Gene-specific Copy Number Variation Probe-MYT1L
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| Catalog: |
CNVFP-MYT1L-13632 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MYT1L). 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: |
MYT1L Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MYT1L genes. This product achieves the purpose of detection by hybridizing with the MYT1L 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 |
Myelin Transcription Factor 1 Like |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the zinc finger superfamily of transcription factors whose expression, thus far, has been found only in neuronal tissues. The encoded protein belongs to a novel class of cystein-cystein-histidine-cystein zinc finger proteins that function in the developing mammalian central nervous system. Forced expression of this gene in combination with the basic helix-loop-helix transcription factor NeuroD1 and the transcription factors POU class 3 homeobox 2 and achaete-scute family basic helix-loop-helix transcription factor 1 can convert fetal and postnatal human fibroblasts into induced neuronal cells, which are able to generate action potentials. Mutations in this gene have been associated with an autosomal dominant form of cognitive disability and with autism spectrum disorder. Alternative splicing results in multiple variants. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
MYT1L |
| Location |
2p25.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 1792884-2335045 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-MYT1L-13632-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MYT1L-13632-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MYT1L-13632-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MYT1L-13632-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MYT1L-13632-AQ |
467nm |
418nm |
|
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