Gene-specific Copy Number Variation Probe-PHF7
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Catalog: |
CNVFP-PHF7-15524 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PHF7). 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: |
PHF7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PHF7 genes. This product achieves the purpose of detection by hybridizing with the PHF7 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 7 |
Gene Summary [Provided by RefSeq] |
Spermatogenesis is a complex process regulated by extracellular and intracellular factors as well as cellular interactions among interstitial cells of the testis, Sertoli cells, and germ cells. This gene is expressed in the testis in Sertoli cells but not germ cells. The protein encoded by this gene contains plant homeodomain (PHD) finger domains, also known as leukemia associated protein (LAP) domains, believed to be involved in transcriptional regulation. The protein, which localizes to the nucleus of transfected cells, has been implicated in the transcriptional regulation of spermatogenesis. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013] |
Gene Symbol |
PHF7 |
Location |
3p21.1 |
Chromosome |
Chromosome3 |
Coordinates |
This gene maps to 52444526-52457657 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-PHF7-15524-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PHF7-15524-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PHF7-15524-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PHF7-15524-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PHF7-15524-AQ |
467nm |
418nm |
|
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