This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SEPT1-20-RE | 20 (40 μL) | 200 μL |  |
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| SEPT1-20-OR | 20 (40 μL) | 200 μL |  |
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| SEPT1-20-GO | 20 (40 μL) | 200 μL |  |
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| SEPT1-20-GR | 20 (40 μL) | 200 μL |  |
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| SEPT1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]
Gene Symbol : SEPT1
Gene Name : Septin 1
Chromosome : CHR 16: 303,828,49-303,781,32
Locus : 16p11.2
Alt. Genes : CEBPZ
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