BamHI restriction site on pUC19 to generate a 608 bp fragment. Lane 1) NEB Quick-Load Purple 2-Log DNA Ladder (0.1–10.0 kb); 2) Tt Ago + ET SSB; 3) Tt Ago only; 4) SspI linearized pUC19 control.

    Article Snippet: The marker ( M ) is NEB® Quick-Load Purple 2-Log DNA Ladder. (PNG) Click here for additional data file.

    Techniques:

    Colony PCR of G. hansenii ATCC 53582 transformed with pSEVA331Bb, pSEVA351, pBla-Vhb-122 and pBAV1K. 1, 2 and 3 – biological replicates of transformed ATCC 53582 used for colony PCR; Pos – Positive control (PCR with pure plasmid DNA), Neg – negative control (colony PCR of untransformed ATCC 53582); L – NEB Quick-Load Purple 2-log DNA ladder. ATCC 53582 were transformed with pSEVA311, pSEVA321, pSEVA331Bb, pSEVA341, pSEVA351, pBla-Vhb-122, pBAV1K, pSB1C3 and pBca1020. Of the used plasmids, colonies were present with pSEVA331Bb, pSEVA351, pBla-Vhb-122 and pBAV1K, and transformants were subsequently confirmed with colony PCR. Although failure to obtain colonies with other plasmids may be due to low transformation efficiencies, we were unable to obtain any transformants with these plasmids in repeat experiments, indicating incompatible origins of replication.

    Journal: Scientific Reports

    Article Title: Genome sequence and plasmid transformation of the model high-yield bacterial cellulose producer Gluconacetobacter hansenii ATCC 53582

    doi: 10.1038/srep23635

    Figure Lengend Snippet: Colony PCR of G. hansenii ATCC 53582 transformed with pSEVA331Bb, pSEVA351, pBla-Vhb-122 and pBAV1K. 1, 2 and 3 – biological replicates of transformed ATCC 53582 used for colony PCR; Pos – Positive control (PCR with pure plasmid DNA), Neg – negative control (colony PCR of untransformed ATCC 53582); L – NEB Quick-Load Purple 2-log DNA ladder. ATCC 53582 were transformed with pSEVA311, pSEVA321, pSEVA331Bb, pSEVA341, pSEVA351, pBla-Vhb-122, pBAV1K, pSB1C3 and pBca1020. Of the used plasmids, colonies were present with pSEVA331Bb, pSEVA351, pBla-Vhb-122 and pBAV1K, and transformants were subsequently confirmed with colony PCR. Although failure to obtain colonies with other plasmids may be due to low transformation efficiencies, we were unable to obtain any transformants with these plasmids in repeat experiments, indicating incompatible origins of replication.

    Article Snippet: The ladder used was NEB Quick-Load Purple 2-log DNA ladder (cat. no. N0550S – NEB) for all tests.

    Techniques: Polymerase Chain Reaction, Transformation Assay, Positive Control, Plasmid Preparation, Negative Control