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signal immunoreaction enhancer solution 2  (Toyobo)


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    Structured Review

    Toyobo signal immunoreaction enhancer solution 2
    Signal Immunoreaction Enhancer Solution 2, supplied by Toyobo, used in various techniques. Bioz Stars score: 98/100, based on 3785 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/signal+immunoreaction+enhancer+solution/Can+Get+Signal/pmc13107096-50-30-36
    Average 98 stars, based on 3785 article reviews
    signal immunoreaction enhancer solution 2 - by Bioz Stars, 2026-10
    98/100 stars

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    Incubation:

    Article Title: Proteomic analysis revealed the potential usefulness of faecal extracellular vesicles in colorectal cancer diagnosis
    Article Snippet: .. The primary antibody was diluted using Can Get Signal Immunoreaction Enhancer Solution (TOYOBO) and incubated overnight at 4 °C. .. After washing, the membrane was incubated with a secondary antibody, horseradish peroxidase-labelled anti-rabbit immunoglobulin G (Cell Signalling Technology).

    Article Title: Wnt10a exhibit spatiotemporal singularity in the temporal changes of angiogenesis in regenerated pulp-like tissue
    Article Snippet: After transcription, anti-Wnt10a antibody (1:500) (NBP1-76,916, Novus Biologicals, CO, USA), anti-VEGF antibody (1:1000) (19,003–1-AP, Proteintech, Chicago, IL, USA),and anti-Tie-2 antibody (1:1000) (19,157–1-AP, Proteintech, Chicago, IL, USA) were used as primary antibodies using the iBind Flex Western System (Thermo Fisher Scientific, Waltham, MA, USA). .. Rabbit IgG antibody (1:5000) (SA00001-2, Proteintech, Chicago, IL, USA) was diluted in Can Get Signal® Immunoreaction Enhancer Solution (Toyobo, Osaka, Japan) and incubated for 16 h as the secondary antibody. .. The samples were then used with SuperSignalTM West Pico PLUS Chemiluminescent Substrate (Thermo Fisher Scientific, Waltham, MA, USA) and detected with the Chemi DocTM Touch MP Imaging System (Bio- Rad Laboratories, Hercules, CA, USA).

    Article Title: Proximity Labelling‐Based Proteomics Identifies Antiviral Host Factors Associated With the Potexvirus Replicase
    Article Snippet: Protein extracts from co‐immunoprecipitation, chemical treatment, or proximity labelling experiment were mixed with equal volumes of 2 × SDS sample buffer (Bio‐Rad) containing 5% v/v 3‐mercapto‐1,2‐propanediol and incubated for 5 min at 95°C. .. Samples were separated on 12.5% SDS‐PAGE gels (ATTO) and transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore) using the wet transfer method at 500 mA, 100 V for 1 h. Membranes were blocked with Blocking One (NACALAI TESQUE) for 1 h at room temperature, washed with phosphate‐buffered saline containing 1% Tween‐20 (PBS‐T), and then incubated with antibody solutions prepared in Can Get Signal Immunoreaction Enhancer Solution (Toyobo). .. For detection of myc‐tagged proteins, mouse anti‐Myc tag antibody (Merck Millipore, clone 4A6; 1:1000 dilution) and horseradish peroxidase (HRP)‐conjugated goat anti‐mouse IgG (32430) (Thermo Fisher Scientific, #32430; 1:2000) were used.

    Article Title: The effect of SIRT1 knockdown on the gene expression of CoQ10 biosynthetic enzymes
    Article Snippet: .. The membranes were blocked with 5% skimmed milk in TBST for 1 h at room temperature, followed by incubation with COQ6 Antibody (H-1) (sc-393932; Santa Cruz Biotechnology, Dallas, TX) diluted in Can Get Signal immunoreaction enhancer solution (Toyobo, Osaka, Japan) 1:500 for 1.5 h at room temperature. ..

    Article Title: Discovery of a Novel γ-Glutamylcyclotransferase Inhibitor Plumbagin by Luminescence-Based High-Throughput Screening.
    Article Snippet: .. Membranes were blocked with 3% or 5% fat- free dry milk or 3% bovine serum albumin in TBS with 0.1% Tween- 20, or Blocking Reagent for Can Get Signal (TOYOBO, Osaka, Japan), and then incubated with the indicated primary and secondary antibodies in Signal Enhancer HIKARI (Nacalai Tesque), Can Get Signal Immunoreaction Enhancer Solution (TOYOBO). .. The target proteins were visualized by the Immobilon Western Chemiluminescent HRP Substrate (Millipore, Burlington, MA), Chemi- Lumi One L/Super (Nacalai Tesque), or Clarity Western ECL Substrate (Bio- Rad).

    Article Title: Wnt10a exhibit spatiotemporal singularity in the temporal changes of angiogenesis in regenerated pulp-like tissue.
    Article Snippet: After transcription, anti-Wnt10a antibody (1:500) (NBP1-76,916, Novus Biologicals, CO, USA), anti-VEGF antibody (1:1000) (19,003–1-AP, Proteintech, Chicago, IL, USA),and anti-Tie-2 antibody (1:1000) (19,157–1-AP, Proteintech, Chicago, IL, USA) were used as primary antibodies using the iBind Flex Western System (Thermo Fisher Scientific, Waltham, MA, USA). .. Rabbit IgG antibody (1:5000) (SA00001-2, Proteintech, Chicago, IL, USA) was diluted in Can Get Signal® Immunoreaction Enhancer Solution (Toyobo, Osaka, Japan) and incubated for 16 h as the secondary antibody. .. The samples were then used with SuperSignalTM West Pico PLUS Chemiluminescent Substrate (Thermo Fisher Scientific, Waltham, MA, USA) and detected with the Chemi DocTM Touch MP Imaging System (Bio- Rad Laboratories, Hercules, CA, USA).

    Article Title: Proximity Labelling-Based Proteomics Identifies Antiviral Host Factors Associated With the Potexvirus Replicase.
    Article Snippet: Protein extracts from co- immunoprecipitation, chemical treatment, or proximity labelling experiment were mixed with equal volumes of 2 × SDS sample buffer (Bio- Rad) containing 5% v/v 3- mercapto- 1,2- propanediol and incubated for 5 min at 95°C. .. Samples were separated on 12.5% SDS- PAGE gels (ATTO) and transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore) using the wet transfer method at 500 mA, 100 V for 1 h. Membranes were blocked with Blocking One (NACALAI TESQUE) for 1 h at room temperature, washed with phosphate- buffered saline containing 1% Tween- 20 (PBS- T), and then incubated with antibody solutions prepared in Can Get Signal Immunoreaction Enhancer Solution (Toyobo). .. For detection of myc- tagged proteins, mouse anti- Myc tag antibody (Merck Millipore, clone 4A6; 1:1000 dilution) and horseradish peroxidase (HRP)- conjugated goat anti- mouse IgG (32430) (Thermo Fisher Scientific, #32430; 1:2000) were used.

    Blocking Assay:

    Article Title: Proximity Labelling‐Based Proteomics Identifies Antiviral Host Factors Associated With the Potexvirus Replicase
    Article Snippet: Protein extracts from co‐immunoprecipitation, chemical treatment, or proximity labelling experiment were mixed with equal volumes of 2 × SDS sample buffer (Bio‐Rad) containing 5% v/v 3‐mercapto‐1,2‐propanediol and incubated for 5 min at 95°C. .. Samples were separated on 12.5% SDS‐PAGE gels (ATTO) and transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore) using the wet transfer method at 500 mA, 100 V for 1 h. Membranes were blocked with Blocking One (NACALAI TESQUE) for 1 h at room temperature, washed with phosphate‐buffered saline containing 1% Tween‐20 (PBS‐T), and then incubated with antibody solutions prepared in Can Get Signal Immunoreaction Enhancer Solution (Toyobo). .. For detection of myc‐tagged proteins, mouse anti‐Myc tag antibody (Merck Millipore, clone 4A6; 1:1000 dilution) and horseradish peroxidase (HRP)‐conjugated goat anti‐mouse IgG (32430) (Thermo Fisher Scientific, #32430; 1:2000) were used.

    Article Title: Discovery of a Novel γ-Glutamylcyclotransferase Inhibitor Plumbagin by Luminescence-Based High-Throughput Screening.
    Article Snippet: .. Membranes were blocked with 3% or 5% fat- free dry milk or 3% bovine serum albumin in TBS with 0.1% Tween- 20, or Blocking Reagent for Can Get Signal (TOYOBO, Osaka, Japan), and then incubated with the indicated primary and secondary antibodies in Signal Enhancer HIKARI (Nacalai Tesque), Can Get Signal Immunoreaction Enhancer Solution (TOYOBO). .. The target proteins were visualized by the Immobilon Western Chemiluminescent HRP Substrate (Millipore, Burlington, MA), Chemi- Lumi One L/Super (Nacalai Tesque), or Clarity Western ECL Substrate (Bio- Rad).

    Article Title: Proximity Labelling-Based Proteomics Identifies Antiviral Host Factors Associated With the Potexvirus Replicase.
    Article Snippet: Protein extracts from co- immunoprecipitation, chemical treatment, or proximity labelling experiment were mixed with equal volumes of 2 × SDS sample buffer (Bio- Rad) containing 5% v/v 3- mercapto- 1,2- propanediol and incubated for 5 min at 95°C. .. Samples were separated on 12.5% SDS- PAGE gels (ATTO) and transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore) using the wet transfer method at 500 mA, 100 V for 1 h. Membranes were blocked with Blocking One (NACALAI TESQUE) for 1 h at room temperature, washed with phosphate- buffered saline containing 1% Tween- 20 (PBS- T), and then incubated with antibody solutions prepared in Can Get Signal Immunoreaction Enhancer Solution (Toyobo). .. For detection of myc- tagged proteins, mouse anti- Myc tag antibody (Merck Millipore, clone 4A6; 1:1000 dilution) and horseradish peroxidase (HRP)- conjugated goat anti- mouse IgG (32430) (Thermo Fisher Scientific, #32430; 1:2000) were used.

    Article Title: Method for purifying protein derived from membrane protein complex
    Article Snippet: After the transfer, the PVDF membrane was washed with PBS- and then blocked overnight at 4° C. using PVDF Blocking Reagent for Can Get Signal (TOYOBO). .. After the blocking, the PVDF membrane was washed with PBS-T and then impregnated with a mixture of 5 mL of Solution 1 for primary antibody of Can Get Signal Immunoreaction Enhancer Solution (TOYOBO) with 2.5 μL of a 1 mg/mL HRT-antibody solution (2000-fold dilution) for 10 minutes at room temperature to perform a primary antibody reaction. ..

    Saline:

    Article Title: Proximity Labelling‐Based Proteomics Identifies Antiviral Host Factors Associated With the Potexvirus Replicase
    Article Snippet: Protein extracts from co‐immunoprecipitation, chemical treatment, or proximity labelling experiment were mixed with equal volumes of 2 × SDS sample buffer (Bio‐Rad) containing 5% v/v 3‐mercapto‐1,2‐propanediol and incubated for 5 min at 95°C. .. Samples were separated on 12.5% SDS‐PAGE gels (ATTO) and transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore) using the wet transfer method at 500 mA, 100 V for 1 h. Membranes were blocked with Blocking One (NACALAI TESQUE) for 1 h at room temperature, washed with phosphate‐buffered saline containing 1% Tween‐20 (PBS‐T), and then incubated with antibody solutions prepared in Can Get Signal Immunoreaction Enhancer Solution (Toyobo). .. For detection of myc‐tagged proteins, mouse anti‐Myc tag antibody (Merck Millipore, clone 4A6; 1:1000 dilution) and horseradish peroxidase (HRP)‐conjugated goat anti‐mouse IgG (32430) (Thermo Fisher Scientific, #32430; 1:2000) were used.

    Article Title: Proximity Labelling-Based Proteomics Identifies Antiviral Host Factors Associated With the Potexvirus Replicase.
    Article Snippet: Protein extracts from co- immunoprecipitation, chemical treatment, or proximity labelling experiment were mixed with equal volumes of 2 × SDS sample buffer (Bio- Rad) containing 5% v/v 3- mercapto- 1,2- propanediol and incubated for 5 min at 95°C. .. Samples were separated on 12.5% SDS- PAGE gels (ATTO) and transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore) using the wet transfer method at 500 mA, 100 V for 1 h. Membranes were blocked with Blocking One (NACALAI TESQUE) for 1 h at room temperature, washed with phosphate- buffered saline containing 1% Tween- 20 (PBS- T), and then incubated with antibody solutions prepared in Can Get Signal Immunoreaction Enhancer Solution (Toyobo). .. For detection of myc- tagged proteins, mouse anti- Myc tag antibody (Merck Millipore, clone 4A6; 1:1000 dilution) and horseradish peroxidase (HRP)- conjugated goat anti- mouse IgG (32430) (Thermo Fisher Scientific, #32430; 1:2000) were used.

    SDS Page:

    Article Title: Proximity Labelling-Based Proteomics Identifies Antiviral Host Factors Associated With the Potexvirus Replicase.
    Article Snippet: Protein extracts from co- immunoprecipitation, chemical treatment, or proximity labelling experiment were mixed with equal volumes of 2 × SDS sample buffer (Bio- Rad) containing 5% v/v 3- mercapto- 1,2- propanediol and incubated for 5 min at 95°C. .. Samples were separated on 12.5% SDS- PAGE gels (ATTO) and transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore) using the wet transfer method at 500 mA, 100 V for 1 h. Membranes were blocked with Blocking One (NACALAI TESQUE) for 1 h at room temperature, washed with phosphate- buffered saline containing 1% Tween- 20 (PBS- T), and then incubated with antibody solutions prepared in Can Get Signal Immunoreaction Enhancer Solution (Toyobo). .. For detection of myc- tagged proteins, mouse anti- Myc tag antibody (Merck Millipore, clone 4A6; 1:1000 dilution) and horseradish peroxidase (HRP)- conjugated goat anti- mouse IgG (32430) (Thermo Fisher Scientific, #32430; 1:2000) were used.

    Membrane:

    Article Title: Method for purifying protein derived from membrane protein complex
    Article Snippet: After the transfer, the PVDF membrane was washed with PBS- and then blocked overnight at 4° C. using PVDF Blocking Reagent for Can Get Signal (TOYOBO). .. After the blocking, the PVDF membrane was washed with PBS-T and then impregnated with a mixture of 5 mL of Solution 1 for primary antibody of Can Get Signal Immunoreaction Enhancer Solution (TOYOBO) with 2.5 μL of a 1 mg/mL HRT-antibody solution (2000-fold dilution) for 10 minutes at room temperature to perform a primary antibody reaction. ..



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