Gene-specific Copy Number Variation Probe-ACTL7B
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| Catalog: |
CNVFP-ACTL7B-00119 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ACTL7B). 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: |
ACTL7B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ACTL7B genes. This product achieves the purpose of detection by hybridizing with the ACTL7B 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 |
Actin Like 7B |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7B), and related gene, ACTL7A, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7B gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. Unlike ACTL7A, the ACTL7B gene is expressed predominantly in the testis, however, its exact function is not known. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
ACTL7B |
| Location |
9q31.3 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 111616868-111618275 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-ACTL7B-00119-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ACTL7B-00119-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ACTL7B-00119-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ACTL7B-00119-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ACTL7B-00119-AQ |
467nm |
418nm |
|
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