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anti myhc type iib  (Developmental Studies Hybridoma Bank)


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    Structured Review

    Developmental Studies Hybridoma Bank anti myhc type iib
    Anti Myhc Type Iib, 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 myhc type iib/product/Developmental Studies Hybridoma Bank
    Average 99 stars, based on 843 article reviews
    anti myhc type iib - by Bioz Stars, 2026-03
    99/100 stars

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    Developmental Studies Hybridoma Bank myhc iib
    Immunohistochemical representative images of the plantaris muscle for fibre type-specific quantification of displaced myonuclei for 3-day MOV ( A & A ’) and 7-day MOV ( B & B ’). Images show dystrophin (pink), myosin heavy <t>chain</t> <t>IIb</t> <t>(MyHC</t> IIb, red), GFP resident myonuclei (green), and DAPI nuclei (blue). Quantification of displaced myonuclei according to fibre type and condition is reported in C&D with the absolute number of myonuclei per cross-section in panel C and relative number of IIb + or IIb- fibres with one or more displaced myonuclei in panel D . Data are presented as Mean ± SEM and is reported relative to each respective fibre type. (* p ≤ 0.05; ** p ≤ 0.01, *** p ≤ 0.001,**** p ≤ 0.0001; 2-way ANOVA Treatment x Nuclei Label). MOV – mechanical overload, EdU – 5-ethynyl-2’-deoxyuridine, DYS – dystrophin, GFP – green fluorescent protein. Yellow arrows – GFP-, Green arrows – GFP+
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    Developmental Studies Hybridoma Bank myhc type 2b
    Immunohistochemical representative images of the plantaris muscle for fibre type-specific quantification of displaced myonuclei for 3-day MOV ( A & A ’) and 7-day MOV ( B & B ’). Images show dystrophin (pink), myosin heavy <t>chain</t> <t>IIb</t> <t>(MyHC</t> IIb, red), GFP resident myonuclei (green), and DAPI nuclei (blue). Quantification of displaced myonuclei according to fibre type and condition is reported in C&D with the absolute number of myonuclei per cross-section in panel C and relative number of IIb + or IIb- fibres with one or more displaced myonuclei in panel D . Data are presented as Mean ± SEM and is reported relative to each respective fibre type. (* p ≤ 0.05; ** p ≤ 0.01, *** p ≤ 0.001,**** p ≤ 0.0001; 2-way ANOVA Treatment x Nuclei Label). MOV – mechanical overload, EdU – 5-ethynyl-2’-deoxyuridine, DYS – dystrophin, GFP – green fluorescent protein. Yellow arrows – GFP-, Green arrows – GFP+
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    Immunohistochemical representative images of the plantaris muscle for fibre type-specific quantification of displaced myonuclei for 3-day MOV ( A & A ’) and 7-day MOV ( B & B ’). Images show dystrophin (pink), myosin heavy <t>chain</t> <t>IIb</t> <t>(MyHC</t> IIb, red), GFP resident myonuclei (green), and DAPI nuclei (blue). Quantification of displaced myonuclei according to fibre type and condition is reported in C&D with the absolute number of myonuclei per cross-section in panel C and relative number of IIb + or IIb- fibres with one or more displaced myonuclei in panel D . Data are presented as Mean ± SEM and is reported relative to each respective fibre type. (* p ≤ 0.05; ** p ≤ 0.01, *** p ≤ 0.001,**** p ≤ 0.0001; 2-way ANOVA Treatment x Nuclei Label). MOV – mechanical overload, EdU – 5-ethynyl-2’-deoxyuridine, DYS – dystrophin, GFP – green fluorescent protein. Yellow arrows – GFP-, Green arrows – GFP+
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    Developmental Studies Hybridoma Bank myhc type iib
    Loss of C9orf72 induces muscle atrophy and alterations in the muscle fiber composition. Representative optical images of the GCM muscle in C9 +/+ ( A ) and C9 −/− ( B ) mice and myofibers mean cross-sectional area (CSA) distribution ( C ) in both experimental groups. Representative images of coronal sections of the GCM muscle in C9+/+ ( D ) and C9 −/− ( E ) labeled with laminin (white), myosin heavy chain <t>(MyHC)</t> type I <t>(red),</t> <t>IIA</t> (green), IIX (black), and IIB (blue). Analysis of the fiber type composition is shown in ( F ). Type IIX fibers correspond to unlabeled fibers. Representative electron micrographs of C9 +/+ ( G ) and C9 −/− ( H ) GCM muscles, respectively. * = slow (S) motor units. Data are expressed as mean± SEM of six mice per group and examined by two-way ANOVA followed by Fisher’s LSD test. * p < 0.05, ** p < 0.01, *** p < 0.001.
    Myhc Type Iib, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Immunohistochemical representative images of the plantaris muscle for fibre type-specific quantification of displaced myonuclei for 3-day MOV ( A & A ’) and 7-day MOV ( B & B ’). Images show dystrophin (pink), myosin heavy chain IIb (MyHC IIb, red), GFP resident myonuclei (green), and DAPI nuclei (blue). Quantification of displaced myonuclei according to fibre type and condition is reported in C&D with the absolute number of myonuclei per cross-section in panel C and relative number of IIb + or IIb- fibres with one or more displaced myonuclei in panel D . Data are presented as Mean ± SEM and is reported relative to each respective fibre type. (* p ≤ 0.05; ** p ≤ 0.01, *** p ≤ 0.001,**** p ≤ 0.0001; 2-way ANOVA Treatment x Nuclei Label). MOV – mechanical overload, EdU – 5-ethynyl-2’-deoxyuridine, DYS – dystrophin, GFP – green fluorescent protein. Yellow arrows – GFP-, Green arrows – GFP+

    Journal: Skeletal Muscle

    Article Title: Displaced myonuclei are attributable to both resident myonuclear migration and stem cell fusion during mechanical loading in adult skeletal muscle

    doi: 10.1186/s13395-025-00407-0

    Figure Lengend Snippet: Immunohistochemical representative images of the plantaris muscle for fibre type-specific quantification of displaced myonuclei for 3-day MOV ( A & A ’) and 7-day MOV ( B & B ’). Images show dystrophin (pink), myosin heavy chain IIb (MyHC IIb, red), GFP resident myonuclei (green), and DAPI nuclei (blue). Quantification of displaced myonuclei according to fibre type and condition is reported in C&D with the absolute number of myonuclei per cross-section in panel C and relative number of IIb + or IIb- fibres with one or more displaced myonuclei in panel D . Data are presented as Mean ± SEM and is reported relative to each respective fibre type. (* p ≤ 0.05; ** p ≤ 0.01, *** p ≤ 0.001,**** p ≤ 0.0001; 2-way ANOVA Treatment x Nuclei Label). MOV – mechanical overload, EdU – 5-ethynyl-2’-deoxyuridine, DYS – dystrophin, GFP – green fluorescent protein. Yellow arrows – GFP-, Green arrows – GFP+

    Article Snippet: For fibre type assessments, sections were incubated in primaries for MyHC IIb (BF-F3, DSHB) and dystrophin then the appropriate secondary antibodies (isotype-specific for MyHC IIb) before applying DAPI.

    Techniques: Immunohistochemical staining

    Frequency distributions show the occurrences of GFP+ (green) and EdU+ (white) displaced nuclei according to fibre cross sectional area ( A , C , E ). Panels B , D , & F show these frequencies as a proportion of total fibre counts on entire plantaris cross sections. Data are presented as Mean ± SEM and frequency distributions. (* p ≤ 0.05; 2-way ANOVA Treatment x Nuclei Label). MOV – mechanical overload, EdU – 5-ethynyl-2’-deoxyuridine, CSA – cross sectional area, DYS – dystrophin, GFP – green fluorescent protein, MyHC IIb – myosin heavy chain type IIb

    Journal: Skeletal Muscle

    Article Title: Displaced myonuclei are attributable to both resident myonuclear migration and stem cell fusion during mechanical loading in adult skeletal muscle

    doi: 10.1186/s13395-025-00407-0

    Figure Lengend Snippet: Frequency distributions show the occurrences of GFP+ (green) and EdU+ (white) displaced nuclei according to fibre cross sectional area ( A , C , E ). Panels B , D , & F show these frequencies as a proportion of total fibre counts on entire plantaris cross sections. Data are presented as Mean ± SEM and frequency distributions. (* p ≤ 0.05; 2-way ANOVA Treatment x Nuclei Label). MOV – mechanical overload, EdU – 5-ethynyl-2’-deoxyuridine, CSA – cross sectional area, DYS – dystrophin, GFP – green fluorescent protein, MyHC IIb – myosin heavy chain type IIb

    Article Snippet: For fibre type assessments, sections were incubated in primaries for MyHC IIb (BF-F3, DSHB) and dystrophin then the appropriate secondary antibodies (isotype-specific for MyHC IIb) before applying DAPI.

    Techniques:

    Loss of C9orf72 induces muscle atrophy and alterations in the muscle fiber composition. Representative optical images of the GCM muscle in C9 +/+ ( A ) and C9 −/− ( B ) mice and myofibers mean cross-sectional area (CSA) distribution ( C ) in both experimental groups. Representative images of coronal sections of the GCM muscle in C9+/+ ( D ) and C9 −/− ( E ) labeled with laminin (white), myosin heavy chain (MyHC) type I (red), IIA (green), IIX (black), and IIB (blue). Analysis of the fiber type composition is shown in ( F ). Type IIX fibers correspond to unlabeled fibers. Representative electron micrographs of C9 +/+ ( G ) and C9 −/− ( H ) GCM muscles, respectively. * = slow (S) motor units. Data are expressed as mean± SEM of six mice per group and examined by two-way ANOVA followed by Fisher’s LSD test. * p < 0.05, ** p < 0.01, *** p < 0.001.

    Journal: Cells

    Article Title: C9ORF72 Is Pivotal to Maintain a Proper Protein Homeostasis in Mouse Skeletal Muscle

    doi: 10.3390/cells14221765

    Figure Lengend Snippet: Loss of C9orf72 induces muscle atrophy and alterations in the muscle fiber composition. Representative optical images of the GCM muscle in C9 +/+ ( A ) and C9 −/− ( B ) mice and myofibers mean cross-sectional area (CSA) distribution ( C ) in both experimental groups. Representative images of coronal sections of the GCM muscle in C9+/+ ( D ) and C9 −/− ( E ) labeled with laminin (white), myosin heavy chain (MyHC) type I (red), IIA (green), IIX (black), and IIB (blue). Analysis of the fiber type composition is shown in ( F ). Type IIX fibers correspond to unlabeled fibers. Representative electron micrographs of C9 +/+ ( G ) and C9 −/− ( H ) GCM muscles, respectively. * = slow (S) motor units. Data are expressed as mean± SEM of six mice per group and examined by two-way ANOVA followed by Fisher’s LSD test. * p < 0.05, ** p < 0.01, *** p < 0.001.

    Article Snippet: To determine the fiber type, the sections were incubated with MyHC type I (BA-D5, 1:10; DSHB, Iowa City, IA, USA), MyHC type IIa (SC-71, 1:17; DSHB, Iowa City, IA, USA), MyHC type IIb (BF-F3, 1:9; DSHB, Iowa City, IA, USA), Rabbit anti-Laminin (1:100, L9393; Sigma-Aldrich, St. Louis, MO, USA) primary antibodies and respective secondary antibodies, anti-MIgG2b Alexa-flour 564 (A21144, 1:500) (Invitrogen, Waltham, MA, USA), anti-MIgG1 Alexa-flour 488 (A21121, 1:500) (Invitrogen, Waltham, MA, USA), anti-MIgM Alexa-flour 647 (A21046, 1:500; Invitrogen, Waltham, MA, USA), and anti-Rabbit Alexa Fluor 405 (ab175649, 1:500; Abcam, Cambridge, UK).

    Techniques: Labeling, Muscles