Gene-specific Copy Number Variation Probe-ALX4
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| Catalog: |
CNVFP-ALX4-00537 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ALX4). 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: |
ALX4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ALX4 genes. This product achieves the purpose of detection by hybridizing with the ALX4 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 |
ALX Homeobox 4 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2); an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism; suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS); a syndrome characterized by craniofacial anomalies, cognitive disability, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart. [provided by RefSeq, Oct 2009] |
| Gene Symbol |
ALX4 |
| Location |
11p11.2 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 44282277-44331716 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-ALX4-00537-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ALX4-00537-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ALX4-00537-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ALX4-00537-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ALX4-00537-AQ |
467nm |
418nm |
|
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