Gene-specific Copy Number Variation Probe-ARMC4
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| Catalog: |
CNVFP-ARMC4-01018 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ARMC4). 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: |
ARMC4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ARMC4 genes. This product achieves the purpose of detection by hybridizing with the ARMC4 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 |
Armadillo Repeat Containing 4 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene contains ten Armadillo repeat motifs (ARMs) and one HEAT repeat, and is thought to be involved in ciliary and flagellar movement. This protein has been shown to localize to the ciliary axonemes and at the ciliary base of respiratory cells. Studies indicate that mutations in this gene cause partial outer dynein arm (ODA) defects in respiratory cilia. The cilia of cells with mutations in this gene displayed either reduced ciliary beat frequency and amplitude, or, complete immotility. Some individuals with primary ciliary dyskensia (PCD) have been shown to have mutations in this gene. PCD is characterized by chronic airway disease and left/right body asymmetry defects. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
| Gene Symbol |
ARMC4 |
| Location |
10p12.1 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 28101096-28287977 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-ARMC4-01018-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ARMC4-01018-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ARMC4-01018-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ARMC4-01018-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ARMC4-01018-AQ |
467nm |
418nm |
|
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