Gene-specific Copy Number Variation Probe-KCTD21
Add to Cart
Catalog: |
CNVFP-KCTD21-08085 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCTD21). 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: |
KCTD21 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCTD21 genes. This product achieves the purpose of detection by hybridizing with the KCTD21 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 |
Potassium Channel Tetramerization Domain Containing 21 |
Gene Summary [Provided by RefSeq] |
The Potassium Channel Tetramerization Domain Containing 21 (KCTD21) gene is located on chr11:77882297 -77899664 at 11q14.1. |
Gene Symbol |
KCTD21 |
Location |
11q14.1 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 77882297-77899664 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-KCTD21-08085-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-KCTD21-08085-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-KCTD21-08085-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-KCTD21-08085-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-KCTD21-08085-AQ |
467nm |
418nm |
|
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