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α btan20 rat monoclonal dshb btan  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank α btan20 rat monoclonal dshb btan
    α Btan20 Rat Monoclonal Dshb Btan, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 93/100, based on 83 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/α btan20 rat monoclonal dshb btan/product/Developmental Studies Hybridoma Bank
    Average 93 stars, based on 83 article reviews
    α btan20 rat monoclonal dshb btan - by Bioz Stars, 2026-03
    93/100 stars

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    Developmental Studies Hybridoma Bank α btan20 rat monoclonal dshb btan
    α Btan20 Rat Monoclonal Dshb Btan, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Developmental Studies Hybridoma Bank notch1 internal domain btan20
    a , b Western blots for <t>Notch1</t> intracellular domain (NICD) and Rab7 after 72 h of treatment with various concentrations of test compounds in Jurkat ( a ) and Molt-4 cells ( b ). Tubulin is shown as a loading control. Blots are representative of three independent experiments. c Membrane, cytosolic, and whole-cell fractions of Rab7 protein. Western blots are representative of three independent experiments. d Impact of DGBP on NICD expression in other hematopoietic cell lines. Western blots are representative of three independent experiments. e , f Notch1 mRNA expression relative to 18S rRNA. Cells were treated with DGBP alone or a combination with geranylgeranyl diphosphate (GGPP) for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control
    Notch1 Internal Domain Btan20, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Developmental Studies Hybridoma Bank notch 1 btan20 antibody
    a , b Western blots for <t>Notch1</t> intracellular domain (NICD) and Rab7 after 72 h of treatment with various concentrations of test compounds in Jurkat ( a ) and Molt-4 cells ( b ). Tubulin is shown as a loading control. Blots are representative of three independent experiments. c Membrane, cytosolic, and whole-cell fractions of Rab7 protein. Western blots are representative of three independent experiments. d Impact of DGBP on NICD expression in other hematopoietic cell lines. Western blots are representative of three independent experiments. e , f Notch1 mRNA expression relative to 18S rRNA. Cells were treated with DGBP alone or a combination with geranylgeranyl diphosphate (GGPP) for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control
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    Developmental Studies Hybridoma Bank btan20 notch1
    a , b Western blots for <t>Notch1</t> intracellular domain (NICD) and Rab7 after 72 h of treatment with various concentrations of test compounds in Jurkat ( a ) and Molt-4 cells ( b ). Tubulin is shown as a loading control. Blots are representative of three independent experiments. c Membrane, cytosolic, and whole-cell fractions of Rab7 protein. Western blots are representative of three independent experiments. d Impact of DGBP on NICD expression in other hematopoietic cell lines. Western blots are representative of three independent experiments. e , f Notch1 mRNA expression relative to 18S rRNA. Cells were treated with DGBP alone or a combination with geranylgeranyl diphosphate (GGPP) for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control
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    Developmental Studies Hybridoma Bank btan20
    a , b Western blots for <t>Notch1</t> intracellular domain (NICD) and Rab7 after 72 h of treatment with various concentrations of test compounds in Jurkat ( a ) and Molt-4 cells ( b ). Tubulin is shown as a loading control. Blots are representative of three independent experiments. c Membrane, cytosolic, and whole-cell fractions of Rab7 protein. Western blots are representative of three independent experiments. d Impact of DGBP on NICD expression in other hematopoietic cell lines. Western blots are representative of three independent experiments. e , f Notch1 mRNA expression relative to 18S rRNA. Cells were treated with DGBP alone or a combination with geranylgeranyl diphosphate (GGPP) for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control
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    Developmental Studies Hybridoma Bank notch1 btan20
    a , b Western blots for <t>Notch1</t> intracellular domain (NICD) and Rab7 after 72 h of treatment with various concentrations of test compounds in Jurkat ( a ) and Molt-4 cells ( b ). Tubulin is shown as a loading control. Blots are representative of three independent experiments. c Membrane, cytosolic, and whole-cell fractions of Rab7 protein. Western blots are representative of three independent experiments. d Impact of DGBP on NICD expression in other hematopoietic cell lines. Western blots are representative of three independent experiments. e , f Notch1 mRNA expression relative to 18S rRNA. Cells were treated with DGBP alone or a combination with geranylgeranyl diphosphate (GGPP) for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control
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    a , b Western blots for Notch1 intracellular domain (NICD) and Rab7 after 72 h of treatment with various concentrations of test compounds in Jurkat ( a ) and Molt-4 cells ( b ). Tubulin is shown as a loading control. Blots are representative of three independent experiments. c Membrane, cytosolic, and whole-cell fractions of Rab7 protein. Western blots are representative of three independent experiments. d Impact of DGBP on NICD expression in other hematopoietic cell lines. Western blots are representative of three independent experiments. e , f Notch1 mRNA expression relative to 18S rRNA. Cells were treated with DGBP alone or a combination with geranylgeranyl diphosphate (GGPP) for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control

    Journal: Cell Death & Disease

    Article Title: Regulation of the Notch-ATM-abl axis by geranylgeranyl diphosphate synthase inhibition

    doi: 10.1038/s41419-019-1973-7

    Figure Lengend Snippet: a , b Western blots for Notch1 intracellular domain (NICD) and Rab7 after 72 h of treatment with various concentrations of test compounds in Jurkat ( a ) and Molt-4 cells ( b ). Tubulin is shown as a loading control. Blots are representative of three independent experiments. c Membrane, cytosolic, and whole-cell fractions of Rab7 protein. Western blots are representative of three independent experiments. d Impact of DGBP on NICD expression in other hematopoietic cell lines. Western blots are representative of three independent experiments. e , f Notch1 mRNA expression relative to 18S rRNA. Cells were treated with DGBP alone or a combination with geranylgeranyl diphosphate (GGPP) for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control

    Article Snippet: The antibody for the Notch1 internal domain (bTAN20) was purchased from the Developmental Studies Hybridoma Bank (deposited by Artavanis-Tsakonas ).

    Techniques: Western Blot, Control, Membrane, Expressing

    a , b Annexin V staining of Molt-4 or Jurkat cells treated with DGBP and co-treated with or without ( a ) DAPT or ( b ) MK-0752 for 72 h. Graphs represent means and standard deviations of three independent experiments. Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus untreated controls. ‡ p < 0.05 versus DGBP-treated condition. c , d Western blot of full-length Notch1 and NICD in Molt-4 cells following 72 h of treatment with DGBP and co-treatment with or without either the GGDPS product GGPP ( c ) or the caspase inhibitor Z-VAD-FMK ( d ). Tubulin is shown as a loading control. e , f Western blots of Notch1 and NICD after 72 h of treatment with DGBP and co-treatment with or without DAPT in Molt-4 ( e ) and Jurkat ( f ) cells. All Western blots are representative of three independent experiments

    Journal: Cell Death & Disease

    Article Title: Regulation of the Notch-ATM-abl axis by geranylgeranyl diphosphate synthase inhibition

    doi: 10.1038/s41419-019-1973-7

    Figure Lengend Snippet: a , b Annexin V staining of Molt-4 or Jurkat cells treated with DGBP and co-treated with or without ( a ) DAPT or ( b ) MK-0752 for 72 h. Graphs represent means and standard deviations of three independent experiments. Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus untreated controls. ‡ p < 0.05 versus DGBP-treated condition. c , d Western blot of full-length Notch1 and NICD in Molt-4 cells following 72 h of treatment with DGBP and co-treatment with or without either the GGDPS product GGPP ( c ) or the caspase inhibitor Z-VAD-FMK ( d ). Tubulin is shown as a loading control. e , f Western blots of Notch1 and NICD after 72 h of treatment with DGBP and co-treatment with or without DAPT in Molt-4 ( e ) and Jurkat ( f ) cells. All Western blots are representative of three independent experiments

    Article Snippet: The antibody for the Notch1 internal domain (bTAN20) was purchased from the Developmental Studies Hybridoma Bank (deposited by Artavanis-Tsakonas ).

    Techniques: Staining, Western Blot, Control

    a Notch1 mRNA expression relative to 18S rRNA. Jurkat cells were treated with inhibitor alone or combinations for 72 h. b Luciferase activity in Jurkat cells transfected with Notch1 3′UTR. Cells were treated with inhibitor alone or co-treated with DGBP for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control. ‡ p < 0.05 versus DGBP-treated condition

    Journal: Cell Death & Disease

    Article Title: Regulation of the Notch-ATM-abl axis by geranylgeranyl diphosphate synthase inhibition

    doi: 10.1038/s41419-019-1973-7

    Figure Lengend Snippet: a Notch1 mRNA expression relative to 18S rRNA. Jurkat cells were treated with inhibitor alone or combinations for 72 h. b Luciferase activity in Jurkat cells transfected with Notch1 3′UTR. Cells were treated with inhibitor alone or co-treated with DGBP for 72 h. In all graphs, the bars represent means and standard deviations of three independent experiments ( n = 3). Statistical significance was determined by two-way ANOVA with Tukey’s post hoc analysis. * p < 0.05 versus the corresponding control. ‡ p < 0.05 versus DGBP-treated condition

    Article Snippet: The antibody for the Notch1 internal domain (bTAN20) was purchased from the Developmental Studies Hybridoma Bank (deposited by Artavanis-Tsakonas ).

    Techniques: Expressing, Luciferase, Activity Assay, Transfection, Control