anti pard3 Search Results


94
Bio-Techne corporation pard3/par3 antibody
Pard3/Par3 Antibody, supplied by Bio-Techne corporation, 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/anti+pard3/PARD3%2FPar3+Antibody/custom%40nbp1-88861%4032294451
Average 94 stars, based on 1 article reviews
pard3/par3 antibody - by Bioz Stars, 2026-09
94/100 stars
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90
Merck KGaA rabbit anti pard3 07-330
Lack of PKCθ stimulates symmetric self-renewal by regulating <t>Pard3</t> polarization. ( A ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 48h in culture. Myofibers were stained for Pax7 (red) and MyoD (green), nuclei were counterstained with Topro3. ( B ): Quantification of symmetric division events. ( C ): Quantification of Pax7 + /MyoD − cell doublets, and ( D ): quantification of total Pax7 + /MyoD − cells in WT and PKCθ-/- single myofibers. ( E ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 36h in culture. Myofibers were stained for Pax7 (red) and Pard3 (green), nuclei were counterstained with Topro3. ( F ): Percentage ofSCs showing symmetric, low or asymmetric Pard3 distribution in WT and PKCθ-/- myofibers. ( G ): Percentage of SCs showing symmetric and asymmetric Pard3 distribution (WT, n = 3 mice, PKCθ-/-, n = 3 mice, n > 20 myofibers analyzed per mouse). Error bars represent mean ± sem, * p < 0.05 calculated by Student’s t -test.
Rabbit Anti Pard3 07 330, 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/product/anti+pard3/antibody+rabbit+anti+pard3/pmc07177808-188-18-20
Average 90 stars, based on 1 article reviews
rabbit anti pard3 07-330 - by Bioz Stars, 2026-09
90/100 stars
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94
Atlas Antibodies anti par 3 antibody
Lack of PKCθ stimulates symmetric self-renewal by regulating <t>Pard3</t> polarization. ( A ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 48h in culture. Myofibers were stained for Pax7 (red) and MyoD (green), nuclei were counterstained with Topro3. ( B ): Quantification of symmetric division events. ( C ): Quantification of Pax7 + /MyoD − cell doublets, and ( D ): quantification of total Pax7 + /MyoD − cells in WT and PKCθ-/- single myofibers. ( E ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 36h in culture. Myofibers were stained for Pax7 (red) and Pard3 (green), nuclei were counterstained with Topro3. ( F ): Percentage ofSCs showing symmetric, low or asymmetric Pard3 distribution in WT and PKCθ-/- myofibers. ( G ): Percentage of SCs showing symmetric and asymmetric Pard3 distribution (WT, n = 3 mice, PKCθ-/-, n = 3 mice, n > 20 myofibers analyzed per mouse). Error bars represent mean ± sem, * p < 0.05 calculated by Student’s t -test.
Anti Par 3 Antibody, supplied by Atlas Antibodies, 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/anti+pard3/Anti-PARD3/pm28188749-60-7-12
Average 94 stars, based on 1 article reviews
anti par 3 antibody - by Bioz Stars, 2026-09
94/100 stars
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N/A
Rabbit anti-Human PARD3 Polyclonal Antibody
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N/A
Recombinant Mouse Antibody scFv Fragment recognizes and reacts with Human PARD3, expressed in E. coli.Formats of immunological tests: Western blot; Neutralization; Functional StudyStore at 4°C for up to 3 months. For longer term storage aliquot
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N/A
Rabbit anti-Human PARD3 Polyclonal Antibody
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PARD3 / PAR3 Rabbit anti-Human Polyclonal (C-Terminus) (Unconjugated) Antibody, (50 µg)
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Rabbit Anti-PARD3 Antibody, (100 µg)
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N/A
Adapter protein involved in asymmetrical cell division and cell polarization processes. Seems to play a central role in the formation of epithelial tight junctions. Targets the phosphatase PTEN to cell junctions (By similarity). Association with
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Image Search Results


Lack of PKCθ stimulates symmetric self-renewal by regulating Pard3 polarization. ( A ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 48h in culture. Myofibers were stained for Pax7 (red) and MyoD (green), nuclei were counterstained with Topro3. ( B ): Quantification of symmetric division events. ( C ): Quantification of Pax7 + /MyoD − cell doublets, and ( D ): quantification of total Pax7 + /MyoD − cells in WT and PKCθ-/- single myofibers. ( E ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 36h in culture. Myofibers were stained for Pax7 (red) and Pard3 (green), nuclei were counterstained with Topro3. ( F ): Percentage ofSCs showing symmetric, low or asymmetric Pard3 distribution in WT and PKCθ-/- myofibers. ( G ): Percentage of SCs showing symmetric and asymmetric Pard3 distribution (WT, n = 3 mice, PKCθ-/-, n = 3 mice, n > 20 myofibers analyzed per mouse). Error bars represent mean ± sem, * p < 0.05 calculated by Student’s t -test.

Journal: International Journal of Molecular Sciences

Article Title: Targeting PKCθ Promotes Satellite Cell Self-Renewal

doi: 10.3390/ijms21072419

Figure Lengend Snippet: Lack of PKCθ stimulates symmetric self-renewal by regulating Pard3 polarization. ( A ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 48h in culture. Myofibers were stained for Pax7 (red) and MyoD (green), nuclei were counterstained with Topro3. ( B ): Quantification of symmetric division events. ( C ): Quantification of Pax7 + /MyoD − cell doublets, and ( D ): quantification of total Pax7 + /MyoD − cells in WT and PKCθ-/- single myofibers. ( E ): Representative pictures of single myofibers isolated from EDL muscles of WT and PKCθ-/- mice, after 36h in culture. Myofibers were stained for Pax7 (red) and Pard3 (green), nuclei were counterstained with Topro3. ( F ): Percentage ofSCs showing symmetric, low or asymmetric Pard3 distribution in WT and PKCθ-/- myofibers. ( G ): Percentage of SCs showing symmetric and asymmetric Pard3 distribution (WT, n = 3 mice, PKCθ-/-, n = 3 mice, n > 20 myofibers analyzed per mouse). Error bars represent mean ± sem, * p < 0.05 calculated by Student’s t -test.

Article Snippet: Primary antibodies mouse anti Pax7, rabbit anti-MyoD (1:50 Santa Cruz C20: sc-304, Dallas, TX, USA), and rabbit anti Pard3 (07-330 Merck Millipore, Burlington, MA, USA) were incubated O/N at 4 °C.

Techniques: Isolation, Staining