Gene-specific Copy Number Variation Probe-PHF6
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Catalog: |
CNVFP-PHF6-15529 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PHF6). 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: |
PHF6 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PHF6 genes. This product achieves the purpose of detection by hybridizing with the PHF6 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 |
PHD Finger Protein 6 |
Gene Summary [Provided by RefSeq] |
This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010] |
Gene Symbol |
PHF6 |
Location |
Xq26.2 |
Chromosome |
ChromosomeX |
Coordinates |
This gene maps to 133507341-133562822 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-PHF6-15529-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PHF6-15529-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PHF6-15529-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PHF6-15529-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PHF6-15529-AQ |
467nm |
418nm |
|
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