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MYH14 Polyclonal Antibody, 50ul Purification disease:Defects in CAMTA1 are detected

SKU: 7371245233

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MYH14 Polyclonal Antibody, 50ul Purification disease:Defects in CAMTA1 are detectedMYH14 encodes a member of the myosin superfamily. Myosin 14 represents a conventional non muscle myosin; it should not be confused with the unconventional myosin 14 (MYO14). Myosins are actin dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene result in one form of autosomal dominant hearing impairment. Multiple transcript variants encoding different isoforms

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Description

disease:Defects in CAMTA1 are detected in patients with oligodendroglioma and astrocytoma

The leukocyte immunoglobulin like receptor B5 belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains

endothelial cell growth and migration

This gene encodes a member of the VPS10-related sortilin family of proteins

KCNK15 encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains

MYH14 Polyclonal Antibody, 50ul Purification disease:Defects in CAMTA1 are detectedMYH14 encodes a member of the myosin superfamily. Myosin 14 represents a conventional non muscle myosin; it should not be confused with the unconventional myosin 14 (MYO14). Myosins are actin dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene result in one form of autosomal dominant hearing impairment. Multiple transcript variants encoding different isoforms

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