Gene-specific Copy Number Variation Probe-FKBP1A
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| Catalog: |
CNVFP-FKBP1A-05465 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FKBP1A). 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: |
FKBP1A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FKBP1A genes. This product achieves the purpose of detection by hybridizing with the FKBP1A 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 |
FK506 Binding Protein 1A |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor. It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor. In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed. [provided by RefSeq, Sep 2008] |
| Gene Symbol |
FKBP1A |
| Location |
20p13 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 1349620-1373816 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-FKBP1A-05465-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FKBP1A-05465-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FKBP1A-05465-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FKBP1A-05465-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FKBP1A-05465-AQ |
467nm |
418nm |
|
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