TLN2 Polyclonal Antibody, 50ul Plasmid Preparation Mutations in this gene are

Mutations in this gene are the cause of infantile-onset STING-associated vasculopathy

The autoproteolytic processing of the caspases in the complex triggers a downstream caspase cascade

It is involved in fibrillar network organization| the anchoring of otoconial membranes and cupulae to the neuroepithelia| and likely in sound stimulation resistance

a helicase ATP-binding domain and an additional functional domain

the encoded protein can be a transcriptional activator or repressor

TLN2 Polyclonal Antibody, 50ul Plasmid Preparation Mutations in this gene areThis gene encodes a protein related to talin 1, a cytoskeletal protein that plays a significant role in the assembly of actin filaments and in spreading and migration of various cell types, including fibroblasts and osteoclasts. This protein has a different pattern of expression compared to talin 1 but, like talin 1, is thought to associate with unique transmembrane receptors to form novel linkages between extracellular matrices and the actin