myod1 polyclonal antibody Search Results


rabbit anti myod antibody  (Bioss)
93
Bioss rabbit anti myod antibody
Proposed model for SPARCL1 regulation of bovine MDSC migration and differentiation through ITGB1. As an extracellular matrix protein, SPARCL1 interacts with the transmembrane receptor ITGB1 and regulates changes in the expression of adhesion-plaque-associated proteins, such as ITGB1, p-FAK, FAK, p-paxillin, paxillin, and vinculin to affect the formation of focal adhesions. The Cdc42 <t>and</t> <t>Arp2/3</t> complex was also affected by SPARCL1 through ITGB1. Further, bovine MDSC migration was stimulated by SPARCL1, and cells gathered and apparently expressed <t>MyoD</t> to begin an early-stage differentiation.
Rabbit Anti Myod Antibody, supplied by Bioss, 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/result/rabbit anti myod antibody/product/Bioss
Average 93 stars, based on 1 article reviews
rabbit anti myod antibody - by Bioz Stars, 2026-02
93/100 stars
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myod  (OriGene)
90
OriGene myod
Lentivirus production and experiment scheme. (a) Western blot analysis <t>of</t> <t>PPARγ</t> and M3-PPARγ. Human myoblasts were transduced with lenti-GFP, lenti-PPARγ or lenti-M3-, and protein lysates were collected for Western blot by antibodies against <t>MyoD,</t> PPARγ, and β-actin (as a loading control) 48 h post-transduction. (b) Experimental scheme testing for the differentiation of human myoblasts into brown-like adipocytes. Human myoblasts were transduced with the indicated lentiviruses and cultured in induction medium containing IBMX, rosiglitazone, insulin and dexamethasone for 3 days. Then the cells were cultured in differentiation medium without IBMX and rosiglitazone for 8 days before analysis.
Myod, 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/result/myod/product/OriGene
Average 90 stars, based on 1 article reviews
myod - by Bioz Stars, 2026-02
90/100 stars
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myod  (Bioss)
93
Bioss myod
Lentivirus production and experiment scheme. (a) Western blot analysis <t>of</t> <t>PPARγ</t> and M3-PPARγ. Human myoblasts were transduced with lenti-GFP, lenti-PPARγ or lenti-M3-, and protein lysates were collected for Western blot by antibodies against <t>MyoD,</t> PPARγ, and β-actin (as a loading control) 48 h post-transduction. (b) Experimental scheme testing for the differentiation of human myoblasts into brown-like adipocytes. Human myoblasts were transduced with the indicated lentiviruses and cultured in induction medium containing IBMX, rosiglitazone, insulin and dexamethasone for 3 days. Then the cells were cultured in differentiation medium without IBMX and rosiglitazone for 8 days before analysis.
Myod, supplied by Bioss, 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/result/myod/product/Bioss
Average 93 stars, based on 1 article reviews
myod - by Bioz Stars, 2026-02
93/100 stars
  Buy from Supplier
rabbit polyclonal antibodies against myogenic differentiation 1 myod1 sab4300397  (Merck KGaA)
90
Merck KGaA rabbit polyclonal antibodies against myogenic differentiation 1 myod1 sab4300397
Lentivirus production and experiment scheme. (a) Western blot analysis <t>of</t> <t>PPARγ</t> and M3-PPARγ. Human myoblasts were transduced with lenti-GFP, lenti-PPARγ or lenti-M3-, and protein lysates were collected for Western blot by antibodies against <t>MyoD,</t> PPARγ, and β-actin (as a loading control) 48 h post-transduction. (b) Experimental scheme testing for the differentiation of human myoblasts into brown-like adipocytes. Human myoblasts were transduced with the indicated lentiviruses and cultured in induction medium containing IBMX, rosiglitazone, insulin and dexamethasone for 3 days. Then the cells were cultured in differentiation medium without IBMX and rosiglitazone for 8 days before analysis.
Rabbit Polyclonal Antibodies Against Myogenic Differentiation 1 Myod1 Sab4300397, supplied by Merck KGaA, 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/rabbit polyclonal antibodies against myogenic differentiation 1 myod1 sab4300397/product/Merck KGaA
Average 90 stars, based on 1 article reviews
rabbit polyclonal antibodies against myogenic differentiation 1 myod1 sab4300397 - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier
anti myod  (Bioss)
94
Bioss anti myod
Lentivirus production and experiment scheme. (a) Western blot analysis <t>of</t> <t>PPARγ</t> and M3-PPARγ. Human myoblasts were transduced with lenti-GFP, lenti-PPARγ or lenti-M3-, and protein lysates were collected for Western blot by antibodies against <t>MyoD,</t> PPARγ, and β-actin (as a loading control) 48 h post-transduction. (b) Experimental scheme testing for the differentiation of human myoblasts into brown-like adipocytes. Human myoblasts were transduced with the indicated lentiviruses and cultured in induction medium containing IBMX, rosiglitazone, insulin and dexamethasone for 3 days. Then the cells were cultured in differentiation medium without IBMX and rosiglitazone for 8 days before analysis.
Anti Myod, supplied by Bioss, 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/anti myod/product/Bioss
Average 94 stars, based on 1 article reviews
anti myod - by Bioz Stars, 2026-02
94/100 stars
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tnni1  (Bioss)
90
Bioss tnni1
Lentivirus production and experiment scheme. (a) Western blot analysis <t>of</t> <t>PPARγ</t> and M3-PPARγ. Human myoblasts were transduced with lenti-GFP, lenti-PPARγ or lenti-M3-, and protein lysates were collected for Western blot by antibodies against <t>MyoD,</t> PPARγ, and β-actin (as a loading control) 48 h post-transduction. (b) Experimental scheme testing for the differentiation of human myoblasts into brown-like adipocytes. Human myoblasts were transduced with the indicated lentiviruses and cultured in induction medium containing IBMX, rosiglitazone, insulin and dexamethasone for 3 days. Then the cells were cultured in differentiation medium without IBMX and rosiglitazone for 8 days before analysis.
Tnni1, supplied by Bioss, 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/tnni1/product/Bioss
Average 90 stars, based on 1 article reviews
tnni1 - by Bioz Stars, 2026-02
90/100 stars
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Image Search Results


Proposed model for SPARCL1 regulation of bovine MDSC migration and differentiation through ITGB1. As an extracellular matrix protein, SPARCL1 interacts with the transmembrane receptor ITGB1 and regulates changes in the expression of adhesion-plaque-associated proteins, such as ITGB1, p-FAK, FAK, p-paxillin, paxillin, and vinculin to affect the formation of focal adhesions. The Cdc42 and Arp2/3 complex was also affected by SPARCL1 through ITGB1. Further, bovine MDSC migration was stimulated by SPARCL1, and cells gathered and apparently expressed MyoD to begin an early-stage differentiation.

Journal: Animals : an Open Access Journal from MDPI

Article Title: SPARCL1 Influences Bovine Skeletal Muscle-Derived Satellite Cell Migration and Differentiation through an ITGB1-Mediated Signaling Pathway

doi: 10.3390/ani10081361

Figure Lengend Snippet: Proposed model for SPARCL1 regulation of bovine MDSC migration and differentiation through ITGB1. As an extracellular matrix protein, SPARCL1 interacts with the transmembrane receptor ITGB1 and regulates changes in the expression of adhesion-plaque-associated proteins, such as ITGB1, p-FAK, FAK, p-paxillin, paxillin, and vinculin to affect the formation of focal adhesions. The Cdc42 and Arp2/3 complex was also affected by SPARCL1 through ITGB1. Further, bovine MDSC migration was stimulated by SPARCL1, and cells gathered and apparently expressed MyoD to begin an early-stage differentiation.

Article Snippet: Rabbit anti-SPARCL1 antibody (bs-6110R), rabbit anti-integrin beta 1 antibody (bs-0486R), rabbit anti-FAK antibody (bs-20735R), rabbit anti-paxillin antibody (bs-3539R), rabbit anti-phospho-FAK (Tyr397) antibody (bs-3159R), rabbit anti-phospho-paxillin (Tyr118) antibody (bs-3352R), rabbit anti-vinculin antibody (bs-6640R), rabbit anti-ARP2/3 subunit 1B antibody (bs-10563R), rabbit anti-CDC42 antibody (bs-3555R), rabbit anti-MyoD antibody (bs-2442R), rabbit anti-GAPDH antibody (bs-0755R) (all at dilution 1:500; Bioss Antibodies, China).

Techniques: Migration, Expressing

Lentivirus production and experiment scheme. (a) Western blot analysis of PPARγ and M3-PPARγ. Human myoblasts were transduced with lenti-GFP, lenti-PPARγ or lenti-M3-, and protein lysates were collected for Western blot by antibodies against MyoD, PPARγ, and β-actin (as a loading control) 48 h post-transduction. (b) Experimental scheme testing for the differentiation of human myoblasts into brown-like adipocytes. Human myoblasts were transduced with the indicated lentiviruses and cultured in induction medium containing IBMX, rosiglitazone, insulin and dexamethasone for 3 days. Then the cells were cultured in differentiation medium without IBMX and rosiglitazone for 8 days before analysis.

Journal: Obesity (Silver Spring, Md.)

Article Title: Direct conversion of human myoblasts into brown-like adipocytes by engineered superactive PPARγ

doi: 10.1002/oby.21062

Figure Lengend Snippet: Lentivirus production and experiment scheme. (a) Western blot analysis of PPARγ and M3-PPARγ. Human myoblasts were transduced with lenti-GFP, lenti-PPARγ or lenti-M3-, and protein lysates were collected for Western blot by antibodies against MyoD, PPARγ, and β-actin (as a loading control) 48 h post-transduction. (b) Experimental scheme testing for the differentiation of human myoblasts into brown-like adipocytes. Human myoblasts were transduced with the indicated lentiviruses and cultured in induction medium containing IBMX, rosiglitazone, insulin and dexamethasone for 3 days. Then the cells were cultured in differentiation medium without IBMX and rosiglitazone for 8 days before analysis.

Article Snippet: Antibodies used were anti-UCP1 antibody (Cat#ab10983, 1:1000, Abcam, Cambridge, MA), PPARγ (Cat#sc-7196, 1:2000,Santa Cruz Biotechnology, Santa Cruz, CA), MyoD (Cat#TA309755, OriGene, Rockville, MD), anti-β-actin antibody (Sigma) and goat anti-rabbit IgG (H+L) HRP conjugate (Bio-Rad Laboratories, Hercules, CA).

Techniques: Western Blot, Transduction, Cell Culture