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Micromass UK Limited
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Brinkmann Instruments
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Citta Pharmaceuticals
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Human Protein Atlas
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Brinkmann Instruments
molecular cloning and expression of human udp-dxylose:proteoglycan core protein b-d-xylosyltransferase and its first isoform xt-ii ![]() Molecular Cloning And Expression Of Human Udp Dxylose:Proteoglycan Core Protein B D Xylosyltransferase And Its First Isoform Xt Ii, supplied by Brinkmann Instruments, 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/result/molecular cloning and expression of human udp-dxylose:proteoglycan core protein b-d-xylosyltransferase and its first isoform xt-ii/product/Brinkmann Instruments Average 90 stars, based on 1 article reviews
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Janssen
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TDP2 HEK293T cell transient overexpression lysate as WB positive control
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Image Search Results
Journal: Bone Marrow Research
Article Title: A Simplified Method for the Aspiration of Bone Marrow from Patients Undergoing Hip and Knee Joint Replacement for Isolating Mesenchymal Stem Cells and In Vitro Chondrogenesis
doi: 10.1155/2016/3152065
Figure Lengend Snippet: List of antibodies used for IHC of micromass cartilages.
Article Snippet: Tuan laboratory showed that COL2A1 gene was expressed at day 14 and increased at days 21 and 28, the similar pattern of
Techniques: Plasmid Preparation
Journal: Bone Marrow Research
Article Title: A Simplified Method for the Aspiration of Bone Marrow from Patients Undergoing Hip and Knee Joint Replacement for Isolating Mesenchymal Stem Cells and In Vitro Chondrogenesis
doi: 10.1155/2016/3152065
Figure Lengend Snippet: IHC of COL II (a) and COL I (b) in micromass cartilages. COL II expressed at weeks 2–4 (a), and COL I expressed at weeks 1–4 (week 3 not shown, b), in micromass cartilages. Articular cartilage of rat knee and human tracheal cartilage served as positive control for COL II; higher magnification of week 4 micromass cartilage shows that it is present in ECM (a). COL I is absent in native articular cartilage in positive control and is present in bone only, whereas COL I is expressed at low level in the bioengineered micromass cartilage (b). Micromass cartilage and rat tibia showed no staining when primary antibody was missing and only mouse IgG was present, which served as negative control (c). M, meniscus; AC, articular cartilage; B, bone; mm, micromass.
Article Snippet: Tuan laboratory showed that COL2A1 gene was expressed at day 14 and increased at days 21 and 28, the similar pattern of
Techniques: Positive Control, Staining, Negative Control
Journal: Bone Marrow Research
Article Title: A Simplified Method for the Aspiration of Bone Marrow from Patients Undergoing Hip and Knee Joint Replacement for Isolating Mesenchymal Stem Cells and In Vitro Chondrogenesis
doi: 10.1155/2016/3152065
Figure Lengend Snippet: IHC of COL X shows the presence of weak signal in week 3 and week 4 micromass cartilage (a), whereas apoptosis assays show no apoptosis in micromass cartilage (b). Mouse decalcified P1 limb showed hypertrophic chondrocytes zone (arrows) as positive control for COL X (a). Mouse involuting MG (mammary gland) at postpartum day 4 showed apoptotic cells in mammary epithelium (arrow) that served as positive control, whereas no apoptotic cell was found at week 4 in micromass cartilage compared with positive control. mm, micromass.
Article Snippet: Tuan laboratory showed that COL2A1 gene was expressed at day 14 and increased at days 21 and 28, the similar pattern of
Techniques: Positive Control
Journal: Bone Marrow Research
Article Title: A Simplified Method for the Aspiration of Bone Marrow from Patients Undergoing Hip and Knee Joint Replacement for Isolating Mesenchymal Stem Cells and In Vitro Chondrogenesis
doi: 10.1155/2016/3152065
Figure Lengend Snippet: IHC showed that micromass cartilage expressed aggrecan and COL VI at all the time points (weeks 1–4, a, b). Articular cartilage of rat knee expressed aggrecan and served as positive control (a). Human tracheal cartilage served as positive control for COL VI and showed that COL VI is pericellular in location in native cartilage (b). Higher magnification of week 4 bioengineered micromass cartilage also shows the pericellular localization of COL VI (arrowheads, b). Rat knee (a) and micromass cartilage (b) were used as negative control with rabbit IgG polyclonal and without primary antibody. M, meniscus; AC, articular cartilage; B, bone; mm, micromass.
Article Snippet: Tuan laboratory showed that COL2A1 gene was expressed at day 14 and increased at days 21 and 28, the similar pattern of
Techniques: Positive Control, Negative Control