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Novus Biologicals myh2
Muscle fibres and related myosin heavy chains in the upper lip vermilion at different ages. (A) Representative low‐magnification images of MT‐stained sections of the upper lip vermilion at 33 (young) and 66 (old) years old. Bar = 1000 µm; dotted line, analysed regions as the rounded knob‐like tip of OOM; red, muscle fibres; blue, collagenous fibres. (B) High‐magnification images of muscle fibre in the rounded knob‐like tip of the OOM in upper lip vermilion from 27 (young) and 78 (old) years old. Bar = 500 µm; red, muscle fibres; blue, collagenous fibres. (C) Plots of areas occupied by muscle fibres against age. n = 15. * P < 0.05 (Pearson's correlation test). (D) Representative images of immunofluorescence for myosin heavy chain proteins at 27 (young) and 78 (old) years old. Green indicates immunolabelled signal by antibodies specifically targeting MYH1, <t>MYH2,</t> MYH4 and MYH7, respectively. Bar = 20 µm.
Myh2, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Muscle fibres and related myosin heavy chains in the upper lip vermilion at different ages. (A) Representative low‐magnification images of MT‐stained sections of the upper lip vermilion at 33 (young) and 66 (old) years old. Bar = 1000 µm; dotted line, analysed regions as the rounded knob‐like tip of OOM; red, muscle fibres; blue, collagenous fibres. (B) High‐magnification images of muscle fibre in the rounded knob‐like tip of the OOM in upper lip vermilion from 27 (young) and 78 (old) years old. Bar = 500 µm; red, muscle fibres; blue, collagenous fibres. (C) Plots of areas occupied by muscle fibres against age. n = 15. * P < 0.05 (Pearson's correlation test). (D) Representative images of immunofluorescence for myosin heavy chain proteins at 27 (young) and 78 (old) years old. Green indicates immunolabelled signal by antibodies specifically targeting MYH1, MYH2, MYH4 and MYH7, respectively. Bar = 20 µm.

Journal: International Journal of Cosmetic Science

Article Title: Comprehensive histological investigation of age‐related changes in dermal extracellular matrix and muscle fibers in the upper lip vermilion

doi: 10.1111/ics.12622

Figure Lengend Snippet: Muscle fibres and related myosin heavy chains in the upper lip vermilion at different ages. (A) Representative low‐magnification images of MT‐stained sections of the upper lip vermilion at 33 (young) and 66 (old) years old. Bar = 1000 µm; dotted line, analysed regions as the rounded knob‐like tip of OOM; red, muscle fibres; blue, collagenous fibres. (B) High‐magnification images of muscle fibre in the rounded knob‐like tip of the OOM in upper lip vermilion from 27 (young) and 78 (old) years old. Bar = 500 µm; red, muscle fibres; blue, collagenous fibres. (C) Plots of areas occupied by muscle fibres against age. n = 15. * P < 0.05 (Pearson's correlation test). (D) Representative images of immunofluorescence for myosin heavy chain proteins at 27 (young) and 78 (old) years old. Green indicates immunolabelled signal by antibodies specifically targeting MYH1, MYH2, MYH4 and MYH7, respectively. Bar = 20 µm.

Article Snippet: Rat monoclonal antibody to procollagen type I (clone M‐58, ab64409 at 1:100 dilution; Abcam, Cambridge UK), mouse monoclonal antibodies to HAS2 (clone 4E7, NBP2‐37446, 1:400; Novus Biologicals, Littleton, CO), MYH2 (clone TH81, NB100‐65675, 1:500; Novus Biologicals) and MYH4 (clone MF20, 53‐6503‐82, 1:1000; Thermo Fisher Scientific, Waltham, MA), rabbit polyclonal antibodies to procollagen type III (LS‐C664143‐200 1:400; LifeSpan BioSciences, Seattle, WA), HAS1 (HPA067602, 1:200; Atlas Antibodies, Stockholm, Sweden), HAS3 (LS‐B10150‐200, 1:100; LifeSpan BioSciences), cell migration inducing hyaluronidase 1 (CEMIP) (21129‐1‐AP, 1:25; Proteintech, Rosemont, IL), hyaluronidase (HYAL1) (ab85375, 1:100; Abcam), HYAL2 (PA5‐24223, 1:50; Thermo Fisher Scientific), MYH1 (bs‐5885R, 1:500; Bioss Antibodies, Woburn, MA) and MYH7 (22280‐1‐AP, 1:50; Proteintech) were used for primary antibodies.

Techniques: Staining, Immunofluorescence