heart tissue Search Results


heart brain lysate cross reactivity varying amounts  (Novus Biologicals)
90
Novus Biologicals heart brain lysate cross reactivity varying amounts
Heart Brain Lysate Cross Reactivity Varying Amounts, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Heart+Membrane+Tissue+Lysate+(Adult+Membrane+Normal)/pm39450141-232-4-17
Average 90 stars, based on 1 article reviews
heart brain lysate cross reactivity varying amounts - by Bioz Stars, 2026-08
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mouse heart tissues  (Cell Signaling Technology Inc)
93
Cell Signaling Technology Inc mouse heart tissues
Mouse Heart Tissues, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Mouse+Heart+Tissue+Control+Extracts/pm30053027-184-0-9
Average 93 stars, based on 1 article reviews
mouse heart tissues - by Bioz Stars, 2026-08
93/100 stars
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human heart whole tissue lysate  (Novus Biologicals)
92
Novus Biologicals human heart whole tissue lysate
Human Heart Whole Tissue Lysate, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Heart+Whole+Tissue+Lysate+(Adult+Whole+Normal)/pmc05531073-109-0-16
Average 92 stars, based on 1 article reviews
human heart whole tissue lysate - by Bioz Stars, 2026-08
92/100 stars
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human heart aorta valve whole tissue lysate  (Novus Biologicals)
90
Novus Biologicals human heart aorta valve whole tissue lysate
Human Heart Aorta Valve Whole Tissue Lysate, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Heart+Aorta+Valve+Whole+Tissue+Lysate+(Adult+Whole+Normal)/pmc04766568-177-25-34
Average 90 stars, based on 1 article reviews
human heart aorta valve whole tissue lysate - by Bioz Stars, 2026-08
90/100 stars
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human heart tissue cryosections  (OriGene)
92
OriGene human heart tissue cryosections
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Human Heart Tissue Cryosections, supplied by OriGene, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Frozen+Tissue+Sections%2C+Heart/pm38771868-337-0-7
Average 92 stars, based on 1 article reviews
human heart tissue cryosections - by Bioz Stars, 2026-08
92/100 stars
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cytochrome c  (R&D Systems)
94
R&D Systems cytochrome c
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Cytochrome C, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Cytochrome+c+(Human+Heart+Tissue)+Protein%2C+CF/pm33308446-294-15-23
Average 94 stars, based on 1 article reviews
cytochrome c - by Bioz Stars, 2026-08
94/100 stars
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human tissue protein extracts  (Novus Biologicals)
91
Novus Biologicals human tissue protein extracts
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Human Tissue Protein Extracts, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Cytochrome+c+(Human+Heart+Tissue)+Protein%2C+CF/pmc06879868-197-3-10
Average 91 stars, based on 1 article reviews
human tissue protein extracts - by Bioz Stars, 2026-08
91/100 stars
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human heart tissues  (Novus Biologicals)
92
Novus Biologicals human heart tissues
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Human Heart Tissues, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Heart+Whole+Tissue+Lysate+(Adult+Whole+Normal)/pm34744144-33-10-19
Average 92 stars, based on 1 article reviews
human heart tissues - by Bioz Stars, 2026-08
92/100 stars
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heart aorta valve  (Novus Biologicals)
93
Novus Biologicals heart aorta valve
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Heart Aorta Valve, 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
https://www.bioz.com/product/heart+tissue/Human+Heart+Aorta+Valve+Whole+Tissue+Lysate+(Adult+Whole+Normal)/pmc12354682-316-6-9
Average 93 stars, based on 1 article reviews
heart aorta valve - by Bioz Stars, 2026-08
93/100 stars
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heart tissue lysate  (Novus Biologicals)
91
Novus Biologicals heart tissue lysate
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Heart Tissue Lysate, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Heart+Membrane+Tissue+Lysate+(Adult+Membrane+Normal)/bio_rxiv__2021__12__07__471543-175-12-15
Average 91 stars, based on 1 article reviews
heart tissue lysate - by Bioz Stars, 2026-08
91/100 stars
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adult human heart tissue lysate  (Novus Biologicals)
92
Novus Biologicals adult human heart tissue lysate
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Adult Human Heart Tissue Lysate, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Human+Heart+Whole+Tissue+Lysate+(Adult+Whole+Normal)/pmc11501091-355-4-9
Average 92 stars, based on 1 article reviews
adult human heart tissue lysate - by Bioz Stars, 2026-08
92/100 stars
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human total rnas  (OriGene)
90
OriGene human total rnas
Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of <t>cryosections</t> of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.
Human Total Rnas, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/heart+tissue/Tissue+Total+RNA%2C+Heart/10__1042_slash_bsr20170975-70-0-6
Average 90 stars, based on 1 article reviews
human total rnas - by Bioz Stars, 2026-08
90/100 stars
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Image Search Results


Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of cryosections of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Article Title: Matriglycan maintains t-tubule structural integrity in cardiac muscle.

doi: 10.1073/pnas.2402890121

Figure Lengend Snippet: Fig. 4. The t-tubule network develops in the absence of O-mannosylated α-DG. (A and B) Immunofluorescence of cryosections of ventricles from control and Pomt1 cKO mice to detect matriglycan (A and B) and β-DG (B). Ten µm cryosections were used in A. (Scale bar, 10 µm.) Sixteen µm cryosections were used in B. (Scale bar, 5 µm.) (C) FM 464-FX fluorescence of whole left ventricles to detect plasma membranes, including t-tubule membranes. (Scale bar, 20 µm.) (D) Quantification of the percent of myofibers with normal or disrupted t-tubule staining within a 90× magnification field. (E) Line scan analysis to determine the peak signal intensity of FM 464-FX labeled t-tubules (TT). (F) Number of t-tubules observed within 16 µm regions. Image analysis was performed on hearts of mice from both sexes (n = 4 controls; n = 5 cKO). Unpaired t tests with the Holm–Sidak post hoc test were performed. Data are expressed as mean ± SD.

Article Snippet: Human heart tissue cryosections were purchased from OriGene (CS616190; CS616185; Rockville, Maryland, USA).

Techniques: Immunofluorescence, Control, Fluorescence, Clinical Proteomics, Staining, Labeling