Gene-specific Copy Number Variation Probe-BTNL2
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| Catalog: |
CNVFP-BTNL2-01659 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BTNL2). 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: |
BTNL2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BTNL2 genes. This product achieves the purpose of detection by hybridizing with the BTNL2 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 |
Butyrophilin Like 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017] |
| Gene Symbol |
BTNL2 |
| Location |
6p21.32 |
| Chromosome |
Chromosome6_mann_hap4 |
| Coordinates |
This gene maps to 3705348-3717760 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-BTNL2-01659-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BTNL2-01659-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BTNL2-01659-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BTNL2-01659-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BTNL2-01659-AQ |
467nm |
418nm |
|
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