Gene-specific Copy Number Variation Probe-KNL1
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| Catalog: |
CNVFP-KNL1-08220 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KNL1). 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: |
KNL1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KNL1 genes. This product achieves the purpose of detection by hybridizing with the KNL1 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 |
Kinetochore Scaffold 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a component of the multiprotein assembly that is required for creation of kinetochore-microtubule attachments and chromosome segregation. The encoded protein functions as a scaffold for proteins that influence the spindle assembly checkpoint during the eukaryotic cell cycle and it interacts with at least five different kinetochore proteins and two checkpoint kinases. In adults, this gene is predominantly expressed in normal testes, various cancer cell lines and primary tumors from other tissues and is ubiquitously expressed in fetal tissues. This gene was originally identified as a fusion partner with the mixed-lineage leukemia (MLL) gene in t(11;15)(q23;q14). Mutations in this gene cause autosomal recessive primary microcephaly-4 (MCPH4). Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described but their biological validity has not been confirmed. [provided by RefSeq, Jan 2013] |
| Gene Symbol |
KNL1 |
| Location |
15q15.1 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 40594011-40664341 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-KNL1-08220-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KNL1-08220-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KNL1-08220-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KNL1-08220-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KNL1-08220-AQ |
467nm |
418nm |
|
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