This gene encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell. The encoded mechanosensing protein contains three vinculin homology domains and undergoes conformational changes in response to cytoskeletal tension, resulting in the reconfiguration of cadherin-actin filament connections. Certain mutations in this gene cause butterfly-shaped pigment dystrophy. [provided by RefSeq, May 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CTNNA1-20-RE | 20 (40 μL) | 200 μL |  |
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| CTNNA1-20-OR | 20 (40 μL) | 200 μL |  |
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| CTNNA1-20-GO | 20 (40 μL) | 200 μL |  |
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| CTNNA1-20-GR | 20 (40 μL) | 200 μL |  |
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| CTNNA1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell. The encoded mechanosensing protein contains three vinculin homology domains and undergoes conformational changes in response to cytoskeletal tension, resulting in the reconfiguration of cadherin-actin filament connections. Certain mutations in this gene cause butterfly-shaped pigment dystrophy. [provided by RefSeq, May 2016]
Gene Symbol : CTNNA1
Gene Name : Catenin alpha 1
Chromosome : CHR 5: 138,753,385-138,935,033
Locus : 5q31.2
Alt. Genes : KIF20A
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