Gene-specific Copy Number Variation Probe-SPART
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| Catalog: |
CNVFP-SPART-19724 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPART). 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: |
SPART Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPART genes. This product achieves the purpose of detection by hybridizing with the SPART 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 |
Spartin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008] |
| Gene Symbol |
SPART |
| Location |
13q13.3 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 36370179-36301637 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-SPART-19724-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SPART-19724-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SPART-19724-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SPART-19724-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SPART-19724-AQ |
467nm |
418nm |
|
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