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rabbit polyclonal anti adam 10  (ProSci Incorporated)


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    ProSci Incorporated rabbit polyclonal anti adam 10
    Rabbit Polyclonal Anti Adam 10, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 90/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+adam+10/ADAM10+Antibody/10__1021_slash_jm100308g-111-42-49
    Average 90 stars, based on 22 article reviews
    rabbit polyclonal anti adam 10 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Bioprocessing:

    Article Title: Synthesis and Biological Evaluation of Analogues of a Novel Inhibitor of β-Amyloid Secretion
    Article Snippet: Enakshi Chakrabarti, Subrata Ghosh, Sushabhan Sadhukhan, Lawrence Sayre, ) Gregory P. Tochtrop,* and Jonathan D. Smith* Department of Cell Biology, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, Ohio 44195, and Department of Chemistry, Case Western Reserve University, 2074 Adlebert Road, Cleveland, Ohio 44106.. Current address: Department of Basic Sciences and Social Sciences, North-Eastern Hill University, Mawlai Umshing, Shillong-793 022, India. ). Deceased.



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    Expression analysis showing the normalized mRNA levels of ( A ) AT 1 R, ( B ) APP, ( C ) ADAM 10, BACE1 and PS1. n = 7 for AT1R and n = 6 for all others. CTs (threshold cycles) were used as the readout. The results were obtained using the comparative Ct method and the arithmetic formula 2 −ΔΔCt . Data were normalized to β-actin and represented as fold increases over saline controls. * p <0.05 or ** p <0.01 versus the control group receiving saline infusion.
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    Expression analysis showing the normalized mRNA levels of ( A ) AT 1 R, ( B ) APP, ( C ) ADAM 10, BACE1 and PS1. n = 7 for AT1R and n = 6 for all others. CTs (threshold cycles) were used as the readout. The results were obtained using the comparative Ct method and the arithmetic formula 2 −ΔΔCt . Data were normalized to β-actin and represented as fold increases over saline controls. * p <0.05 or ** p <0.01 versus the control group receiving saline infusion.
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    Image Search Results


    Expression analysis showing the normalized mRNA levels of ( A ) AT 1 R, ( B ) APP, ( C ) ADAM 10, BACE1 and PS1. n = 7 for AT1R and n = 6 for all others. CTs (threshold cycles) were used as the readout. The results were obtained using the comparative Ct method and the arithmetic formula 2 −ΔΔCt . Data were normalized to β-actin and represented as fold increases over saline controls. * p <0.05 or ** p <0.01 versus the control group receiving saline infusion.

    Journal: PLoS ONE

    Article Title: Central Angiotensin II Stimulation Promotes β Amyloid Production in Sprague Dawley Rats

    doi: 10.1371/journal.pone.0016037

    Figure Lengend Snippet: Expression analysis showing the normalized mRNA levels of ( A ) AT 1 R, ( B ) APP, ( C ) ADAM 10, BACE1 and PS1. n = 7 for AT1R and n = 6 for all others. CTs (threshold cycles) were used as the readout. The results were obtained using the comparative Ct method and the arithmetic formula 2 −ΔΔCt . Data were normalized to β-actin and represented as fold increases over saline controls. * p <0.05 or ** p <0.01 versus the control group receiving saline infusion.

    Article Snippet: The following primary antibodies and working dilutions were used: rabbit polyclonal anti-APP carboxyl terminal (Sigma, 1∶5,000), rabbit polyclonal anti-ADAM 10 (Millipore, 1∶500), rabbit monoclonal anti-BACE1 (Cell Signaling, 1∶500), mouse monoclonal anti-PS1 that recognizes the PS1 amino terminal (Abcam, 1∶250), mouse monoclonal anti-AT 1 R, which recognizes the AT 1 R carboxyl terminal (Abcam, 1∶125), and mouse monoclonal anti-β actin (Sigma, 1∶1,000).

    Techniques: Expressing

    The same gels were blotted for β-actin as an internal standard. n = 6 for each group. ( A ) Representative enhanced chemiluminescence radiographs of immunoblots showing the immunoactivities of AT 1 R, APP, ADAM 10, BACE1, PS1, C83, C99 and β-actin. Density analysis showing levels of ( B ) AT 1 R, ( C ) APP, ( D ) ADAM 10, BACE1, and PS1, ( E ) ( F ) C83 and C99. Data in ( B–E ) were normalized by dividing the density of the AT 1 R, ADAM 10, BACE1, PS1, C83 and C99 bands by the density of the β-actin band. Data in ( F ) were normalized by dividing the density of the C83 and C99 band by that of the β-actin band and then the imAPP band. All data were represented as fold increases over the saline controls. * p <0.05 or ** p <0.01 versus the control group receiving saline infusion. imAPP, immature APP; mAPP, mature APP; imADAM 10, immature ADAM 10;mADAM 10, mature ADAM 10.

    Journal: PLoS ONE

    Article Title: Central Angiotensin II Stimulation Promotes β Amyloid Production in Sprague Dawley Rats

    doi: 10.1371/journal.pone.0016037

    Figure Lengend Snippet: The same gels were blotted for β-actin as an internal standard. n = 6 for each group. ( A ) Representative enhanced chemiluminescence radiographs of immunoblots showing the immunoactivities of AT 1 R, APP, ADAM 10, BACE1, PS1, C83, C99 and β-actin. Density analysis showing levels of ( B ) AT 1 R, ( C ) APP, ( D ) ADAM 10, BACE1, and PS1, ( E ) ( F ) C83 and C99. Data in ( B–E ) were normalized by dividing the density of the AT 1 R, ADAM 10, BACE1, PS1, C83 and C99 bands by the density of the β-actin band. Data in ( F ) were normalized by dividing the density of the C83 and C99 band by that of the β-actin band and then the imAPP band. All data were represented as fold increases over the saline controls. * p <0.05 or ** p <0.01 versus the control group receiving saline infusion. imAPP, immature APP; mAPP, mature APP; imADAM 10, immature ADAM 10;mADAM 10, mature ADAM 10.

    Article Snippet: The following primary antibodies and working dilutions were used: rabbit polyclonal anti-APP carboxyl terminal (Sigma, 1∶5,000), rabbit polyclonal anti-ADAM 10 (Millipore, 1∶500), rabbit monoclonal anti-BACE1 (Cell Signaling, 1∶500), mouse monoclonal anti-PS1 that recognizes the PS1 amino terminal (Abcam, 1∶250), mouse monoclonal anti-AT 1 R, which recognizes the AT 1 R carboxyl terminal (Abcam, 1∶125), and mouse monoclonal anti-β actin (Sigma, 1∶1,000).

    Techniques: Western Blot