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Abbott Laboratories arraytube™
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.
Arraytube™, supplied by Abbott Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/arraytube+system/arraytube+platform/pmc03460768-313-6-7
Average 90 stars, based on 1 article reviews
arraytube™ - by Bioz Stars, 2026-08
90/100 stars

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1) Product Images from "Distinct and overlapping gene regulatory networks in BMP- and HDAC-controlled cell fate determination in the embryonic forebrain"

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

Journal: BMC Genomics

doi: 10.1186/1471-2164-13-298

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.
Figure Legend 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.

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



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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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Image Search Results


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