Search results for skeletal muscle

alpha Skeletal Muscle Actin antibody, Genetex, GTX101362

alpha Skeletal Muscle Actin antibody, Genetex, GTX101920

alpha Skeletal Muscle Actin antibody, Genetex, GTX112860

Troponin I Skeletal Muscle Antibody, Abbexa, abx020870

Troponin I Skeletal Muscle Antibody is a Mouse monoclonal antibody for cardiac markers against Troponin I Skeletal Muscle.

Troponin I Skeletal Muscle Antibody, Abbexa, abx020871

Troponin I Skeletal Muscle Antibody is a Mouse monoclonal antibody for cardiac markers against Troponin I Skeletal Muscle.

Actin, Alpha Skeletal Muscle (ACTA1) Antibody, Abbexa, abx159305

ACTA1 Antibody is a Mouse Monoclonal against ACTA1.

Actin, Alpha Skeletal Muscle (ACTA1) Antibody, Abbexa, abx147942

Actin, Alpha Skeletal Muscle (ACTA1) Antibody is a Rabbit Polyclonal antibody for the detection of ACTA1. Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. The ACTA1 gene encodes skeletal muscle alpha-actin, the principal actin isoform in adult skeletal muscle, which interacts with a variety of proteins to produce the force for muscle contraction. There is only the N-termninal 8 amino acids difference among the actin family members. This antibody is specific to the ACTA1. It does not cross-react with other actin isoforms.

Troponin C, Skeletal Muscle (TNNC2) Antibody, Abbexa, abx375800

Troponin C, Skeletal Muscle (TNNC2) Antibody is a Rabbit Polyclonal antibody against Troponin C, Skeletal Muscle (TNNC2).

Actin, Alpha Skeletal Muscle (ACTA1) Antibody, Abbexa, abx230115

ACTA1-Specific Antibody is a Rabbit Polyclonal against ACTA1-Specific.

Actin, Alpha Skeletal Muscle (ACTA1) Antibody, Abbexa, abx028299

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.