Gene: SPAG17
Official Full Name: sperm associated antigen 17provided by HGNC
Gene Summary: This gene encodes a central pair protein present in the axonemes of cells with a "9 + 2" organization of microtubules. The encoded protein is required for the proper function of the axoneme. Mutations in the orthologous gene in mice lead to primary ciliary dyskinesia characterized by immotile nasal and tracheal cilia, reduced clearance of nasal mucus, profound respiratory distress, hydrocephalus, and neonatal lethality within twelve hours of birth due to impaired airway mucociliary clearance. Single-nucleotide polymorphisms in this gene are associated with human height and targeted mutations lead to skeletal malformations affecting the limbs in mice, suggesting a role for this gene in skeletal development. [provided by RefSeq, Feb 2017]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA04027 | SPAG17 Knockout cell line (AC16) | Human | SPAG17 | 1:3-1:4 | negative | Online Inquiry |
| KOA19471 | SPAG17 Knockout cell line (BEAS-2B) | Human | SPAG17 | 1:3~1:4 | negative | Online Inquiry |
| KOA34923 | SPAG17 Knockout cell line (U-2932) | Human | SPAG17 | 1:2-1:4 | negative | Online Inquiry |
| KOA50327 | SPAG17 Knockout cell line (TPC-1) | Human | SPAG17 | 1:5-1:8 | negative | Online Inquiry |
| KOA65732 | SPAG17 Knockout cell line (NCM460) | Human | SPAG17 | 1:2~1:3 | negative | Online Inquiry |
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