Gene-specific Copy Number Variation Probe-CHM
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| Catalog: |
CNVFP-CHM-02645 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CHM). 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: |
CHM Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CHM genes. This product achieves the purpose of detection by hybridizing with the CHM 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 |
CHM, Rab Escort Protein 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes component A of the RAB geranylgeranyl transferase holoenzyme. In the dimeric holoenzyme, this subunit binds unprenylated Rab GTPases and then presents them to the catalytic Rab GGTase subunit for the geranylgeranyl transfer reaction. Rab GTPases need to be geranylgeranyled on either one or two cysteine residues in their C-terminus to localize to the correct intracellular membrane. Mutations in this gene are a cause of choroideremia; also known as tapetochoroidal dystrophy (TCD). This X-linked disease is characterized by progressive dystrophy of the choroid, retinal pigment epithelium and retina. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016] |
| Gene Symbol |
CHM |
| Location |
Xq21.2 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 85116184-85302566 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-CHM-02645-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CHM-02645-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CHM-02645-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CHM-02645-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CHM-02645-AQ |
467nm |
418nm |
|
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