primary human skeletal muscle cells myoblasts Search Results


sk 1111  (Cook MyoSite Inc)
94
Cook MyoSite Inc sk 1111
Sk 1111, supplied by Cook MyoSite Inc, 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/result/sk 1111/product/Cook MyoSite Inc
Average 94 stars, based on 1 article reviews
sk 1111 - by Bioz Stars, 2026-06
94/100 stars
  Buy from Supplier
human skeletal muscle primary myoblasts cat# skb-f  (ZenBio)
90
ZenBio human skeletal muscle primary myoblasts cat# skb-f
Human Skeletal Muscle Primary Myoblasts Cat# Skb F, supplied by ZenBio, 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/result/human skeletal muscle primary myoblasts cat# skb-f/product/ZenBio
Average 90 stars, based on 1 article reviews
human skeletal muscle primary myoblasts cat# skb-f - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
primary human skeletal muscle myoblasts skms  (Lonza)
90
Lonza primary human skeletal muscle myoblasts skms
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Primary Human Skeletal Muscle Myoblasts Skms, supplied by Lonza, 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/result/primary human skeletal muscle myoblasts skms/product/Lonza
Average 90 stars, based on 1 article reviews
primary human skeletal muscle myoblasts skms - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
human skeletal muscle myoblasts primary cell strains  (Lonza)
90
Lonza human skeletal muscle myoblasts primary cell strains
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Human Skeletal Muscle Myoblasts Primary Cell Strains, supplied by Lonza, 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/result/human skeletal muscle myoblasts primary cell strains/product/Lonza
Average 90 stars, based on 1 article reviews
human skeletal muscle myoblasts primary cell strains - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
human skeletal muscle myoblast, or satellite cells  (Lonza)
90
Lonza human skeletal muscle myoblast, or satellite cells
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Human Skeletal Muscle Myoblast, Or Satellite Cells, supplied by Lonza, 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/result/human skeletal muscle myoblast, or satellite cells/product/Lonza
Average 90 stars, based on 1 article reviews
human skeletal muscle myoblast, or satellite cells - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
human myoblasts primary cell culture normal human skeletal muscle cells from a single donor  (Lonza)
90
Lonza human myoblasts primary cell culture normal human skeletal muscle cells from a single donor
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Human Myoblasts Primary Cell Culture Normal Human Skeletal Muscle Cells From A Single Donor, supplied by Lonza, 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/result/human myoblasts primary cell culture normal human skeletal muscle cells from a single donor/product/Lonza
Average 90 stars, based on 1 article reviews
human myoblasts primary cell culture normal human skeletal muscle cells from a single donor - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
differentiated muscle cells from isolated human skeletal myoblasts  (Lonza)
90
Lonza differentiated muscle cells from isolated human skeletal myoblasts
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Differentiated Muscle Cells From Isolated Human Skeletal Myoblasts, supplied by Lonza, 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/result/differentiated muscle cells from isolated human skeletal myoblasts/product/Lonza
Average 90 stars, based on 1 article reviews
differentiated muscle cells from isolated human skeletal myoblasts - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
human primary skeletal muscle myoblasts skgmtm-2  (Lonza)
90
Lonza human primary skeletal muscle myoblasts skgmtm-2
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Human Primary Skeletal Muscle Myoblasts Skgmtm 2, supplied by Lonza, 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/result/human primary skeletal muscle myoblasts skgmtm-2/product/Lonza
Average 90 stars, based on 1 article reviews
human primary skeletal muscle myoblasts skgmtm-2 - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
rna extracted from normal human skeletal muscle myoblast cells  (Lonza)
90
Lonza rna extracted from normal human skeletal muscle myoblast cells
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Rna Extracted From Normal Human Skeletal Muscle Myoblast Cells, supplied by Lonza, 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/result/rna extracted from normal human skeletal muscle myoblast cells/product/Lonza
Average 90 stars, based on 1 article reviews
rna extracted from normal human skeletal muscle myoblast cells - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
endogenous adenosine receptor expressed primary human skeletal muscle myoblasts  (Lonza)
90
Lonza endogenous adenosine receptor expressed primary human skeletal muscle myoblasts
Mitochondrial abundance and activity in human <t>primary</t> <t>myoblasts</t> were differentially affected by FFAs. <t>SkMs</t> were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).
Endogenous Adenosine Receptor Expressed Primary Human Skeletal Muscle Myoblasts, supplied by Lonza, 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/result/endogenous adenosine receptor expressed primary human skeletal muscle myoblasts/product/Lonza
Average 90 stars, based on 1 article reviews
endogenous adenosine receptor expressed primary human skeletal muscle myoblasts - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
human skeletal muscle myoblast primary cell culture serum free differentiation media  (Celprogen Inc)
N/A
Human Skeletal Muscle Primary Cell Culture Serum Free Differentiation Media. This product is also available with Serum Cat# M36018-18DS This product would require pre-coated flasks with Human Skeletal Muscle Primary Cell Culture Extra-cellular Differentiation Matrix
   Buy from Supplier
human skeletal muscle myoblast primary cell culture differentiation media with serum  (Celprogen Inc)
N/A
Human Skeletal Muscle Myoblast Primary Cell Culture Differentiation Media with Serum This product is also available without Serum Cat# M36018-18D This product would require pre-coated flasks with Human Skeletal Muscle Myoblast Primary Cell Culture Extra-cellular
   Buy from Supplier

Image Search Results


Mitochondrial abundance and activity in human primary myoblasts were differentially affected by FFAs. SkMs were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).

Journal: Biology

Article Title: Free Fatty Acid Species Differentially Modulate the Inflammatory Gene Response in Primary Human Skeletal Myoblasts

doi: 10.3390/biology10121318

Figure Lengend Snippet: Mitochondrial abundance and activity in human primary myoblasts were differentially affected by FFAs. SkMs were treated with FAs conjugated with BSA or BSA alone (control). After 48 h, SkMs were incubated with MitoTracker Red ( a ) or Orange ( b ). Fluorescence images at identical settings and exposure times from 3 sets of experiments were simultaneously imported into the analysis software, processed to 8-bit images and analyzed. The integrated fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of the relative fluorescence intensity of MitoTracker Red (white bars) or Orange (black bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*), p ≤ 0.01 (**).

Article Snippet: Primary human skeletal muscle myoblasts (SkMs) were obtained from Lonza, Basel, Switzerland (CC-2561).

Techniques: Activity Assay, Control, Incubation, Fluorescence, Software, Comparison

FFAs do not affect the desmin expression pattern in human primary myoblasts. ( a ) SkMs were treated with FAs conjugated with BSA or BSA alone (control) before DAPI and desmin staining. ( b ) Fluorescence images from 3 sets of experiments were analyzed, as described in the legend to . The number of DAPI-positive FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The data are presented as the mean ± SD of cell number (dotted bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*). p ≤ 0.01 (**).

Journal: Biology

Article Title: Free Fatty Acid Species Differentially Modulate the Inflammatory Gene Response in Primary Human Skeletal Myoblasts

doi: 10.3390/biology10121318

Figure Lengend Snippet: FFAs do not affect the desmin expression pattern in human primary myoblasts. ( a ) SkMs were treated with FAs conjugated with BSA or BSA alone (control) before DAPI and desmin staining. ( b ) Fluorescence images from 3 sets of experiments were analyzed, as described in the legend to . The number of DAPI-positive FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The data are presented as the mean ± SD of cell number (dotted bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*). p ≤ 0.01 (**).

Article Snippet: Primary human skeletal muscle myoblasts (SkMs) were obtained from Lonza, Basel, Switzerland (CC-2561).

Techniques: Expressing, Control, Staining, Fluorescence, Comparison

FFAs are differentially utilized in human primary myoblasts. ( a ) SkMs were treated with FAs conjugated with BSA or BSA alone (control) for 48 h and stained using BODIPY. ( b ) Fluorescence images from 3 sets of experiments were analyzed as described in the legend to . The fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of relative lipid accumulation (hatched gray bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*).

Journal: Biology

Article Title: Free Fatty Acid Species Differentially Modulate the Inflammatory Gene Response in Primary Human Skeletal Myoblasts

doi: 10.3390/biology10121318

Figure Lengend Snippet: FFAs are differentially utilized in human primary myoblasts. ( a ) SkMs were treated with FAs conjugated with BSA or BSA alone (control) for 48 h and stained using BODIPY. ( b ) Fluorescence images from 3 sets of experiments were analyzed as described in the legend to . The fluorescence intensity of FFA-treated cells was compared to that of control cells, which was set to 1 (c, dashed gray line). The results are presented as the mean ± SD of relative lipid accumulation (hatched gray bars). Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*).

Article Snippet: Primary human skeletal muscle myoblasts (SkMs) were obtained from Lonza, Basel, Switzerland (CC-2561).

Techniques: Control, Staining, Fluorescence, Comparison

FFAs selectively activate RTK phosphorylation in human primary myoblasts. SkMs were treated with FAs conjugated with BSA or BSA alone for two hours. Whole-cell lysates were prepared and each incubated with a single RTK array. Following incubation steps, the slides were washed, imaged and analyzed using a laser scanner. Fluorescence images were processed and analyzed simultaneously using analysis software. To obtain the relative phosphorylation (black bars) of individual RTKs indicated at the top of each diagram, integrated signal intensities from FFA-treated cells were compared to that from control cells, which was set to 1 ( a – g , dashed gray line). Data are presented as the mean ± SD of the relative phosphorylation. Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*). p ≤ 0.01 (**).

Journal: Biology

Article Title: Free Fatty Acid Species Differentially Modulate the Inflammatory Gene Response in Primary Human Skeletal Myoblasts

doi: 10.3390/biology10121318

Figure Lengend Snippet: FFAs selectively activate RTK phosphorylation in human primary myoblasts. SkMs were treated with FAs conjugated with BSA or BSA alone for two hours. Whole-cell lysates were prepared and each incubated with a single RTK array. Following incubation steps, the slides were washed, imaged and analyzed using a laser scanner. Fluorescence images were processed and analyzed simultaneously using analysis software. To obtain the relative phosphorylation (black bars) of individual RTKs indicated at the top of each diagram, integrated signal intensities from FFA-treated cells were compared to that from control cells, which was set to 1 ( a – g , dashed gray line). Data are presented as the mean ± SD of the relative phosphorylation. Statistical significance was calculated using one-way ANOVA with Bonferroni’s multiple comparison test. p ≤ 0.05 (*). p ≤ 0.01 (**).

Article Snippet: Primary human skeletal muscle myoblasts (SkMs) were obtained from Lonza, Basel, Switzerland (CC-2561).

Techniques: Phospho-proteomics, Incubation, Fluorescence, Software, Control, Comparison