Gene-specific Copy Number Variation Probe-TGIF1
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| Catalog: |
CNVFP-TGIF1-20570 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TGIF1). 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: |
TGIF1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TGIF1 genes. This product achieves the purpose of detection by hybridizing with the TGIF1 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 |
TGFB Induced Factor Homeobox 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the three-amino acid loop extension (TALE) superclass of atypical homeodomains. TALE homeobox proteins are highly conserved transcription regulators. This particular homeodomain binds to a previously characterized retinoid X receptor responsive element from the cellular retinol-binding protein II promoter. In addition to its role in inhibiting 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element, the protein is an active transcriptional co-repressor of SMAD2 and may participate in the transmission of nuclear signals during development and in the adult. Mutations in this gene are associated with holoprosencephaly type 4, which is a structural anomaly of the brain. Alternative splicing has been observed at this locus and multiple splice variants encoding distinct isoforms are described. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
TGIF1 |
| Location |
18p11.31 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 3412071-3458406 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-TGIF1-20570-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TGIF1-20570-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TGIF1-20570-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TGIF1-20570-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TGIF1-20570-AQ |
467nm |
418nm |
|
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