mouse anti-aβ 6e10 mab Search Results


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Agilent technologies mouse anti-aβ
Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM <t>Aβ</t> 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations <t>of</t> <t>hyperphosphorylated</t> tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).
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Millipore mouse anti-aβ antibody
Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM <t>Aβ</t> 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations <t>of</t> <t>hyperphosphorylated</t> tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).
Mouse Anti Aβ Antibody, supplied by Millipore, 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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Millipore mouse anti-aβ protein (6e10) antibody
Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM <t>Aβ</t> 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations <t>of</t> <t>hyperphosphorylated</t> tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).
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Covance elisa mouse monoclonal anti-aβ antibodies 6e10
Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM <t>Aβ</t> 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations <t>of</t> <t>hyperphosphorylated</t> tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).
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Senetek plc anti-6e10 (anti-aβ) antibody
Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM <t>Aβ</t> 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations <t>of</t> <t>hyperphosphorylated</t> tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).
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Bio-Rad immunohistochemical ihc staining
Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM <t>Aβ</t> 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations <t>of</t> <t>hyperphosphorylated</t> tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).
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MyBiosource Biotechnology mouse anti-aβ monoclonal antibody 6e10
Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM <t>Aβ</t> 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations <t>of</t> <t>hyperphosphorylated</t> tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).
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Signet Testing n-terminal anti-aβ antibody 6e10 app
(A) Representative samples from the canine parietal cortex show the anti-oligomer A11 antibody detecting the Aβ oligomeric protein at 56kDa. (B) Lower levels and reduced variability of the 56kDa aggregate are seen in the combination treatment group EA despite a large amount of variability within the groups. (CC=control environment/control diet, EC=behavioral enrichment/control diet, CA=control environment/antioxidant diet, EA=behavioral enrichment/antioxidant diet, IP=immunoprecipitated canine sample with anti-Aβ1-16 <t>6E10</t> antibody, numbers on left in A=kilodalton marker, kDa=kilodalton, OD=optical density; GAPDH=glyceraldehyde 3-phosphate dehydrogenase)
N Terminal Anti Aβ Antibody 6e10 App, supplied by Signet Testing, 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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Biosite Inc biotinylated monoclonal mouse-anti-aβ immunoglobulin g1 6e10
(A) Representative samples from the canine parietal cortex show the anti-oligomer A11 antibody detecting the Aβ oligomeric protein at 56kDa. (B) Lower levels and reduced variability of the 56kDa aggregate are seen in the combination treatment group EA despite a large amount of variability within the groups. (CC=control environment/control diet, EC=behavioral enrichment/control diet, CA=control environment/antioxidant diet, EA=behavioral enrichment/antioxidant diet, IP=immunoprecipitated canine sample with anti-Aβ1-16 <t>6E10</t> antibody, numbers on left in A=kilodalton marker, kDa=kilodalton, OD=optical density; GAPDH=glyceraldehyde 3-phosphate dehydrogenase)
Biotinylated Monoclonal Mouse Anti Aβ Immunoglobulin G1 6e10, supplied by Biosite Inc, 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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Jackson Immuno anti aβ antibody 6e10
(A) Representative samples from the canine parietal cortex show the anti-oligomer A11 antibody detecting the Aβ oligomeric protein at 56kDa. (B) Lower levels and reduced variability of the 56kDa aggregate are seen in the combination treatment group EA despite a large amount of variability within the groups. (CC=control environment/control diet, EC=behavioral enrichment/control diet, CA=control environment/antioxidant diet, EA=behavioral enrichment/antioxidant diet, IP=immunoprecipitated canine sample with anti-Aβ1-16 <t>6E10</t> antibody, numbers on left in A=kilodalton marker, kDa=kilodalton, OD=optical density; GAPDH=glyceraldehyde 3-phosphate dehydrogenase)
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Biozol Diagnostica Vertrieb GmbH mouse monoclonal anti-aβ(1–17) (6e10
(A) Representative samples from the canine parietal cortex show the anti-oligomer A11 antibody detecting the Aβ oligomeric protein at 56kDa. (B) Lower levels and reduced variability of the 56kDa aggregate are seen in the combination treatment group EA despite a large amount of variability within the groups. (CC=control environment/control diet, EC=behavioral enrichment/control diet, CA=control environment/antioxidant diet, EA=behavioral enrichment/antioxidant diet, IP=immunoprecipitated canine sample with anti-Aβ1-16 <t>6E10</t> antibody, numbers on left in A=kilodalton marker, kDa=kilodalton, OD=optical density; GAPDH=glyceraldehyde 3-phosphate dehydrogenase)
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OriGene anti-aβ peptide mouse monoclonal antibodies 4g8 and 6e10
(A) Representative samples from the canine parietal cortex show the anti-oligomer A11 antibody detecting the Aβ oligomeric protein at 56kDa. (B) Lower levels and reduced variability of the 56kDa aggregate are seen in the combination treatment group EA despite a large amount of variability within the groups. (CC=control environment/control diet, EC=behavioral enrichment/control diet, CA=control environment/antioxidant diet, EA=behavioral enrichment/antioxidant diet, IP=immunoprecipitated canine sample with anti-Aβ1-16 <t>6E10</t> antibody, numbers on left in A=kilodalton marker, kDa=kilodalton, OD=optical density; GAPDH=glyceraldehyde 3-phosphate dehydrogenase)
Anti Aβ Peptide Mouse Monoclonal Antibodies 4g8 And 6e10, supplied by OriGene, 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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Image Search Results


Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM Aβ 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations of hyperphosphorylated tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).

Journal: PLoS ONE

Article Title: Tg2576 Cortical Neurons That Express Human Ab Are Susceptible to Extracellular Aβ-Induced, K + Efflux Dependent Neurodegeneration

doi: 10.1371/journal.pone.0019026

Figure Lengend Snippet: Tau immunolabelling of the axonal cytoskeleton demonstrated that axonal morphology was similar between wildtype (A) and Tg2576 (B) cortical neurons over 7–14 DIV. Six daily 1 µM Aβ 1-40 treatments of 7DIV wildtype neurons had no discernible effect upon axonal morphology (C). However, substantial changes in tau-labelling were observed in Aβ 1-40 treated Tg2576 neurons (D); including increased intensity of tau immunostaining after 24 hours, followed by blebbing and axonal fragmentation which worsened after four days of treatment (D). Furthermore, after four consecutive days of 1 µM Aβ 1-40 treatment a number of axonal swellings, with dense accumulations of hyperphosphorylated tau, were observed in Tg2576 neuron cultures (E). scale bars = 30 µm (A–D), 15 µm (E).

Article Snippet: For immunocytochemistry, rabbit anti-tau (1∶5000; DAKO), mouse anti-Aβ (6E10; 1∶1000; DAKO) and mouse anti-hyperphosphorylated tau (AT-8; 1∶1000; Chemicon) antibodies were applied, and detected with appropriate Alexa-Fluor-488 or -594 conjugated secondary antibodies at a 1∶1000 concentration (Molecular Probes).

Techniques: Immunostaining

(A) Representative samples from the canine parietal cortex show the anti-oligomer A11 antibody detecting the Aβ oligomeric protein at 56kDa. (B) Lower levels and reduced variability of the 56kDa aggregate are seen in the combination treatment group EA despite a large amount of variability within the groups. (CC=control environment/control diet, EC=behavioral enrichment/control diet, CA=control environment/antioxidant diet, EA=behavioral enrichment/antioxidant diet, IP=immunoprecipitated canine sample with anti-Aβ1-16 6E10 antibody, numbers on left in A=kilodalton marker, kDa=kilodalton, OD=optical density; GAPDH=glyceraldehyde 3-phosphate dehydrogenase)

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Article Title: Synergistic effects of long-term antioxidant diet and behavioral enrichment on beta-amyloid load and non-amyloidogenic processing in aged canines

doi: 10.1523/JNEUROSCI.6194-09.2010

Figure Lengend Snippet: (A) Representative samples from the canine parietal cortex show the anti-oligomer A11 antibody detecting the Aβ oligomeric protein at 56kDa. (B) Lower levels and reduced variability of the 56kDa aggregate are seen in the combination treatment group EA despite a large amount of variability within the groups. (CC=control environment/control diet, EC=behavioral enrichment/control diet, CA=control environment/antioxidant diet, EA=behavioral enrichment/antioxidant diet, IP=immunoprecipitated canine sample with anti-Aβ1-16 6E10 antibody, numbers on left in A=kilodalton marker, kDa=kilodalton, OD=optical density; GAPDH=glyceraldehyde 3-phosphate dehydrogenase)

Article Snippet: The antibodies used in Western blots were β-actin (rabbit, 1:5000, Abcam Inc., Cambridge, MA), GAPDH (rabbit, 1:10,000; Chemicon, Temecula, CA), the N-terminal anti-Aβ antibody 6E10 for APP (mouse, 1:5000, Signet Labs. Inc., Dedham, MA), the C-terminal anti-Aβ antibody CT20 for full length APP and CTF alpha (CTFα) and beta (CTFβ) (rabbit, 1:2000, raised against the C-terminal 20 amino acids of APP), antibodies to clearance enzymes IDE (mouse, 1:250, Covance) and neprilysin (rabbit, 1:50, Abcam Inc., Cambridge, MA), and an antibody to the precursor and mature form of the alpha secretase (αSEC) enzyme TACE/ADAM17 (rabbit, 1:2000, Chemicon, Temecula, CA) or ADAM10 (rabbit, 1:500, Chemicon, Temecula, CA).

Techniques: Immunoprecipitation, Marker