Gene-specific Copy Number Variation Probe-RFXANK
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| Catalog: |
CNVFP-RFXANK-17143 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RFXANK). 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: |
RFXANK Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RFXANK genes. This product achieves the purpose of detection by hybridizing with the RFXANK 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 |
Regulatory Factor X Associated Ankyrin Containing Protein |
| Gene Summary [Provided by RefSeq] |
Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. This protein contains ankyrin repeats involved in protein-protein interactions. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group B. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
RFXANK |
| Location |
19p13.11 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 19303007-19312678 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-RFXANK-17143-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RFXANK-17143-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RFXANK-17143-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RFXANK-17143-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RFXANK-17143-AQ |
467nm |
418nm |
|
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