Gene-specific Copy Number Variation Probe-LOXHD1
Add to Cart
| Catalog: |
CNVFP-LOXHD1-10476 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (LOXHD1). 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: |
LOXHD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to LOXHD1 genes. This product achieves the purpose of detection by hybridizing with the LOXHD1 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 |
Lipoxygenase Homology Domains 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a highly conserved protein consisting entirely of PLAT (polycystin/lipoxygenase/alpha-toxin) domains, thought to be involved in targeting proteins to the plasma membrane. Studies in mice show that this gene is expressed in the mechanosensory hair cells in the inner ear, and mutations in this gene lead to auditory defects, indicating that this gene is essential for normal hair cell function. Screening of human families segregating deafness identified a mutation in this gene which causes DFNB77, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL). Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2010] |
| Gene Symbol |
LOXHD1 |
| Location |
18q21.1 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 44057216-44236996 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-LOXHD1-10476-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-LOXHD1-10476-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-LOXHD1-10476-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-LOXHD1-10476-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-LOXHD1-10476-AQ |
467nm |
418nm |
|
Other Products
