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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an <t>ArrayTube™</t> (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.
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arraytube platform  (Abbott Laboratories)
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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an <t>ArrayTube™</t> (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.
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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an <t>ArrayTube™</t> (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.
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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an <t>ArrayTube™</t> (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.
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arraytube reader atr03  (Abbott Laboratories)
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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an <t>ArrayTube™</t> (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.
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hybridisation kit appropriate arraytubes  (Abbott Laboratories)
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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an <t>ArrayTube™</t> (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.
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arraytubes  (Abbott Laboratories)
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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an <t>ArrayTube™</t> (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.
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https://www.bioz.com/product/arraytube+system/10__1007_slash_s00216___021___03440___2-100-13-14?v=Abbott+Laboratories
Average 86 stars, based on 1 article reviews
arraytubes - by Bioz Stars, 2026-07
86/100 stars
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Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an ArrayTube™ (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.

Journal: BMC Genomics

Article Title: Distinct and overlapping gene regulatory networks in BMP- and HDAC-controlled cell fate determination in the embryonic forebrain

doi: 10.1186/1471-2164-13-298

Figure Lengend Snippet: Western Blot and ELISA Microarray. Proteins were extracted from TSA (10, 25, 50nM) and BMP2 (10 ng/μl) treated neurosphere cultures 6, 12 or 24 h after treatment. Western Blot for pSmad1/5/8, Smad1/5/8, pStat3, Stat3, pGsk3-beta was performed. Beta-Actin was used as control ( A ). Phosphorylated proteins were quantified using an ArrayTube™ (Alere Technologies, Jena, Germany) based sandwich ELISA microarray. Concentration of pGsk3-beta ( B ) and pErk2 ( C ) in relation to total protein content is presented.

Article Snippet: Phosphorylated proteins were quantified using an ArrayTube™ (Alere Technologies, Jena, Germany) based sandwich ELISA microarray, as previously described [ ].

Techniques: Western Blot, Enzyme-linked Immunosorbent Assay, Microarray, Sandwich ELISA, Concentration Assay