Gene-specific Copy Number Variation Probe-KLHL3
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| Catalog: |
CNVFP-KLHL3-08269 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KLHL3). 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: |
KLHL3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KLHL3 genes. This product achieves the purpose of detection by hybridizing with the KLHL3 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 |
Kelch Like Family Member 3 |
| Gene Summary [Provided by RefSeq] |
This gene is ubiquitously expressed and encodes a full-length protein which has an N-terminal BTB domain followed by a BACK domain and six kelch-like repeats in the C-terminus. These kelch-like repeats promote substrate ubiquitination of bound proteins via interaction of the BTB domain with the CUL3 (cullin 3) component of a cullin-RING E3 ubiquitin ligase (CRL) complex. Muatations in this gene cause pseudohypoaldosteronism type IID (PHA2D); a rare Mendelian syndrome featuring hypertension, hyperkalaemia and metabolic acidosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2012] |
| Gene Symbol |
KLHL3 |
| Location |
5q31.2 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 136953188-137071779 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-KLHL3-08269-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KLHL3-08269-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KLHL3-08269-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KLHL3-08269-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KLHL3-08269-AQ |
467nm |
418nm |
|
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