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anti mhc type 2b  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank anti mhc type 2b
    Anti Mhc Type 2b, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 99/100, based on 843 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti mhc type 2b/product/Developmental Studies Hybridoma Bank
    Average 99 stars, based on 843 article reviews
    anti mhc type 2b - by Bioz Stars, 2026-03
    99/100 stars

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    Developmental Studies Hybridoma Bank mhc iib
    (A) Immunoblot of tibialis anterior (TA) muscles from 6-month-old adult mice after neonatal subcutaneous injection of AAV9.FLEX.A-Fos, a dominant-negative truncation of cFos (A-Fos group), or AAV9.FLEX.GFP control (Con). (B-D) Body weight, body size, and body composition by magnetic resonance imaging (MRI) at 4 months old. (E) Food intake. (F) Illustration of gait parameters, including stride length, stance width, and sway distance. (G–I) Quantification of stride, stance, and sway at 4 months. (J-K) Wire hang test and grip strength at 4 months old. (L-M) Treadmill speed profile and endurance test at 6 months. *p<0.05 by 2-way ANOVA and Bonferroni’s test, n = 7-8 mice. (N) Muscle mass at 6 months old. TA, tibialis anterior; SOL, soleus; EDL, extensor digitorum longus. (O-Q) Immunofluorescence staining of TA muscles from control and A-Fos mice <t>with</t> <t>antibodies</t> or reagents against myosin heavy chain <t>(MHC)</t> isoforms: MHCIIa (green), MHCIIx (black), MHCIIb (red), DAPI (blue), and laminin (white). n = 4–5 mice. (R-S) Glucose tolerance test and the area under the curve (AUC) of the glucose excursion in 3-month-old adult mice. n = 7-8 mice. *p<0.05 by 2-way ANOVA and Bonferroni’s test. Data are mean ± SEM.
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    Developmental Studies Hybridoma Bank myosin heavy chain type 450 iib
    (A) Immunoblot of tibialis anterior (TA) muscles from 6-month-old adult mice after neonatal subcutaneous injection of AAV9.FLEX.A-Fos, a dominant-negative truncation of cFos (A-Fos group), or AAV9.FLEX.GFP control (Con). (B-D) Body weight, body size, and body composition by magnetic resonance imaging (MRI) at 4 months old. (E) Food intake. (F) Illustration of gait parameters, including stride length, stance width, and sway distance. (G–I) Quantification of stride, stance, and sway at 4 months. (J-K) Wire hang test and grip strength at 4 months old. (L-M) Treadmill speed profile and endurance test at 6 months. *p<0.05 by 2-way ANOVA and Bonferroni’s test, n = 7-8 mice. (N) Muscle mass at 6 months old. TA, tibialis anterior; SOL, soleus; EDL, extensor digitorum longus. (O-Q) Immunofluorescence staining of TA muscles from control and A-Fos mice <t>with</t> <t>antibodies</t> or reagents against myosin heavy chain <t>(MHC)</t> isoforms: MHCIIa (green), MHCIIx (black), MHCIIb (red), DAPI (blue), and laminin (white). n = 4–5 mice. (R-S) Glucose tolerance test and the area under the curve (AUC) of the glucose excursion in 3-month-old adult mice. n = 7-8 mice. *p<0.05 by 2-way ANOVA and Bonferroni’s test. Data are mean ± SEM.
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    (A) Immunoblot of tibialis anterior (TA) muscles from 6-month-old adult mice after neonatal subcutaneous injection of AAV9.FLEX.A-Fos, a dominant-negative truncation of cFos (A-Fos group), or AAV9.FLEX.GFP control (Con). (B-D) Body weight, body size, and body composition by magnetic resonance imaging (MRI) at 4 months old. (E) Food intake. (F) Illustration of gait parameters, including stride length, stance width, and sway distance. (G–I) Quantification of stride, stance, and sway at 4 months. (J-K) Wire hang test and grip strength at 4 months old. (L-M) Treadmill speed profile and endurance test at 6 months. *p<0.05 by 2-way ANOVA and Bonferroni’s test, n = 7-8 mice. (N) Muscle mass at 6 months old. TA, tibialis anterior; SOL, soleus; EDL, extensor digitorum longus. (O-Q) Immunofluorescence staining of TA muscles from control and A-Fos mice with antibodies or reagents against myosin heavy chain (MHC) isoforms: MHCIIa (green), MHCIIx (black), MHCIIb (red), DAPI (blue), and laminin (white). n = 4–5 mice. (R-S) Glucose tolerance test and the area under the curve (AUC) of the glucose excursion in 3-month-old adult mice. n = 7-8 mice. *p<0.05 by 2-way ANOVA and Bonferroni’s test. Data are mean ± SEM.

    Journal: bioRxiv

    Article Title: Intermittent AP-1 activation in muscles contributes to exercise-induced health benefits

    doi: 10.64898/2026.01.05.696542

    Figure Lengend Snippet: (A) Immunoblot of tibialis anterior (TA) muscles from 6-month-old adult mice after neonatal subcutaneous injection of AAV9.FLEX.A-Fos, a dominant-negative truncation of cFos (A-Fos group), or AAV9.FLEX.GFP control (Con). (B-D) Body weight, body size, and body composition by magnetic resonance imaging (MRI) at 4 months old. (E) Food intake. (F) Illustration of gait parameters, including stride length, stance width, and sway distance. (G–I) Quantification of stride, stance, and sway at 4 months. (J-K) Wire hang test and grip strength at 4 months old. (L-M) Treadmill speed profile and endurance test at 6 months. *p<0.05 by 2-way ANOVA and Bonferroni’s test, n = 7-8 mice. (N) Muscle mass at 6 months old. TA, tibialis anterior; SOL, soleus; EDL, extensor digitorum longus. (O-Q) Immunofluorescence staining of TA muscles from control and A-Fos mice with antibodies or reagents against myosin heavy chain (MHC) isoforms: MHCIIa (green), MHCIIx (black), MHCIIb (red), DAPI (blue), and laminin (white). n = 4–5 mice. (R-S) Glucose tolerance test and the area under the curve (AUC) of the glucose excursion in 3-month-old adult mice. n = 7-8 mice. *p<0.05 by 2-way ANOVA and Bonferroni’s test. Data are mean ± SEM.

    Article Snippet: Sections were permeabilized with 0.3% Triton X-100 in PBS, blocked with 5% normal goat serum, and incubated overnight with primary antibodies against laminin (Sigma L9393), MHC-IIa (2F7; Developmental Studies Hybridoma Bank), and MHC-IIb (BF-F3; Deutsche Sammlung von Mikroorganismen und Zellkulturen) in blocking buffer.

    Techniques: Western Blot, Muscles, Injection, Dominant Negative Mutation, Control, Magnetic Resonance Imaging, Immunofluorescence, Staining