proteinase k Promega Search Results


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  • 99
    New England Biolabs proteinase k
    Proteinase K, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 3211 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega proteinase k
    Comparison of anti-wilt activity of the fractions obtained by exclusion chromatography of high-molecular weight metabolites from  F. oxysporum  strain CS-20.  Seedlings were inoculated by immersion in a suspension with a final concentration of 10 6  spores/ml, containing spores of two pathogenic strains F37 and Fot3 (1:1). Disease symptoms were examined at 15  (A) , and 21  (B)  days after inoculation of tomato seedlings, which roots were pre-exposed to intact (dark gray columns) or proteinase K-treated (light gray columns) fractions eluted as peaks III, IV, and V. Inoculated seedlings non-exposed to the fractions are referred to as infected control (IfCtrl, black columns). Histograms represent values of average disease index from two independent experiments of each treatment done in triplicate. Bars represent SD.
    Proteinase K, supplied by Promega, used in various techniques. Bioz Stars score: 95/100, based on 3010 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega proteinase k promega treatment
    Comparison of anti-wilt activity of the fractions obtained by exclusion chromatography of high-molecular weight metabolites from  F. oxysporum  strain CS-20.  Seedlings were inoculated by immersion in a suspension with a final concentration of 10 6  spores/ml, containing spores of two pathogenic strains F37 and Fot3 (1:1). Disease symptoms were examined at 15  (A) , and 21  (B)  days after inoculation of tomato seedlings, which roots were pre-exposed to intact (dark gray columns) or proteinase K-treated (light gray columns) fractions eluted as peaks III, IV, and V. Inoculated seedlings non-exposed to the fractions are referred to as infected control (IfCtrl, black columns). Histograms represent values of average disease index from two independent experiments of each treatment done in triplicate. Bars represent SD.
    Proteinase K Promega Treatment, supplied by Promega, used in various techniques. Bioz Stars score: 88/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Promega nacl proteinase k
    Comparison of anti-wilt activity of the fractions obtained by exclusion chromatography of high-molecular weight metabolites from  F. oxysporum  strain CS-20.  Seedlings were inoculated by immersion in a suspension with a final concentration of 10 6  spores/ml, containing spores of two pathogenic strains F37 and Fot3 (1:1). Disease symptoms were examined at 15  (A) , and 21  (B)  days after inoculation of tomato seedlings, which roots were pre-exposed to intact (dark gray columns) or proteinase K-treated (light gray columns) fractions eluted as peaks III, IV, and V. Inoculated seedlings non-exposed to the fractions are referred to as infected control (IfCtrl, black columns). Histograms represent values of average disease index from two independent experiments of each treatment done in triplicate. Bars represent SD.
    Nacl Proteinase K, supplied by Promega, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Promega proteinase k buffer
    ( A ) Schematic depicting PCR genotyping assay. The number 104 denotes primer oMT104, common to both alleles; 103 denotes oMT103, specific to the wild-type allele; 106 denotes oMT106, specific to the mutant allele. ( B ) PCR genotyping of 3.5 dpc embryos (blastocysts or late morulae) derived from heterozygous crosses. Embryos were digested individually with <t>proteinase</t> K and subjected to PCR as detailed in Materials and Methods. Control reaction contained media alone. Wild-type, heterozygous, and homozygous mutant embryos were found in Mendelian ratios.
    Proteinase K Buffer, supplied by Promega, used in various techniques. Bioz Stars score: 91/100, based on 66 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    Promega proteinase k incubation
    ( A ) Schematic depicting PCR genotyping assay. The number 104 denotes primer oMT104, common to both alleles; 103 denotes oMT103, specific to the wild-type allele; 106 denotes oMT106, specific to the mutant allele. ( B ) PCR genotyping of 3.5 dpc embryos (blastocysts or late morulae) derived from heterozygous crosses. Embryos were digested individually with <t>proteinase</t> K and subjected to PCR as detailed in Materials and Methods. Control reaction contained media alone. Wild-type, heterozygous, and homozygous mutant embryos were found in Mendelian ratios.
    Proteinase K Incubation, supplied by Promega, used in various techniques. Bioz Stars score: 93/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Promega proteinase k solution
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Proteinase K Solution, supplied by Promega, used in various techniques. Bioz Stars score: 92/100, based on 99 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Promega proteinase k rq1 dnase
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Proteinase K Rq1 Dnase, supplied by Promega, used in various techniques. Bioz Stars score: 85/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega sodium dodecyl sulphate proteinase k treatment
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Sodium Dodecyl Sulphate Proteinase K Treatment, supplied by Promega, used in various techniques. Bioz Stars score: 88/100, based on 81 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega sodium dodecyl sulfate proteinase k treatment
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Sodium Dodecyl Sulfate Proteinase K Treatment, supplied by Promega, used in various techniques. Bioz Stars score: 88/100, based on 28 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega standard sodium dodecyl sulphate proteinase k treatment
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Standard Sodium Dodecyl Sulphate Proteinase K Treatment, supplied by Promega, used in various techniques. Bioz Stars score: 85/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega proteinase k wizard dna clean up system
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Proteinase K Wizard Dna Clean Up System, supplied by Promega, used in various techniques. Bioz Stars score: 99/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega lysis buffer
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Lysis Buffer, supplied by Promega, used in various techniques. Bioz Stars score: 99/100, based on 12356 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega extraction buffer
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Extraction Buffer, supplied by Promega, used in various techniques. Bioz Stars score: 99/100, based on 200 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega wizard dna extraction kit
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Wizard Dna Extraction Kit, supplied by Promega, used in various techniques. Bioz Stars score: 94/100, based on 276 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega dna purification kit
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Dna Purification Kit, supplied by Promega, used in various techniques. Bioz Stars score: 96/100, based on 1187 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega wizard genomic dna purification standard protocol
    GCase inhibition caused accumulation of <t>proteinase-K-resistant</t> insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble
    Wizard Genomic Dna Purification Standard Protocol, supplied by Promega, used in various techniques. Bioz Stars score: 85/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Comparison of anti-wilt activity of the fractions obtained by exclusion chromatography of high-molecular weight metabolites from  F. oxysporum  strain CS-20.  Seedlings were inoculated by immersion in a suspension with a final concentration of 10 6  spores/ml, containing spores of two pathogenic strains F37 and Fot3 (1:1). Disease symptoms were examined at 15  (A) , and 21  (B)  days after inoculation of tomato seedlings, which roots were pre-exposed to intact (dark gray columns) or proteinase K-treated (light gray columns) fractions eluted as peaks III, IV, and V. Inoculated seedlings non-exposed to the fractions are referred to as infected control (IfCtrl, black columns). Histograms represent values of average disease index from two independent experiments of each treatment done in triplicate. Bars represent SD.

    Journal: Frontiers in Plant Science

    Article Title: Identification of a Novel Small Cysteine-Rich Protein in the Fraction from the Biocontrol Fusarium oxysporum Strain CS-20 that Mitigates Fusarium Wilt Symptoms and Triggers Defense Responses in Tomato

    doi: 10.3389/fpls.2015.01207

    Figure Lengend Snippet: Comparison of anti-wilt activity of the fractions obtained by exclusion chromatography of high-molecular weight metabolites from F. oxysporum strain CS-20. Seedlings were inoculated by immersion in a suspension with a final concentration of 10 6 spores/ml, containing spores of two pathogenic strains F37 and Fot3 (1:1). Disease symptoms were examined at 15 (A) , and 21 (B) days after inoculation of tomato seedlings, which roots were pre-exposed to intact (dark gray columns) or proteinase K-treated (light gray columns) fractions eluted as peaks III, IV, and V. Inoculated seedlings non-exposed to the fractions are referred to as infected control (IfCtrl, black columns). Histograms represent values of average disease index from two independent experiments of each treatment done in triplicate. Bars represent SD.

    Article Snippet: Protein Digestion Assay Samples of the protein-containing fractions isolated by size-exclusion chromatography were treated with proteinase K (Promega, USA) following a protocol recommended by the manufacturer for native protein cleavage .

    Techniques: Activity Assay, Chromatography, Molecular Weight, Concentration Assay, Infection

    Alkalinization of the incubation medium by cultured tomato cells in response to CS-20 proteins contained in fraction V, which reduced Fusarium wilt severity in tomato seedlings. (A) Profiles of extracellular pH change in suspensions of two cell lines after addition of the lyophilized fraction V to a final concentration of 10 μg/ml. Cell response (line β) to the fraction pretreated with proteinase K shown by dotted line. The solid line shows extracellular pH of non-treated cells. (B) Dose-rate effect of the fraction V isolated from CS-20 on tomato cell line γ. Numerals near curves show final concentrations (μg per ml) of the lyophilized fraction V in the tomato cell suspension. Re-stimulation of the reversible response is exemplified for a concentration of 2.5 μg/ml. Dotted line illustrates the irreversibility of alkalinization response to preparation from the pathogenic FOL (strain F37), obtained by the same procedures that were applied to isolate fraction V from CS-20. (C) The extracellular pH values after addition of inactive fractions III (white circles) or IV (white triangles) at a concentration of 10 μg/ml. Asterisks show extracellular pH of non-treated cells. Arrows indicated starting point of treatments. The representative data are out of one of three experiments with the protein fraction V samples independently isolated from CS-20 culture.

    Journal: Frontiers in Plant Science

    Article Title: Identification of a Novel Small Cysteine-Rich Protein in the Fraction from the Biocontrol Fusarium oxysporum Strain CS-20 that Mitigates Fusarium Wilt Symptoms and Triggers Defense Responses in Tomato

    doi: 10.3389/fpls.2015.01207

    Figure Lengend Snippet: Alkalinization of the incubation medium by cultured tomato cells in response to CS-20 proteins contained in fraction V, which reduced Fusarium wilt severity in tomato seedlings. (A) Profiles of extracellular pH change in suspensions of two cell lines after addition of the lyophilized fraction V to a final concentration of 10 μg/ml. Cell response (line β) to the fraction pretreated with proteinase K shown by dotted line. The solid line shows extracellular pH of non-treated cells. (B) Dose-rate effect of the fraction V isolated from CS-20 on tomato cell line γ. Numerals near curves show final concentrations (μg per ml) of the lyophilized fraction V in the tomato cell suspension. Re-stimulation of the reversible response is exemplified for a concentration of 2.5 μg/ml. Dotted line illustrates the irreversibility of alkalinization response to preparation from the pathogenic FOL (strain F37), obtained by the same procedures that were applied to isolate fraction V from CS-20. (C) The extracellular pH values after addition of inactive fractions III (white circles) or IV (white triangles) at a concentration of 10 μg/ml. Asterisks show extracellular pH of non-treated cells. Arrows indicated starting point of treatments. The representative data are out of one of three experiments with the protein fraction V samples independently isolated from CS-20 culture.

    Article Snippet: Protein Digestion Assay Samples of the protein-containing fractions isolated by size-exclusion chromatography were treated with proteinase K (Promega, USA) following a protocol recommended by the manufacturer for native protein cleavage .

    Techniques: Incubation, Cell Culture, Concentration Assay, Isolation

    ( A ) Schematic depicting PCR genotyping assay. The number 104 denotes primer oMT104, common to both alleles; 103 denotes oMT103, specific to the wild-type allele; 106 denotes oMT106, specific to the mutant allele. ( B ) PCR genotyping of 3.5 dpc embryos (blastocysts or late morulae) derived from heterozygous crosses. Embryos were digested individually with proteinase K and subjected to PCR as detailed in Materials and Methods. Control reaction contained media alone. Wild-type, heterozygous, and homozygous mutant embryos were found in Mendelian ratios.

    Journal: Genes & Development

    Article Title: Ubiquitous expression and embryonic requirement for RNA polymerase II coactivator subunit Srb7 in mice

    doi:

    Figure Lengend Snippet: ( A ) Schematic depicting PCR genotyping assay. The number 104 denotes primer oMT104, common to both alleles; 103 denotes oMT103, specific to the wild-type allele; 106 denotes oMT106, specific to the mutant allele. ( B ) PCR genotyping of 3.5 dpc embryos (blastocysts or late morulae) derived from heterozygous crosses. Embryos were digested individually with proteinase K and subjected to PCR as detailed in Materials and Methods. Control reaction contained media alone. Wild-type, heterozygous, and homozygous mutant embryos were found in Mendelian ratios.

    Article Snippet: To genotype embryos, heterozygotes were mated, embryos were collected and developmental stage noted, and were placed in 0.2-ml PCR tubes with 5 μl of proteinase K buffer (1× Promega Mg-free PCR buffer + 200 μg/ml proteinase K).

    Techniques: Polymerase Chain Reaction, Genotyping Assay, Mutagenesis, Derivative Assay

    GCase inhibition caused accumulation of proteinase-K-resistant insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble

    Journal: Antioxidants & Redox Signaling

    Article Title: Sustained Systemic Glucocerebrosidase Inhibition Induces Brain α-Synuclein Aggregation, Microglia and Complement C1q Activation in Mice

    doi: 10.1089/ars.2015.6307

    Figure Lengend Snippet: GCase inhibition caused accumulation of proteinase-K-resistant insoluble α -synuclein aggregates and induced autophagy–lysosomal proteins in the nigrostriatal pathway. Mice were treated with either vehicle or CBE and immunostained for insoluble

    Article Snippet: To visualize insoluble α-synuclein aggregates, tissue sections were premounted on gelatin-coated slides and incubated with proteinase-K solution (10 μg/ml; Promega) for 20–30 min at 37°C.

    Techniques: Inhibition, Mouse Assay