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| Catalog: | GBAFP-KAZALD1-13268 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (KAZALD1). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent. |
| Application: | KAZALD1 Gene-specific Break Apart Probe is designed to detect potential KAZALD1 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services. |
| Quantity: | 20 Tests |
| Probe Kits Volume (µL): | 40 μL |
| Hybridization Solution (µL): | 200 μL |
| Turnaround Time: | Within 10 Business Days |
| Shipping Time: | 1-2 Day Expedited Shipping |
| Shipping Conditions: | -20℃ |
| Storage Conditions: | Store at -20℃ and avoid light; |
| 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 |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-KAZALD1-13268-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-KAZALD1-13268-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-KAZALD1-13268-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-KAZALD1-13268-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-KAZALD1-13268-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-KAZALD1-13268-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-KAZALD1-13268-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-KAZALD1-13268-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-KAZALD1-13268-REGR | 599nm;515nm | 580nm;491nm |
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