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rabbit  (Alomone Labs)


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    Structured Review

    Alomone Labs rabbit
    Rabbit, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 90/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc+003+ag/pm37801990-45-9-13?v=Alomone+Labs
    Average 90 stars, based on 2 article reviews
    rabbit - by Bioz Stars, 2026-07
    90/100 stars

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    Image Search Results


    A . Detection of ~240 kDa bands corresponding to Ca V 1.2 in ventricular tissue from sham and OVX mice. Na/K ATPase (110 kDa band) was used as a loading control (15 µg of protein were loaded in each lane). Average Ca V 1.2 band intensity was lower in OVX ventricular tissue compared to sham controls (n=3 hearts/group). B . Representative immunoblot illustrating ~116 kDa bands corresponding to NCX in sham and OVX ventricle. The loading control was Na-K ATPase as in A. Mean normalized NCX band intensity was similar in ventricular tissue from sham and OVX mice (n=3 hearts in each group). C . Detection of ~110 kDa bands corresponding to SERCA2 in the ventricles of sham and OVX mice. Amido black was used as a loading control (60 µg of protein were loaded in each lane). Average intensity of the SERCA2 bands was similar in sham and OVX ventricles (n=3 hearts in each group). In experiments where Na-K ATPase was used as a loading control, there was no significant difference in Na-K ATPase protein levels between sham and OVX (t-test, p=0.164) (*denotes p<0.05; t-test)..

    Journal: PLoS ONE

    Article Title: The Impact of Ovariectomy on Calcium Homeostasis and Myofilament Calcium Sensitivity in the Aging Mouse Heart

    doi: 10.1371/journal.pone.0074719

    Figure Lengend Snippet: A . Detection of ~240 kDa bands corresponding to Ca V 1.2 in ventricular tissue from sham and OVX mice. Na/K ATPase (110 kDa band) was used as a loading control (15 µg of protein were loaded in each lane). Average Ca V 1.2 band intensity was lower in OVX ventricular tissue compared to sham controls (n=3 hearts/group). B . Representative immunoblot illustrating ~116 kDa bands corresponding to NCX in sham and OVX ventricle. The loading control was Na-K ATPase as in A. Mean normalized NCX band intensity was similar in ventricular tissue from sham and OVX mice (n=3 hearts in each group). C . Detection of ~110 kDa bands corresponding to SERCA2 in the ventricles of sham and OVX mice. Amido black was used as a loading control (60 µg of protein were loaded in each lane). Average intensity of the SERCA2 bands was similar in sham and OVX ventricles (n=3 hearts in each group). In experiments where Na-K ATPase was used as a loading control, there was no significant difference in Na-K ATPase protein levels between sham and OVX (t-test, p=0.164) (*denotes p<0.05; t-test)..

    Article Snippet: Antibodies used were rabbit anti- Ca v 1.2 polyclonal antibody (Alomone, ACC-003-AG; 1:2000), mouse anti-NCX monoclonal antibody (SWANT, R3F1; 1:1000), mouse anti-SERCA2 monoclonal antibody (Affinity Bioreagents, MA3-919; 1:2000) and rabbit anti-Na/KATPase polyclonal antibody (Abcam; 1:2000).

    Techniques: Western Blot

    Journal: PLoS ONE

    Article Title: The Impact of Ovariectomy on Calcium Homeostasis and Myofilament Calcium Sensitivity in the Aging Mouse Heart

    doi: 10.1371/journal.pone.0074719

    Figure Lengend Snippet: Comparison of Key Ca 2+ Handling Mechanisms in Hearts and Cardiomyocytes From Young Adult OVX and Aged OVX Female Mice.

    Article Snippet: Antibodies used were rabbit anti- Ca v 1.2 polyclonal antibody (Alomone, ACC-003-AG; 1:2000), mouse anti-NCX monoclonal antibody (SWANT, R3F1; 1:1000), mouse anti-SERCA2 monoclonal antibody (Affinity Bioreagents, MA3-919; 1:2000) and rabbit anti-Na/KATPase polyclonal antibody (Abcam; 1:2000).

    Techniques: In Vivo, Activity Assay, Expressing

    Representative blots are shown for VDCC (A). The amount of the alpha-1c subunit of VDCC was determined as the ratio of VDCC to β-actin (B). Results are expressed as the mean ± SEM (n = 6). ** P <0.01 vs each 8-week rat strain. Confocal measurement of VDCC (C) was performed in rat aortic segments (14 µm).

    Journal: PLoS ONE

    Article Title: Attenuation of L-Type Ca 2+ Channel Expression and Vasomotor Response in the Aorta with Age in Both Wistar-Kyoto and Spontaneously Hypertensive Rats

    doi: 10.1371/journal.pone.0088975

    Figure Lengend Snippet: Representative blots are shown for VDCC (A). The amount of the alpha-1c subunit of VDCC was determined as the ratio of VDCC to β-actin (B). Results are expressed as the mean ± SEM (n = 6). ** P <0.01 vs each 8-week rat strain. Confocal measurement of VDCC (C) was performed in rat aortic segments (14 µm).

    Article Snippet: Rabbit anti-Cav1.2, the alpha-1c subunit VDCC, primary antibody was obtained from Alomone Labs (Jerusalem, Israel).

    Techniques: