Gene-specific Copy Number Variation Probe-YTHDF2
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| Catalog: |
CNVFP-YTHDF2-23248 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (YTHDF2). 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: |
YTHDF2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to YTHDF2 genes. This product achieves the purpose of detection by hybridizing with the YTHDF2 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 |
YTH N6-methyladenosine RNA Binding Protein 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the YTH (YT521-B homology) superfamily containing YTH domain. The YTH domain is typical for the eukaryotes and is particularly abundant in plants. The YTH domain is usually located in the middle of the protein sequence and may function in binding to RNA. In addition to a YTH domain, this protein has a proline rich region which may be involved in signal transduction. An Alu-rich domain has been identified in one of the introns of this gene, which is thought to be associated with human longevity. In addition, reciprocal translocations between this gene and the Runx1 (AML1) gene on chromosome 21 has been observed in patients with acute myeloid leukemia. This gene was initially mapped to chromosome 14, which was later turned out to be a pseudogene. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Oct 2012] |
| Gene Symbol |
YTHDF2 |
| Location |
1p35.3 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 29063132-29096287 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-YTHDF2-23248-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-YTHDF2-23248-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-YTHDF2-23248-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-YTHDF2-23248-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-YTHDF2-23248-AQ |
467nm |
418nm |
|
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