Gene-specific Copy Number Variation Probe-TCF4
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| Catalog: |
CNVFP-TCF4-20678 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TCF4). 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: |
TCF4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TCF4 genes. This product achieves the purpose of detection by hybridizing with the TCF4 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 |
Transcription Factor 4 |
| Gene Summary [Provided by RefSeq] |
This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Jul 2016] |
| Gene Symbol |
TCF4 |
| Location |
18q21.2 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 52889561-53303188 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-TCF4-20678-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TCF4-20678-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TCF4-20678-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TCF4-20678-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TCF4-20678-AQ |
467nm |
418nm |
|
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