Gene-specific Copy Number Variation Probe-FOXP2
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| Catalog: |
CNVFP-FOXP2-05597 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FOXP2). 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: |
FOXP2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FOXP2 genes. This product achieves the purpose of detection by hybridizing with the FOXP2 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 |
Forkhead Box P2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010] |
| Gene Symbol |
FOXP2 |
| Location |
7q31.1 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 113726364-114333827 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-FOXP2-05597-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FOXP2-05597-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FOXP2-05597-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FOXP2-05597-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FOXP2-05597-AQ |
467nm |
418nm |
|
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