This is a Validated Antibody Database (VAD) review about mouse Myh9, based on 25 published articles (read how Labome selects the articles), using Myh9 antibody in all methods. It is aimed to help Labome visitors find the most suited Myh9 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
Myh9 synonym: Fltn; Myhn-1; Myhn1; NMHCIIA; NMMHC-A; NMMHC-IIA; TU72.6; myosin-9; NMHC II-A; NMMHC II-a; cellular myosin heavy chain, type A; flectin; myosin IIA; myosin heavy chain IX; non-muscle myosin heavy chain IIa

BioLegend
rabbit polyclonal (Poly19098)
  • immunocytochemistry; human; 1:200; loading ...; fig s1a
BioLegend Myh9 antibody (BioLegend, 909801) was used in immunocytochemistry on human samples at 1:200 (fig s1a). Sci Rep (2018) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; mouse; loading ...; fig s5j
BioLegend Myh9 antibody (Covance, PRB-440P) was used in immunocytochemistry on mouse samples (fig s5j). Dev Cell (2018) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; human; 1:500; loading ...; fig 5d, 7b
  • western blot; human; 1:1000; loading ...; fig 5b
BioLegend Myh9 antibody (Covance, PRB-440P) was used in immunocytochemistry on human samples at 1:500 (fig 5d, 7b) and in western blot on human samples at 1:1000 (fig 5b). Nat Commun (2018) ncbi
rabbit polyclonal (Poly19098)
  • western blot; human; 1:1000; loading ...; fig 6c
BioLegend Myh9 antibody (Covance, PRB-440P) was used in western blot on human samples at 1:1000 (fig 6c). PLoS ONE (2018) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; dog; loading ...
BioLegend Myh9 antibody (BioLegend, 909801) was used in immunocytochemistry on dog samples . PLoS ONE (2017) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; human; loading ...; fig s8a
BioLegend Myh9 antibody (Covance, PRB-440P) was used in immunocytochemistry on human samples (fig s8a). Mol Biol Cell (2017) ncbi
rabbit polyclonal (Poly19098)
  • western blot; human; loading ...; fig s4a
BioLegend Myh9 antibody (Covance, PRB-440P) was used in western blot on human samples (fig s4a). Oncotarget (2017) ncbi
rabbit polyclonal (Poly19098)
  • western blot; human; 1:1000; loading ...; fig 5c
In order to analyze differential functional effects for rho kinases 1 and 2 at the epithelial zonula adherens, BioLegend Myh9 antibody (Covance, PRB-440P) was used in western blot on human samples at 1:1000 (fig 5c). Mol Biol Cell (2017) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; human; 1:1000; loading ...; fig 1d
  • western blot; human; loading ...; fig 1f
In order to investigate the role of Coronin 1B in regulating the non-muscle myosin II pool, BioLegend Myh9 antibody (Covance, PRB-440P) was used in immunocytochemistry on human samples at 1:1000 (fig 1d) and in western blot on human samples (fig 1f). Cell Cycle (2016) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; human; loading ...; fig 1a
In order to find that mitotic focal adhesions link mitotic cell shape and spindle orientation, BioLegend Myh9 antibody (BioLegends, 909801) was used in immunocytochemistry on human samples (fig 1a). Sci Rep (2016) ncbi
rabbit polyclonal (Poly19098)
  • immunohistochemistry; zebrafish ; 1:100; fig 4
In order to assess the drive of lumen formation via blood flow through inverse membrane blebbing during angiogenesis in vivo, BioLegend Myh9 antibody (Covance, PRB-440P) was used in immunohistochemistry on zebrafish samples at 1:100 (fig 4). Nat Cell Biol (2016) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; human; fig 7a
  • western blot; mouse; 1:1000; fig 1a
In order to determine how nuclear translocation during 3D invasion requires non-muscle myosin IIB, BioLegend Myh9 antibody (Covance, PRB-440P) was used in immunocytochemistry on human samples (fig 7a) and in western blot on mouse samples at 1:1000 (fig 1a). J Cell Biol (2015) ncbi
rabbit polyclonal (Poly19098)
  • immunocytochemistry; human
In order to investigate the role of the actin cytoskeleton of the endothelium in transmigration, BioLegend Myh9 antibody (Covance, PRB-440P) was used in immunocytochemistry on human samples . Mol Biol Cell (2014) ncbi
Abnova
mouse monoclonal (3C7)
  • western blot; mouse; loading ...; fig 4c
Abnova Myh9 antibody (Abnova, H00004627-M01) was used in western blot on mouse samples (fig 4c). J Mol Med (Berl) (2018) ncbi
Invitrogen
rabbit polyclonal
  • immunocytochemistry; Dictyostelium discoideum; 1:100; fig 9
In order to investigate how the cortical actin meshwork in the rear develops, Invitrogen Myh9 antibody (Thermo Scientific, PA5-17025) was used in immunocytochemistry on Dictyostelium discoideum samples at 1:100 (fig 9). Nat Commun (2015) ncbi
GeneTex
rabbit polyclonal
  • immunohistochemistry - frozen section; fruit fly; 1:500; fig 5
  • western blot; fruit fly; 1:1000; fig 5
GeneTex Myh9 antibody (Gene Tex, GTX113236) was used in immunohistochemistry - frozen section on fruit fly samples at 1:500 (fig 5) and in western blot on fruit fly samples at 1:1000 (fig 5). elife (2016) ncbi
Cell Signaling Technology
rabbit polyclonal
  • other; human; loading ...; fig 4c
Cell Signaling Technology Myh9 antibody (Cell Signaling, 5026) was used in other on human samples (fig 4c). Cancer Cell (2018) ncbi
rabbit polyclonal
  • western blot; human; loading ...; fig 9i
Cell Signaling Technology Myh9 antibody (Cell Signaling, 3403) was used in western blot on human samples (fig 9i). J Clin Invest (2017) ncbi
rabbit polyclonal
  • reverse phase protein lysate microarray; human; loading ...; fig st6
In order to characterize the molecular identity of uterine carcinosarcomas., Cell Signaling Technology Myh9 antibody (CST, 5026) was used in reverse phase protein lysate microarray on human samples (fig st6). Cancer Cell (2017) ncbi
rabbit polyclonal
  • western blot; mouse; loading ...; fig s10a
In order to explore the role of TPM4 in platelet biogenesis, Cell Signaling Technology Myh9 antibody (Cell Signalling, 5026) was used in western blot on mouse samples (fig s10a). J Clin Invest (2017) ncbi
rabbit polyclonal
  • western blot; mouse; loading ...; fig 5a
In order to discover that calcium-calmodulin-dependent kinase II is an important regulator of smooth muscle function in angiotensin-II hypertension, Cell Signaling Technology Myh9 antibody (Cell Signaling, 3403) was used in western blot on mouse samples (fig 5a). Vascul Pharmacol (2016) ncbi
rabbit polyclonal
  • immunocytochemistry; human; 10 ug/ml; fig 8
  • immunocytochemistry; mouse; 10 ug/ml; fig 3
  • immunohistochemistry; mouse; fig 3
  • western blot; mouse; 1 ug/ml; fig 3
In order to determine the role of TRPM7 channel function defects and how they deregulate thrombopoiesis through altered cellular Mg(2+) homeostasis and cytoskeletal architecture, Cell Signaling Technology Myh9 antibody (CellSignaling, 3403) was used in immunocytochemistry on human samples at 10 ug/ml (fig 8), in immunocytochemistry on mouse samples at 10 ug/ml (fig 3), in immunohistochemistry on mouse samples (fig 3) and in western blot on mouse samples at 1 ug/ml (fig 3). Nat Commun (2016) ncbi
rabbit polyclonal
  • western blot; human
In order to assess the hypothesis that runners who run consistently have superior metabolic fitness, Cell Signaling Technology Myh9 antibody (Cell Signaling, 3403) was used in western blot on human samples . Dis Markers (2015) ncbi
rabbit polyclonal
  • western blot; human
In order to identify the role of obscurins during breast carcinogenesis, Cell Signaling Technology Myh9 antibody (Cell Signaling Technology, 3403) was used in western blot on human samples . Oncogene (2015) ncbi
rabbit polyclonal
  • immunocytochemistry; human
Cell Signaling Technology Myh9 antibody (Cell Signaling Technology, 3403) was used in immunocytochemistry on human samples . Mol Biol Cell (2014) ncbi
EMD Millipore
rabbit polyclonal
  • immunocytochemistry; mouse; loading ...; fig 5a
  • western blot; mouse; loading ...; fig 5c
EMD Millipore Myh9 antibody (EMD Millipore, ab2974) was used in immunocytochemistry on mouse samples (fig 5a) and in western blot on mouse samples (fig 5c). J Mol Med (Berl) (2018) ncbi
Articles Reviewed
  1. Ciuba K, Hawkes W, Tojkander S, Kogan K, Engel U, Iskratsch T, et al. Calponin-3 is critical for coordinated contractility of actin stress fibers. Sci Rep. 2018;8:17670 pubmed publisher
  2. Schell C, Sabass B, Helmstaedter M, Geist F, Abed A, Yasuda Yamahara M, et al. ARP3 Controls the Podocyte Architecture at the Kidney Filtration Barrier. Dev Cell. 2018;47:741-757.e8 pubmed publisher
  3. Latham S, Ehmke N, Reinke P, Taft M, Eicke D, Reindl T, et al. Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia. Nat Commun. 2018;9:4250 pubmed publisher
  4. Diaz Horta O, Abad C, Cengiz F, Bademci G, Blackwelder P, Walz K, et al. Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientation. J Mol Med (Berl). 2018;96:1227-1238 pubmed publisher
  5. Yasuda Yamahara M, Rogg M, Yamahara K, Maier J, Huber T, Schell C. AIF1L regulates actomyosin contractility and filopodial extensions in human podocytes. PLoS ONE. 2018;13:e0200487 pubmed publisher
  6. Ng P, Li J, Jeong K, Shao S, Chen H, Tsang Y, et al. Systematic Functional Annotation of Somatic Mutations in Cancer. Cancer Cell. 2018;33:450-462.e10 pubmed publisher
  7. Fredriksson Lidman K, Van Itallie C, Tietgens A, Anderson J. Sorbin and SH3 domain-containing protein 2 (SORBS2) is a component of the acto-myosin ring at the apical junctional complex in epithelial cells. PLoS ONE. 2017;12:e0185448 pubmed publisher
  8. Kim J, Kim Y, Kim J, Park D, Bae H, Lee D, et al. YAP/TAZ regulates sprouting angiogenesis and vascular barrier maturation. J Clin Invest. 2017;127:3441-3461 pubmed publisher
  9. Owen L, Adhikari A, Patel M, Grimmer P, Leijnse N, Kim M, et al. A cytoskeletal clutch mediates cellular force transmission in a soft, three-dimensional extracellular matrix. Mol Biol Cell. 2017;28:1959-1974 pubmed publisher
  10. Jeong S, Lim S, Schevzov G, Gunning P, Helfman D. Loss of Tpm4.1 leads to disruption of cell-cell adhesions and invasive behavior in breast epithelial cells via increased Rac1 signaling. Oncotarget. 2017;8:33544-33559 pubmed publisher
  11. Cherniack A, Shen H, Walter V, Stewart C, Murray B, Bowlby R, et al. Integrated Molecular Characterization of Uterine Carcinosarcoma. Cancer Cell. 2017;31:411-423 pubmed publisher
  12. Pleines I, Woods J, Chappaz S, Kew V, Foad N, Ballester Beltrán J, et al. Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia. J Clin Invest. 2017;127:814-829 pubmed publisher
  13. Priya R, Liang X, Teo J, Duszyc K, Yap A, Gomez G. ROCK1 but not ROCK2 contributes to RhoA signaling and NMIIA-mediated contractility at the epithelial zonula adherens. Mol Biol Cell. 2017;28:12-20 pubmed publisher
  14. Prasad A, Ketsawatsomkron P, Nuno D, Koval O, Dibbern M, Venema A, et al. Role of CaMKII in Ang-II-dependent small artery remodeling. Vascul Pharmacol. 2016;87:172-179 pubmed publisher
  15. Priya R, Wee K, Budnar S, Gomez G, Yap A, Michael M. Coronin 1B supports RhoA signaling at cell-cell junctions through Myosin II. Cell Cycle. 2016;15:3033-3041 pubmed
  16. Taneja N, Fenix A, Rathbun L, Millis B, Tyska M, Hehnly H, et al. Focal adhesions control cleavage furrow shape and spindle tilt during mitosis. Sci Rep. 2016;6:29846 pubmed publisher
  17. Li T, Giagtzoglou N, Eberl D, Jaiswal S, Cai T, Godt D, et al. The E3 ligase Ubr3 regulates Usher syndrome and MYH9 disorder proteins in the auditory organs of Drosophila and mammals. elife. 2016;5: pubmed publisher
  18. Stritt S, Nurden P, Favier R, Favier M, Ferioli S, Gotru S, et al. Defects in TRPM7 channel function deregulate thrombopoiesis through altered cellular Mg(2+) homeostasis and cytoskeletal architecture. Nat Commun. 2016;7:11097 pubmed publisher
  19. Gebala V, Collins R, Geudens I, Phng L, Gerhardt H. Blood flow drives lumen formation by inverse membrane blebbing during angiogenesis in vivo. Nat Cell Biol. 2016;18:443-50 pubmed publisher
  20. Ramalingam N, Franke C, Jaschinski E, Winterhoff M, Lu Y, Brühmann S, et al. A resilient formin-derived cortical actin meshwork in the rear drives actomyosin-based motility in 2D confinement. Nat Commun. 2015;6:8496 pubmed publisher
  21. Thomas D, Yenepalli A, Denais C, Rape A, Beach J, Wang Y, et al. Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion. J Cell Biol. 2015;210:583-94 pubmed publisher
  22. Laye M, Nielsen M, Hansen L, Knudsen T, Pedersen B. Physical activity enhances metabolic fitness independently of cardiorespiratory fitness in marathon runners. Dis Markers. 2015;2015:806418 pubmed publisher
  23. Shriver M, Stroka K, Vitolo M, Martin S, Huso D, Konstantopoulos K, et al. Loss of giant obscurins from breast epithelium promotes epithelial-to-mesenchymal transition, tumorigenicity and metastasis. Oncogene. 2015;34:4248-59 pubmed publisher
  24. Mooren O, Li J, Nawas J, Cooper J. Endothelial cells use dynamic actin to facilitate lymphocyte transendothelial migration and maintain the monolayer barrier. Mol Biol Cell. 2014;25:4115-29 pubmed publisher
  25. Mana Capelli S, Paramasivam M, Dutta S, McCollum D. Angiomotins link F-actin architecture to Hippo pathway signaling. Mol Biol Cell. 2014;25:1676-85 pubmed publisher