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Invitrogen
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The antibody detects a 135 kDa* protein corresponding to mDia2 in immunoblots of human A7r5 and mouse C2C12 cells treated with calyculin A. The antibody detects transfected mDia2 after treatment with calyculin A, but this reactivity is removed after phosphatase treatment. In addition, the antibody does not detect mDia2 (T1061A) mutant.
This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: diaphanous homolog 3; diaphanous-related formin; diaphanous-related formin 3; Diaphanous-related formin-3; DKFZp434C0931; DKFZp686A13178; DRF3; FLJ34705; MDia2; p134mDIA2; Protein diaphanous homolog 3
基因别名: 4930417P13Rik; AN; AUNA1; DIA2; DIAP3; DIAPH3; DRF3; mDia2; mKIAA4117; NSDAN; p134MDia2
UniProt ID: (Human) Q9NSV4, (Mouse) Q9Z207, (Rat) F1LVW7
Entrez Gene ID: (Human) 81624, (Mouse) 56419, (Rat) 290396