Gene-specific Copy Number Variation Probe-HAX1
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| Catalog: |
CNVFP-HAX1-06529 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HAX1). 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: |
HAX1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HAX1 genes. This product achieves the purpose of detection by hybridizing with the HAX1 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 |
HCLS1 Associated Protein X-1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
HAX1 |
| Location |
1q21.3 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 154245038-154248355 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-HAX1-06529-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HAX1-06529-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HAX1-06529-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HAX1-06529-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HAX1-06529-AQ |
467nm |
418nm |
|
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