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Western blot analysis of various lysates, using SNRPA1 Rabbit mAb (A0647) at 1:1000 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25µg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 3s. |
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Immunohistochemistry analysis of paraffin-embeddedHuman liver tissue usingSNRPA1 Rabbit mAb(A0647) at a dilution of 1:200 (40x lens).High pressure antigen retrieval was performed with 0.01 M citrate buffer (pH 6.0) prior to IHC staining. |
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Immunohistochemistry analysis of paraffin-embeddedHuman esophagus tissue usingSNRPA1 Rabbit mAb(A0647) at a dilution of 1:200 (40x lens).High pressure antigen retrieval was performed with 0.01 M citrate buffer (pH 6.0) prior to IHC staining. |
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Immunohistochemistry analysis of paraffin-embeddedMouse intestin tissue usingSNRPA1 Rabbit mAb(A0647) at a dilution of 1:200 (40x lens).High pressure antigen retrieval was performed with 0.01 M citrate buffer (pH 6.0) prior to IHC staining. |
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Immunohistochemistry analysis of paraffin-embeddedHuman thyroid tissue usingSNRPA1 Rabbit mAb(A0647) at a dilution of 1:200 (40x lens).High pressure antigen retrieval was performed with 0.01 M citrate buffer (pH 6.0) prior to IHC staining. |
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Immunohistochemistry analysis of paraffin-embeddedRat intestine tissue usingSNRPA1 Rabbit mAb(A0647) at a dilution of 1:200 (40x lens).High pressure antigen retrieval was performed with 0.01 M citrate buffer (pH 6.0) prior to IHC staining. |
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Immunoprecipitation of SNRPA1 from 300 µg extracts of Hep G2 cells was performed using 3 µg of SNRPA1 Rabbit mAb (A0647). Rabbit Control IgG (AC005) was used to precipitate the Control IgG sample. IP samples were eluted with 1* Laemmli Buffer. The Input lane represents 10% of the total input. Western blot analysis of immunoprecipitates was conducted using SNRPA1 Rabbit mAb (A0647) at a dilution of 1:5000. |