Browse our anti-Actin (ACTA1) Antibodies

On are 214 Actin, alpha 1, Skeletal Muscle (ACTA1) Antibodies from 22 different suppliers available. Additionally we are shipping Actin Kits (39) and Actin Proteins (27) and many more products for this protein. A total of 288 Actin products are currently listed.
AA959943, ACTA, Acta-2, Acts, Actsk-1, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3
list all antibodies Gene Name GeneID UniProt
ACTA1 58 P68133
ACTA1 11459 P68134
Anti-Rat ACTA1 ACTA1 29437 P68136

Most Popular Reactivities for anti-Actin (ACTA1) Antibodies

anti-Human Actin Antibodies:

anti-Mouse (Murine) Actin Antibodies:

anti-Rat (Rattus) Actin Antibodies:

All available anti-Actin Antibodies

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More Antibodies against Actin Interaction Partners

Human Actin, alpha 1, Skeletal Muscle (ACTA1) interaction partners

  1. 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.

  2. 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.

  3. 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.

  4. Upon actin engagement, the N-terminal "strap" and helix 1 are displaced from the vinculin tail helical bundle to mediate actin bundling.

  5. This study reported the new information on the frequency and phenotypes of congenital myopathy caused by ACTA1 mutations in subjects >/=5 years of age.

  6. 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.

  7. Mutations in ACTA1 can cause pathologic features consistent with myofibrillar myopathy.

  8. TIMP-1 (show TIMP1 Antibodies) significantly increased levels of alpha-SMA (show SMN1 Antibodies).

  9. Myopathy associated with zebra bodies is part of the spectrum of myopathies associated with the ACTA1 gene.

  10. New scapuloperoneal phenotype associated with an ACTA1 mutation.

Pig (Porcine) Actin, alpha 1, Skeletal Muscle (ACTA1) interaction partners

  1. Titin-actin interaction: PEVK-actin-based viscosity in a large animal.

Mouse (Murine) Actin, alpha 1, Skeletal Muscle (ACTA1) interaction partners

  1. alpha smooth muscle actin (show ACTG2 Antibodies) (alphaSMA (show ACTA2 Antibodies)) was identified as a marker of osteoprogenitor cells in bone and periodontium.

  2. WIP is a link between membrane lipid composition and actin cytoskeleton at dendritic spines.

  3. ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism.

  4. 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.

  5. Data indicate roles for linkers of nucleus to cytoskeleton (LINC) molecules nesprin2giant and nesprin3, which anchor actin cap fibers to the nucleus.

  6. 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.

  7. 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.

  8. 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.

  9. Results provide the genetic proof that platelet production from megakaryocytes strictly requires dynamic changes in the actin cytoskeleton.

  10. 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.

Actin (ACTA1) Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with Actin (ACTA1)

  • actin, alpha 1, skeletal muscle (ACTA1) antibody
  • actin, alpha 1, skeletal muscle (Acta1) antibody
  • actin, muscle (LOC100533357) antibody
  • AA959943 antibody
  • ACTA antibody
  • Acta-2 antibody
  • Acts antibody
  • Actsk-1 antibody
  • ASMA antibody
  • CFTD antibody
  • CFTD1 antibody
  • CFTDM antibody
  • MPFD antibody
  • NEM1 antibody
  • NEM2 antibody
  • NEM3 antibody

Protein level used designations for ACTA1

actin, alpha 1, skeletal muscle , actin, alpha skeletal muscle , nemaline myopathy type 3 , alpha actin 1 , alpha-actin-1 , skeletal alpha actin , actin alpha 1 , a-actin

100609865 Pan troglodytes
58 Homo sapiens
100154254 Sus scrofa
281592 Bos taurus
11459 Mus musculus
29437 Rattus norvegicus
100716933 Cavia porcellus
421534 Gallus gallus
100533357 Aplysia californica
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