Gene-specific Copy Number Variation Probe-NOD1
Add to Cart
| Catalog: |
CNVFP-NOD1-14218 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NOD1). 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: |
NOD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NOD1 genes. This product achieves the purpose of detection by hybridizing with the NOD1 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 |
Nucleotide Binding Oligomerization Domain Containing 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) family of proteins. The encoded protein plays a role in innate immunity by acting as a pattern-recognition receptor (PRR) that binds bacterial peptidoglycans and initiates inflammation. This protein has also been implicated in the immune response to viral and parasitic infection. Major structural features of this protein include an N-terminal caspase recruitment domain (CARD), a centrally located nucleotide-binding domain (NBD), and 10 tandem leucine-rich repeats (LRRs) in its C terminus. The CARD is involved in apoptotic signaling, LRRs participate in protein-protein interactions, and mutations in the NBD may affect the process of oligomerization and subsequent function of the LRR domain. Mutations in this gene are associated with asthma, inflammatory bowel disease, Behcet disease and sarcoidosis in human patients. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
NOD1 |
| Location |
7p14.3 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 30464142-30518393 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-NOD1-14218-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NOD1-14218-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NOD1-14218-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NOD1-14218-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NOD1-14218-AQ |
467nm |
418nm |
|
Other Products
