Gene-specific Copy Number Variation Probe-PCDH11X
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Catalog: |
CNVFP-PCDH11X-15207 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PCDH11X). 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: |
PCDH11X Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PCDH11X genes. This product achieves the purpose of detection by hybridizing with the PCDH11X 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 |
Protocadherin 11 X-linked |
Gene Summary [Provided by RefSeq] |
This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014] |
Gene Symbol |
PCDH11X |
Location |
Xq21.31 |
Chromosome |
ChromosomeX |
Coordinates |
This gene maps to 91089658-91878228 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-PCDH11X-15207-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PCDH11X-15207-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PCDH11X-15207-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PCDH11X-15207-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PCDH11X-15207-AQ |
467nm |
418nm |
|
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