anti adam17 antibody Search Results


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Bioss adam17 polyclonal antibody
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Biozol Diagnostica Vertrieb GmbH polyclonal rabbit anti-human adam17 antibody
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Biogenix Inc anti-adam17 antibody
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AnaSpec anti-adam-17 rabbit polyclonal antibody ct
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MedImmune llc anti adam17 antibody
Properties of mAbs developed against metzincin targets
Anti Adam17 Antibody, supplied by MedImmune llc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Triple Point Biologics adam17 antibody
Properties of mAbs developed against metzincin targets
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Triple Point Biologics anti adam17 antibody
ADAM10 and <t>ADAM17</t> expression in thrombopoietic cells. (A) CD34+ haematopoietic progenitor cells were cultured for 12 d in the presence of thrombopoietin to induce megakaryocyte differentiation. On days 0, 6, 9, and 12 mRNA expression of ADAM10 and ADAM17 was analyzed by qPCR. Representative data of one from a total of 3 biologic experiments performed in technical replicates are shown. (B) Platelets from healthy donors were either left untreated (resting) or activated with ADP, collagen or thrombin until aggregation was visible (for a maximum of 30 s to prevent clumping) as described previously.23 Then FACS analysis of ADAM10 or ADAM17 expression was performed. (C) Platelets were either left untreated (resting) or activated by exposure to the platelet superagonist TRAP-6 (5 µM) for 5 minutes. Then ADAM10 and ADAM17 levels in platelet pellets and releasate was analyzed by Western blot. In (B-C), representative data of one experiment from a total of at least 4 with similar results are shown. (D) Resting platelets from healthy donors and patients with NSCLC were analyzed by FACS as described in (B). Statistically significant differences (p<0.05, Kolmogorov-Smirnov test) are indicated by *.
Anti Adam17 Antibody, supplied by Triple Point Biologics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Properties of mAbs developed against metzincin targets

Journal: British Journal of Pharmacology

Article Title: Monoclonal antibodies against metzincin targets

doi: 10.1111/bph.14186

Figure Lengend Snippet: Properties of mAbs developed against metzincin targets

Article Snippet: Another anti‐ADAM17 antibody was developed by MedImmune, LLC.

Techniques: Concentration Assay, In Vitro, Ex Vivo, In Vivo, Activity Assay, Inhibition, Activation Assay, Lysis

ADAM10 and ADAM17 expression in thrombopoietic cells. (A) CD34+ haematopoietic progenitor cells were cultured for 12 d in the presence of thrombopoietin to induce megakaryocyte differentiation. On days 0, 6, 9, and 12 mRNA expression of ADAM10 and ADAM17 was analyzed by qPCR. Representative data of one from a total of 3 biologic experiments performed in technical replicates are shown. (B) Platelets from healthy donors were either left untreated (resting) or activated with ADP, collagen or thrombin until aggregation was visible (for a maximum of 30 s to prevent clumping) as described previously.23 Then FACS analysis of ADAM10 or ADAM17 expression was performed. (C) Platelets were either left untreated (resting) or activated by exposure to the platelet superagonist TRAP-6 (5 µM) for 5 minutes. Then ADAM10 and ADAM17 levels in platelet pellets and releasate was analyzed by Western blot. In (B-C), representative data of one experiment from a total of at least 4 with similar results are shown. (D) Resting platelets from healthy donors and patients with NSCLC were analyzed by FACS as described in (B). Statistically significant differences (p<0.05, Kolmogorov-Smirnov test) are indicated by *.

Journal: Oncoimmunology

Article Title: Platelet-mediated shedding of NKG2D ligands impairs NK cell immune-surveillance of tumor cells

doi: 10.1080/2162402X.2017.1364827

Figure Lengend Snippet: ADAM10 and ADAM17 expression in thrombopoietic cells. (A) CD34+ haematopoietic progenitor cells were cultured for 12 d in the presence of thrombopoietin to induce megakaryocyte differentiation. On days 0, 6, 9, and 12 mRNA expression of ADAM10 and ADAM17 was analyzed by qPCR. Representative data of one from a total of 3 biologic experiments performed in technical replicates are shown. (B) Platelets from healthy donors were either left untreated (resting) or activated with ADP, collagen or thrombin until aggregation was visible (for a maximum of 30 s to prevent clumping) as described previously.23 Then FACS analysis of ADAM10 or ADAM17 expression was performed. (C) Platelets were either left untreated (resting) or activated by exposure to the platelet superagonist TRAP-6 (5 µM) for 5 minutes. Then ADAM10 and ADAM17 levels in platelet pellets and releasate was analyzed by Western blot. In (B-C), representative data of one experiment from a total of at least 4 with similar results are shown. (D) Resting platelets from healthy donors and patients with NSCLC were analyzed by FACS as described in (B). Statistically significant differences (p<0.05, Kolmogorov-Smirnov test) are indicated by *.

Article Snippet: Membrane was blocked for 1 h at room temperature with Roti-Block, followed by overnight incubation at 4°C with anti-ADAM10 or anti-ADAM17 antibody (1:1000 each; Cell Signaling Technologies and Triple Point Biologics, respectively).

Techniques: Expressing, Cell Culture, Western Blot