Gene-specific Copy Number Variation Probe-ALKBH8
Add to Cart
Catalog: |
CNVFP-ALKBH8-00550 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ALKBH8). 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: |
ALKBH8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ALKBH8 genes. This product achieves the purpose of detection by hybridizing with the ALKBH8 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 |
AlkB Homolog 8, TRNA Methyltransferase |
Gene Summary [Provided by RefSeq] |
The AlkB Homolog 8, TRNA Methyltransferase (ALKBH8) gene is located on chr11:107373452 -107436461 at 11q22.3. |
Gene Symbol |
ALKBH8 |
Location |
11q22.3 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 107373452-107436461 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-ALKBH8-00550-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-ALKBH8-00550-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-ALKBH8-00550-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-ALKBH8-00550-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-ALKBH8-00550-AQ |
467nm |
418nm |
|
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