Gene-specific Copy Number Variation Probe-FLNA
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| Catalog: |
CNVFP-FLNA-05426 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FLNA). 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: |
FLNA Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FLNA genes. This product achieves the purpose of detection by hybridizing with the FLNA 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 |
Filamin A |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009] |
| Gene Symbol |
FLNA |
| Location |
Xq28 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 153576899-153603006 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-FLNA-05426-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FLNA-05426-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FLNA-05426-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FLNA-05426-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FLNA-05426-AQ |
467nm |
418nm |
|
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