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Gene-specific Copy Number Variation Probe-TNFRSF13C

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Catalog: CNVFP-TNFRSF13C-21221
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFRSF13C). 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: TNFRSF13C Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFRSF13C genes. This product achieves the purpose of detection by hybridizing with the TNFRSF13C 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 TNF Receptor Superfamily Member 13C
Gene Summary [Provided by RefSeq] B cell-activating factor (BAFF) enhances B-cell survival in vitro and is a regulator of the peripheral B-cell population. Overexpression of Baff in mice results in mature B-cell hyperplasia and symptoms of systemic lupus erythematosus (SLE). Also, some SLE patients have increased levels of BAFF in serum. Therefore, it has been proposed that abnormally high levels of BAFF may contribute to the pathogenesis of autoimmune diseases by enhancing the survival of autoreactive B cells. The protein encoded by this gene is a receptor for BAFF and is a type III transmembrane protein containing a single extracellular cysteine-rich domain. It is thought that this receptor is the principal receptor required for BAFF-mediated mature B-cell survival. [provided by RefSeq, Jul 2008]
Gene Symbol TNFRSF13C
Location 22q13.2
Chromosome Chromosome22
Coordinates This gene maps to 42321035-42322821 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-TNFRSF13C-21221-OR 573nm 548nm
2 RE CNVFP-TNFRSF13C-21221-RE 599nm 580nm
3 GO CNVFP-TNFRSF13C-21221-GO 551nm 525nm
4 GR CNVFP-TNFRSF13C-21221-GR 515nm 491nm
5 AQ CNVFP-TNFRSF13C-21221-AQ 467nm 418nm

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