Gene-specific Copy Number Variation Probe-SPAG17
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| Catalog: |
CNVFP-SPAG17-19804 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPAG17). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
SPAG17 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPAG17 genes. This product achieves the purpose of detection by hybridizing with the SPAG17 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Sperm Associated Antigen 17 |
| Gene Summary [Provided by RefSeq] |
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] |
| Gene Symbol |
SPAG17 |
| Location |
1p12 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 118496287-118727848 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-SPAG17-19804-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SPAG17-19804-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SPAG17-19804-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SPAG17-19804-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SPAG17-19804-AQ |
467nm |
418nm |
|
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