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Human Polyclonal Actin Primary Antibody for IHC (p), WB - ABIN3043519
Wu, Zhang, Tao, Dong: Lipoxin A(4) inhibits transition of epithelial to mesenchymal cells in proximal tubules. in American journal of nephrology 2010
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Human Polyclonal Actin Primary Antibody for IHC (p), WB - ABIN3043518
Cai, Xu, Zhang: Bone marrow stromal cells induce cell cycle arrest in reactive astrocytes in vitro. in Neuroscience letters 2012
Show all 56 Pubmed References
Cow (Bovine) Polyclonal Actin Primary Antibody for ICC, IF - ABIN4278064
Liu, Xu, Zhou, Weir, Chen, Trotman: Human umbilical cord stem cell encapsulation in novel macroporous and injectable fibrin for muscle tissue engineering. in Acta biomaterialia 2012
Show all 3 Pubmed References
Chicken Polyclonal Actin Primary Antibody for IHC (p), IHC - ABIN407578
DeSantiago, Bare, Ke, Sheehan, Solaro, Banach: Functional integrity of the T-tubular system in cardiomyocytes depends on p21-activated kinase 1. in Journal of molecular and cellular cardiology 2013
Show all 2 Pubmed References
Human Monoclonal Actin Primary Antibody for ICC, IF - ABIN267970
Wei, Zhang, Bai, Zhang, Zhao, Li, Zhao: The NF-κB-modulated microRNAs miR-195 and miR-497 inhibit myoblast proliferation by targeting Igf1r, Insr and cyclin genes. in Journal of cell science 2016
Human Polyclonal Actin Primary Antibody for FACS, IF - ABIN658563
Ying, Xie, Bai, Chen, Wang, Zhang, Morishita, Sun, Rajagopalan: Exposure to concentrated ambient particulate matter induces reversible increase of heart weight in spontaneously hypertensive rats. in Particle and fibre toxicology 2015
Our study demonstrates that high ActA level is an independent prognosis factor of survival in cancer patients. More than a basic marker of the severity of the neoplastic disease or of the inflammatory process, ActA seems to influence survival by contributing to the development of cachexia and loss of skeletal muscle mass.
The study confirmed ACTA1 mutations in four patients, including one with intranuclear rods, one with large intracytoplasmic aggregates, and two with nemaline intracytoplasmic rods.
Study shows that clinically severe ACTA1-related myopathy can present with muscle morphological findings suggestive of cytoplasmic body myopathy in the absence of definite nemaline rods.
Shorter than normal thin filament length contributes to the impaired force generation in patients with thin filament myopathy, but only in those who harbor specific mutations in NEB (show NEB Antibodies) or ACTA1.
Over-expression of TNC (show TNC Antibodies), SMA (show SMN1 Antibodies), and vimentin (show VIM Antibodies) were significantly correlated with the lower overall survival in prostate cancer patients.
ANA (show BTG3 Antibodies) and ASMA evaluation in patients with liver transplantation and no history of autoimmune disease has no clinical relevance, since it varies in time and is not related to any risk factors or liver injury. Routine autoimmunity evaluation should be avoided.
Upon actin engagement, the N-terminal "strap" and helix 1 are displaced from the vinculin tail helical bundle to mediate actin bundling.
This study reported the new information on the frequency and phenotypes of congenital myopathy caused by ACTA1 mutations in subjects >/=5 years of age.
The authors propose that Lpd delivers Ena/VASP proteins to growing barbed ends and increases their actin polymerase activity by tethering them to actin filaments.
Mutations in ACTA1 can cause pathologic features consistent with myofibrillar myopathy.
Titin-actin interaction: PEVK-actin-based viscosity in a large animal.
alpha smooth muscle actin (show ACTG2 Antibodies) (alphaSMA (show ACTA2 Antibodies)) was identified as a marker of osteoprogenitor cells in bone and periodontium.
WIP is a link between membrane lipid composition and actin cytoskeleton at dendritic spines.
ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism.
Combined MRI (show C7ORF49 Antibodies) and (3)(1)P-MRS investigations of the ACTA1(H40Y) mouse model of nemaline myopathy show impaired muscle function and altered energy metabolism.
Data indicate roles for linkers of nucleus to cytoskeleton (LINC) molecules nesprin2giant and nesprin3, which anchor actin cap fibers to the nucleus.
Asp286Gly acts as a "poison-protein" and according to the computational analysis it modifies the actin-actin interface. This phenomenon is likely to prevent proper myosin cross-bridge binding.
Data show that upon actin binding, the two domains of utrophin (show UTRN Antibodies) become dramatically separated and ordered, indicating a transition to a single open and extended conformation.
Data indicated that CacyBP/SIP (show CACYBP Antibodies) could simultaneously interact with tubulin (show TUBB Antibodies) and actin, suggesting that CacyBP/SIP (show CACYBP Antibodies) might link actin and tubulin (show TUBB Antibodies) cytoskeletons.
Results provide the genetic proof that platelet production from megakaryocytes strictly requires dynamic changes in the actin cytoskeleton.
Data show that while increases in cardiac and vascular smooth-muscle actin can partially compensate for the lack of skeletal actin in null mice, this is not sufficient to support adequate skeletal muscle growth and/or function.
The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.
actin, alpha 1, skeletal muscle
, actin, alpha skeletal muscle
, nemaline myopathy type 3
, alpha actin 1
, skeletal alpha actin
, actin alpha 1