Gene-specific Copy Number Variation Probe-CLDN19
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| Catalog: |
CNVFP-CLDN19-02762 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CLDN19). 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: |
CLDN19 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CLDN19 genes. This product achieves the purpose of detection by hybridizing with the CLDN19 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 |
Claudin 19 |
| Gene Summary [Provided by RefSeq] |
The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010] |
| Gene Symbol |
CLDN19 |
| Location |
1p34.2 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 43198763-43205925 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-CLDN19-02762-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CLDN19-02762-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CLDN19-02762-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CLDN19-02762-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CLDN19-02762-AQ |
467nm |
418nm |
|
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