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 |
|---|---|---|---|---|
| SEPT1BA-20-REGO | 20 (40 μL) | 200 μL |
|
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| SEPT1BA-20-REGR | 20 (40 μL) | 200 μL |
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| SEPT1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SEPT1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SEPT1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SEPT1BA-20-GROR | 20 (40 μL) | 200 μL |
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| SEPT1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SEPT1BA-20-AQOR | 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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