Gene-specific Copy Number Variation Probe-PHF8
Add to Cart
Catalog: |
CNVFP-PHF8-15561 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PHF8). 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: |
PHF8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PHF8 genes. This product achieves the purpose of detection by hybridizing with the PHF8 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 8 |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. The protein has an N-terminal PHD finger and a central Jumonji C domain. This gene is thought to function as a transcription activator. Defects in this gene are a cause of syndromic X-linked Siderius type intellectual disability (MRXSSD) and over-expression of this gene is associated with several forms of cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017] |
Gene Symbol |
PHF8 |
Location |
Xp11.22 |
Chromosome |
ChromosomeX |
Coordinates |
This gene maps to 53963112-54071569 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-PHF8-15561-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PHF8-15561-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PHF8-15561-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PHF8-15561-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PHF8-15561-AQ |
467nm |
418nm |
|
Other Products