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Anti hsd17b12

Manufactured by Thermo Fisher Scientific
Sourced in China

Anti-HSD17B12 is a laboratory reagent used for the detection and quantification of the HSD17B12 protein in biological samples. HSD17B12 is an enzyme involved in the biosynthesis of fatty acids and steroids. The Anti-HSD17B12 reagent can be used in various research applications that require the analysis of HSD17B12 expression or activity.

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2 protocols using anti hsd17b12

1

Western Blot Analysis of HSD17B12

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Total proteins were collected from the cell samples after lysis with a lysis buffer (RIPA buffer, Solarbio, Beijing, China) supplemented with protease inhibitors (Solarbio, Beijing, China), phosphatase inhibitors (Solarbio, Beijing, China), and phenylmethylsulfonyl fluoride (Solarbio, Beijing, China). Sodium dodecyl sulfate–polyacrylamide gel electrophoresis was performed on a 10% gel. After filtration through a nitrocellulose membrane (Solarbio), the membrane was sealed with 5% skim milk and treated with primary antibodies (anti-HSD17B12, 1:500, Thermo Fisher Scientific, Shanghai, China; anti-β-actin, 1:3000, Immunoway, Beijing, China) and secondary antibodies. Finally, the membranes were imaged using an Odyssey Clx Imaging System (LICOR, Lincoln, NE, USA) and quantified using Image-Pro Plus software (Media Cybernetics, Rockville, MD, USA).
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2

Western Blot Analysis of HSD17B12

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total proteins were collected from the cell samples after lysis with a lysis buffer (RIPA buffer, Solarbio, Beijing, China) supplemented with protease inhibitors (Solarbio, Beijing, China), phosphatase inhibitors (Solarbio, Beijing, China), and phenylmethylsulfonyl fluoride (Solarbio, Beijing, China). Sodium dodecyl sulfate–polyacrylamide gel electrophoresis was performed on a 10% gel. After filtration through a nitrocellulose membrane (Solarbio), the membrane was sealed with 5% skim milk and treated with primary antibodies (anti-HSD17B12, 1:500, Thermo Fisher Scientific, Shanghai, China; anti-β-actin, 1:3000, Immunoway, Beijing, China) and secondary antibodies. Finally, the membranes were imaged using an Odyssey Clx Imaging System (LICOR, Lincoln, NE, USA) and quantified using Image-Pro Plus software (Media Cybernetics, Rockville, MD, USA).
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