Gene-specific Copy Number Variation Probe-RFX5
Add to Cart
| Catalog: |
CNVFP-RFX5-17149 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RFX5). 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: |
RFX5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RFX5 genes. This product achieves the purpose of detection by hybridizing with the RFX5 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 X5 |
| Gene Summary [Provided by RefSeq] |
A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX, a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al., 1995). RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. Multiple alternatively spliced transcript variants have been found but the full-length natures of only two have been determined. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
RFX5 |
| Location |
1q21.3 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 151313115-151319769 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-RFX5-17149-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RFX5-17149-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RFX5-17149-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RFX5-17149-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RFX5-17149-AQ |
467nm |
418nm |
|
Other Products
