Gene-specific Copy Number Variation Probe-IGLL1
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| Catalog: |
CNVFP-IGLL1-07225 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (IGLL1). 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: |
IGLL1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to IGLL1 genes. This product achieves the purpose of detection by hybridizing with the IGLL1 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 |
Immunoglobulin Lambda Like Polypeptide 1 |
| Gene Summary [Provided by RefSeq] |
The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
IGLL1 |
| Location |
22q11.23 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 23915312-23922495 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-IGLL1-07225-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-IGLL1-07225-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-IGLL1-07225-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-IGLL1-07225-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-IGLL1-07225-AQ |
467nm |
418nm |
|
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