Gene-specific Copy Number Variation Probe-UMOD
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| Catalog: |
CNVFP-UMOD-22748 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (UMOD). 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: |
UMOD Gene-specific copy number variation probes are mainly used to detect the copy number variation related to UMOD genes. This product achieves the purpose of detection by hybridizing with the UMOD 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 |
Uromodulin |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is the most abundant protein in mammalian urine under physiological conditions. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. This protein may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of this protein in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the renal disorders medullary cystic kidney disease-2 (MCKD2), glomerulocystic kidney disease with hyperuricemia and isosthenuria (GCKDHI), and familial juvenile hyperuricemic nephropathy (FJHN). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
UMOD |
| Location |
16p12.3 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 20344372-20364037 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-UMOD-22748-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-UMOD-22748-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-UMOD-22748-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-UMOD-22748-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-UMOD-22748-AQ |
467nm |
418nm |
|
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