This gene encodes a member of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with and negatively regulates the heterodimeric capping protein and promotes cell migration. Reduced expression of this gene has been observed in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized by smooth muscle tumors and impaired T-cell function. [provided by RefSeq, May 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CARMIL2-20-RE | 20 (40 μL) | 200 μL |  |
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| CARMIL2-20-OR | 20 (40 μL) | 200 μL |  |
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| CARMIL2-20-GO | 20 (40 μL) | 200 μL |  |
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| CARMIL2-20-GR | 20 (40 μL) | 200 μL |  |
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| CARMIL2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with and negatively regulates the heterodimeric capping protein and promotes cell migration. Reduced expression of this gene has been observed in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized by smooth muscle tumors and impaired T-cell function. [provided by RefSeq, May 2017]
Gene Symbol : CARMIL2
Gene Name : Capping protein regulator and myosin 1 linker 2
Chromosome : CHR 16: 676,450,03-676,575,68
Locus : 16q22.1
Alt. Genes : CEBPZ
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