ALK Polyclonal Antibody, 20ul[BT-AP00370] Monoclonal Antibodies ALK/TPM4 (chromosome 19)

ALK/TPM4 (chromosome 19)

Mutations in this gene cause combined oxidative phosphorylation deficiency 6 (COXPD6)

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Monoclonal antibody sequencing includes hybridoma cell line sequencing and clonal B cell sequencing

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ALK Polyclonal Antibody, 20ul[BT-AP00370] Monoclonal Antibodies ALK/TPM4 (chromosome 19)ALK encodes a receptor tyrosine kinase, which belongs to the insulin receptor superfamily. ALK tyrosine kinase receptor comprises an extracellular domain, an hydrophobic stretch corresponding to a single pass transmembrane region, and an intracellular kinase domain. It plays an important role in the development of the brain and exerts its effects on specific neurons in the nervous system. This gene has been found to be rearranged, mutated, or