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Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3) ELISA Kits

Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Additionally we are shipping Myosin Heavy Chain 3, Skeletal Muscle, Embryonic Antibodies (16) and Myosin Heavy Chain 3, Skeletal Muscle, Embryonic Proteins (6) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Rat MYH3 MYH3 24583 P12847
MYH3 4621 P11055
Anti-Mouse MYH3 MYH3 17883 P13541
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Top Myosin Heavy Chain 3, Skeletal Muscle, Embryonic ELISA Kits at antibodies-online.com

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Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.126 ng/mL 0.31-20 ng/mL 96 Tests Log in to see 9 to 11 Days
$736.84
Details

More ELISA Kits for Myosin Heavy Chain 3, Skeletal Muscle, Embryonic Interaction Partners

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

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

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

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

  4. Molecular genetic investigations revealed pathogenic mutations in MYH3, TPM2 (show TPM2 ELISA Kits), and TNNI2 (show TNNI2 ELISA Kits) in one sporadic and 19 familial cases of distal arthrogryposis.

  5. 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).

  6. 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

  7. 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.

  8. Skeletal muscle contractile gene (TNNT3, MYH3, TPM2 (show TPM2 ELISA Kits)) mutations not found in vertical talus or clubfoot.

Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3) Antigen Profile

Antigen Summary

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 1B, skeletal muscle (similar to human myosin, heavy chain 1, skeletal muscle, adult) (MYH1B) antibody
  • myosin, heavy chain 1C, skeletal muscle (similar to human myosin, heavy chain 1, skeletal muscle, adult) (MYH1C) antibody
  • myosin, heavy chain 1F, skeletal muscle (similar to human myosin, heavy chain 1, skeletal muscle, adult) (MYH1F) antibody
  • myosin, heavy chain 3, skeletal muscle, embryonic (Myh3) antibody
  • myosin, heavy chain 3, skeletal muscle, embryonic (MYH3) antibody
  • myosin, heavy polypeptide 3, skeletal muscle, embryonic (Myh3) antibody
  • adult antibody
  • embryonic antibody
  • HEMHC antibody
  • MYH1 antibody
  • MYH2 antibody
  • MYH3 antibody
  • MYH4 antibody
  • MYH8 antibody
  • MyHC-emb antibody
  • Myhs-e antibody
  • Myhse antibody
  • MYHSE1 antibody
  • myosin antibody
  • perinatal antibody
  • RNMHCG antibody
  • SMHCE antibody

Protein level used designations for MYH3

MHC (19 AA) , fast skeletal muscle , heavy chain 1 , heavy chain 3 , heavy polypeptide 1 , heavy polypeptide 2 , myosin heavy chain 3 , myosin heavy chain, fast skeletal muscle, embryonic , myosin, heavy chain 1, skeletal muscle, adult , myosin, heavy chain 2, skeletal muscle, adult , myosin, heavy chain 3, skeletal muscle, embryonic , myosin, heavy chain 4, skeletal muscle , myosin, heavy polypeptide 1, skeletal muscle, adult , myosin, heavy polypeptide 2, skeletal muscle, adult , myosin, heavy polypeptide 4, skeletal muscle , myosin, heavy polypeptide 8, skeletal muscle, perinatal , myosin-3 , skeletal muscle , fast myosin heavy chain , heavy chain 2 , heavy chain 8 , heavy polypeptide 8 , myosin, heavy chain 8, skeletal muscle, perinatal , myosin heavy polypeptide 3 , myosin, heavy polypeptide 3, skeletal muscle, embryonic , myosin, skeletal, heavy chain, embryonic 1 , embryonic skeletal myosin heavy chain isoform

GENE ID SPECIES
374069 Gallus gallus
417310 Gallus gallus
768566 Gallus gallus
24583 Rattus norvegicus
4621 Homo sapiens
17883 Mus musculus
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