Gene-specific Copy Number Variation Probe-PHOX2B
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Catalog: |
CNVFP-PHOX2B-15851 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PHOX2B). 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: |
PHOX2B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PHOX2B genes. This product achieves the purpose of detection by hybridizing with the PHOX2B 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 |
Paired Like Homeobox 2b |
Gene Summary [Provided by RefSeq] |
The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins localized to the nucleus. The protein functions as a transcription factor involved in the development of several major noradrenergic neuron populations and the determination of neurotransmitter phenotype. The gene product is linked to enhancement of second messenger-mediated activation of the dopamine beta-hydroylase, c-fos promoters and several enhancers, including cyclic amp-response element and serum-response element. Expansion of a 20 amino acid polyalanine tract in this protein by 5-13 aa has been associated with congenital central hypoventilation syndrome. [provided by RefSeq, Jul 2016] |
Gene Symbol |
PHOX2B |
Location |
4p13 |
Chromosome |
Chromosome4 |
Coordinates |
This gene maps to 41746098-41750987 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-PHOX2B-15851-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PHOX2B-15851-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PHOX2B-15851-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PHOX2B-15851-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PHOX2B-15851-AQ |
467nm |
418nm |
|
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