Gene-specific Copy Number Variation Probe-EML1
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| Catalog: |
CNVFP-EML1-04581 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (EML1). 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: |
EML1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to EML1 genes. This product achieves the purpose of detection by hybridizing with the EML1 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 |
Echinoderm Microtubule Associated Protein Like 1 |
| Gene Summary [Provided by RefSeq] |
Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
EML1 |
| Location |
14q32.2 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 100259744-100408395 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-EML1-04581-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-EML1-04581-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-EML1-04581-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-EML1-04581-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-EML1-04581-AQ |
467nm |
418nm |
|
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