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Western blot analysis of various lysates using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at 1:1000 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25 µg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 10 s. |
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Western blot analysis of lysates from wild type (WT) and KAT1/HAT1 knockout (KO) HeLa cells using KAT1/HAT1 Rabbit mAb (A4423) at 1:1000 dilution incubated at room temperature for 1.5 hours. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25 µg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 1 s. |
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Immunohistochemistry analysis of paraffin-embedded Human cervix cancer tissue using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate buffer (pH 6.0) prior to IHC staining. |
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Immunohistochemistry analysis of paraffin-embedded Human colon tissue using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate buffer (pH 6.0) prior to IHC staining. |
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Immunohistochemistry analysis of paraffin-embedded Mouse testis tissue using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate buffer (pH 6.0) prior to IHC staining. |
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Immunohistochemistry analysis of paraffin-embedded Rat colon tissue using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate buffer (pH 6.0) prior to IHC staining. |
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Immunofluorescence analysis of C6 cells using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at dilution of 1:100 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) (AS007) at 1:500 dilution. Blue: DAPI for nuclear staining. |
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Immunofluorescence analysis of NIH/3T3 cells using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at dilution of 1:100 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) (AS007) at 1:500 dilution. Blue: DAPI for nuclear staining. |
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Immunoprecipitation of KAT1/HAT1 from 300 µg extracts of MCF7 cells was performed using 2 µg of [KO Validated] KAT1/HAT1 Rabbit mAb (A4423). Rabbit Control IgG (AC005) was used to precipitate the Control IgG sample. IP samples were eluted with 1X Laemmli Buffer. The Input lane represents 10% of the total input. Western blot analysis of immunoprecipitates was conducted using [KO Validated] KAT1/HAT1 Rabbit mAb (A4423) at a dilution of 1:1500. |