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Myosin Heavy Chain 3, Skeletal Muscle, Embryonic Proteins (MYH3)

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 Kits (4) and many more products for this protein.

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

Showing 6 out of 6 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Rat His tag,T7 tag 100 μg Log in to see 11 to 13 Days
$785.40
Details
HOST_Escherichia coli (E. coli) Human His tag 100 μg Log in to see 11 to 13 Days
$792.00
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
HOST_Escherichia coli (E. coli) Rat Un-conjugated   100 μg Log in to see 9 to 19 Days
$952.01
Details
HOST_Escherichia coli (E. coli) Human Un-conjugated   100 μg Log in to see 9 to 19 Days
$967.75
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 19 Days
$785.40
Details

MYH3 Proteins by Origin and Source

Origin Expressed in Conjugate
Rat (Rattus)

Human , ,
,

More Proteins for Myosin Heavy Chain 3, Skeletal Muscle, Embryonic (MYH3) 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 Proteins), and TNNI2 (show TNNI2 Proteins) 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 Proteins)) mutations not found in vertical talus or clubfoot.

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

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

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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