anti-Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3) Anticorps

Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. De plus, nous expédions Myosin Heavy Chain 3, Skeletal Muscle, Embryonic Protéines (6) et Myosin Heavy Chain 3, Skeletal Muscle, Embryonic Kits (4) et beaucoup plus de produits pour cette protéine.

afficher tous les anticorps Gène GeneID UniProt
MYH3 4621 P11055
MYH3 24583 P12847
MYH3 17883 P13541
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Top anti-Myosin Heavy Chain 3, Skeletal Muscle, Embryonic Anticorps sur anticorps-enligne.fr

Showing 10 out of 34 products:

Catalogue No. Reactivité Hôte Conjugué Application Images Quantité Livraison Prix Détails
Humain Lapin Inconjugué ELISA, WB Western blot analysis of MYH3 using mouse brain lysates Western blot analysis of extracts from Hela, using MYH3 Antibody. Lane 1 was treated with the blocking peptide. 100 μL 11 to 12 Days
$390.77
Détails
Humain Lapin Inconjugué ICC, IHC, WB Figure.DAB staining on IHC-P. Samples: Human Tissue 100 μg 13 to 16 Days
$350.00
Détails
Rat Lapin Inconjugué ICC, IHC, WB Figure.DAB staining on IHC-P. Samples: Rat Tissue 100 μg 13 to 16 Days
$380.00
Détails
Humain Lapin Inconjugué ELISA, WB   100 μL 11 to 13 Days
$335.04
Détails
Humain Lapin Inconjugué ELISA, IHC (p), WB   0.1 mg 2 to 3 Days
$360.00
Détails
Humain Souris Inconjugué ELISA, WB   100 μg 11 to 14 Days
$551.83
Détails
Humain Lapin Inconjugué WB   100 μL 11 to 14 Days
$390.50
Détails
Rat Lapin Inconjugué WB   100 μL 11 to 14 Days
$405.17
Détails
Humain Lapin Inconjugué ELISA, WB   100 μg 1 to 2 Days
$394.90
Détails
Rat Lapin Biotin WB   100 μL 11 to 14 Days
$419.83
Détails

Plus d’anticorps contre Myosin Heavy Chain 3, Skeletal Muscle, Embryonic partenaires d’interaction

Human Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3) interaction partners

  1. two heterozygous variations of the MYH3 gene probably underlie the disease in the pedigrees

  2. Our findings also support a role for MYH3 in both muscle and bone development, suggesting a phenotypic continuum in MYH3-related disorders.

  3. Although some MYH3 variants cause dominant Spondylocarpotarsal synostosis syndrome, these data indicate that others (notably truncating variants) do not, except in the context of compound heterozygosity for a second hypomorphic allele.

  4. A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination.

  5. Our findings demonstrate that dominant mutations in MYH3 underlie autosomal dominant SCT, identify a postnatal role for embryonic myosin and suggest that altered regulation of signal transduction in the muscles within the spine may lead to the development of vertebral fusions.

  6. our patient is the first reported case of a child with classical FSS, caused by a common MYH3 mutation, who has an unaffected mother with molecularly proven somatic mosaicism, who is also a likely gonadal mosaic. This case emphasizes the importance of parental genetic testing, when a clinically apparent de novo diagnosis is suspected in a child.

  7. Protein-altering variants of MYH3 were identified in two families with symptoms related to autosomal dominant spondylocarpotarsal synostosis syndrome.

  8. MYH3 mutations are associated with Freeman-Sheldon Syndrome.

  9. developmental p.Thr178Ile MYH3 myopathy is associated with a combined pathomechanism of insufficient dosage of functional embryonic MyHC and production of mutant protein

  10. The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle

  11. The phenotypic overlap among persons with MPS, coupled with physical findings distinct from other conditions caused by mutations in MYH3.

  12. Molecular genetic investigations revealed pathogenic mutations in MYH3, TPM2, and TNNI2 in one sporadic and 19 familial cases of distal arthrogryposis.

  13. eMYH plays a crucial role in important processes in the early developing heart and, hence, is a candidate causative gene for atrial septal defects and cardiomyopathy.

  14. Identification of an MYH3 mutation in this family with distal arthrogryposis type 1 broadens the phenotype associated with MYH3 mutations to include distal arthrogryposis types 1, 2A (Freeman-Sheldon syndrome), and 2B (Sheldon-Hall syndrome).

  15. show that mutations in the embryonic myosin heavy chain 3 gene cause Freeman-Sheldon syndrome, one of the most severe multiple congenital contracture syndromes, and nearly 1/3 of all cases of Sheldon-Hall syndrome, the most common distal arthrogryposis

  16. This article reports novel MYH3 mutations associated with distal arthrogryposis and demonstrates myopathic changes in muscle biopsy specimens from 4 patients with distal arthrogryposis and MYH3 mutations.

  17. Skeletal muscle contractile gene (TNNT3, MYH3, TPM2) mutations not found in vertical talus or clubfoot.

Cow (Bovine) Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3) interaction partners

  1. the result of the study proved that polymorphisms in MYH3 gene are associated with the growth performance of Chinese Qinchuan cattle.

  2. The results showed that some MYH3 genotypes had a significant effect on the growth and carcass traits.

Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3) profil antigène

Profil protéine

Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome.

Gene names and symbols associated with MYH3

  • myosin heavy chain 3 (MYH3) anticorps
  • myosin heavy chain 3 (Myh3) anticorps
  • myosin, heavy polypeptide 3, skeletal muscle, embryonic (Myh3) anticorps
  • Myosin-3 (myo-3) anticorps
  • myosin, heavy chain 3, skeletal muscle, embryonic (MYH3) anticorps
  • HEMHC anticorps
  • MHC A anticorps
  • MyHC-emb anticorps
  • Myhs-e anticorps
  • Myhse anticorps
  • MYHSE1 anticorps
  • RNMHCG anticorps
  • SMHCE anticorps

Protein level used designations for MYH3

myosin heavy chain, fast skeletal muscle, embryonic , myosin, heavy polypeptide 3, skeletal muscle, embryonic , myosin, skeletal, heavy chain, embryonic 1 , myosin-3 , myosin heavy chain 3 , myosin heavy polypeptide 3 , embryonic skeletal myosin heavy chain isoform , Myosin heavy chain A , embryonic myosin heavy chain , embryonic/neonatal myosin heavy chain

GENE ID SPECIES
4621 Homo sapiens
24583 Rattus norvegicus
17883 Mus musculus
179676 Caenorhabditis elegans
100009406 Oryctolagus cuniculus
281338 Bos taurus
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