Gene-specific Copy Number Variation Probe-IFT74
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| Catalog: |
CNVFP-IFT74-07084 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (IFT74). 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: |
IFT74 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to IFT74 genes. This product achieves the purpose of detection by hybridizing with the IFT74 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 |
Intraflagellar Transport 74 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a core intraflagellar transport (IFT) protein which belongs to a multi-protein complex involved in the transport of ciliary proteins along axonemal microtubules. IFT proteins are found at the base of the cilium as well as inside the cilium, where they assemble into long arrays between the ciliary base and tip. This protein, together with intraflagellar transport protein 81, binds and transports tubulin within cilia and is required for ciliogenesis. Naturally occurring mutations in this gene are associated with amyotrophic lateral sclerosis--frontotemporal dementia and Bardet-Biedl Syndrome. [provided by RefSeq, Mar 2017] |
| Gene Symbol |
IFT74 |
| Location |
9p21.2 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 26947036-27062931 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-IFT74-07084-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-IFT74-07084-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-IFT74-07084-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-IFT74-07084-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-IFT74-07084-AQ |
467nm |
418nm |
|
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