Gene-specific Copy Number Variation Probe-KAZALD1
Add to Cart
| Catalog: |
CNVFP-KAZALD1-07862 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KAZALD1). 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: |
KAZALD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KAZALD1 genes. This product achieves the purpose of detection by hybridizing with the KAZALD1 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 |
Kazal Type Serine Peptidase Inhibitor Domain 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a secreted member of the insulin growth factor-binding protein (IGFBP) superfamily. The protein contains an insulin growth factor-binding domain in its N-terminal region, a Kazal-type serine protease inhibitor and follistatin-like domain in its central region, and an immunoglobulin-like domain in its C-terminal region. Studies of the mouse ortholog suggest that this protein may function in bone development and bone regeneration. This gene is hypomethylated and over-expressed in high-grade glioma compared to low-grade glioma, and thus the hypomethylated gene may be associated with cell proliferation and the shorter survival of patients with high-grade glioma. It is also one of numerous genes found to be deleted in a novel 5.54 Mb interstitial deletion, which is associated with multiple congenital anomalies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
| Gene Symbol |
KAZALD1 |
| Location |
10q24.31 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 102820998-102825351 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-KAZALD1-07862-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KAZALD1-07862-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KAZALD1-07862-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KAZALD1-07862-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KAZALD1-07862-AQ |
467nm |
418nm |
|
Other Products
